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{{Infobox_gene}}
{{Infobox_gene}}
'''Xist''' (X-inactive specific transcript) is an [[Non-coding RNA|RNA gene]] on the [[X chromosome]] of the [[Eutheria|placental mammals]] that acts as a major effector of the [[X inactivation]] process.<ref name="entrez_7503">{{cite web | title = Entrez Gene: XIST X (inactive)-specific transcript| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7503| accessdate = }}</ref> It is a component of the [[X-inactivation#Chromosomal component|''Xic'']] - X-chromosome inactivation centre<ref>{{cite journal | vauthors = Chow JC, Yen Z, Ziesche SM, Brown CJ | title = Silencing of the mammalian X chromosome | journal = Annual Review of Genomics and Human Genetics | volume = 6 | issue =  | pages = 69–92 | year = 2005 | pmid = 16124854 | doi = 10.1146/annurev.genom.6.080604.162350 }}</ref> - along with two other RNA genes (''[[Jpx (gene)|Jpx]]'' and ''[[Ftx (gene)|Ftx]]'') and two [[gene|protein genes]] (''Tsx'' and ''Cnbp2'').<ref>{{cite journal | vauthors = Chureau C, Prissette M, Bourdet A, Barbe V, Cattolico L, Jones L, Eggen A, Avner P, Duret L | title = Comparative sequence analysis of the X-inactivation center region in mouse, human, and bovine | journal = Genome Research | volume = 12 | issue = 6 | pages = 894–908 | date = Jun 2002 | pmid = 12045143 | pmc = 1383731 | doi = 10.1101/gr.152902 }}</ref> The Xist RNA, a large (17 kb in humans)<ref name="pmid1423611">{{cite journal | vauthors = Brown CJ, Hendrich BD, Rupert JL, Lafrenière RG, Xing Y, Lawrence J, Willard HF | title = The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus | journal = Cell | volume = 71 | issue = 3 | pages = 527–42 | date = Oct 1992 | pmid = 1423611 | doi = 10.1016/0092-8674(92)90520-M }}</ref> transcript, is expressed on the inactive chromosome and not on the active one. It is processed in a similar way to mRNAs, through [[RNA splicing|splicing]] and [[polyadenylation]]. However, it remains untranslated. It has been suggested that this RNA gene evolved at least partly from a protein coding gene that became a [[pseudogene]].<ref name="Dur09">{{cite journal | vauthors = Duret L, Chureau C, Samain S, Weissenbach J, Avner P | title = The Xist RNA gene evolved in eutherians by pseudogenization of a protein-coding gene | journal = Science | volume = 312 | issue = 5780 | pages = 1653–5 | date = Jun 2006 | pmid = 16778056 | doi = 10.1126/science.1126316 }}</ref> The inactive X chromosome is coated with this transcript, which is essential for the inactivation.<ref>{{cite journal | vauthors = Ng K, Pullirsch D, Leeb M, Wutz A | title = Xist and the order of silencing | journal = EMBO Reports | volume = 8 | issue = 1 | pages = 34–9 | date = Jan 2007 | pmid = 17203100 | pmc = 1796754 | doi = 10.1038/sj.embor.7400871 | format = Review Article | quote = [http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1796754&rendertype=figure&id=f1 Figure 1 Xist RNA encompasses the X from which it is transcribed.] }}</ref> X chromosomes lacking Xist will not be inactivated, while duplication of the Xist gene on another chromosome causes inactivation of that chromosome.<ref>{{cite journal | vauthors = Penny GD, Kay GF, Sheardown SA, Rastan S, Brockdorff N | title = Requirement for Xist in X chromosome inactivation | journal = Nature | volume = 379 | issue = 6561 | pages = 131–7 | date = Jan 1996 | pmid = 8538762 | doi = 10.1038/379131a0 }}</ref>
'''Xist''' (X-inactive specific transcript) is an [[Non-coding RNA|RNA gene]] on the [[X chromosome]] of the [[Eutheria|placental mammals]] that acts as a major effector of the [[X inactivation]] process.<ref name="entrez_7503">{{cite web | title = Entrez Gene: XIST X (inactive)-specific transcript| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7503| access-date = }}</ref> It is a component of the [[X-inactivation#Chromosomal component|''Xic'']] – X-chromosome inactivation centre<ref>{{cite journal | vauthors = Chow JC, Yen Z, Ziesche SM, Brown CJ | title = Silencing of the mammalian X chromosome | journal = Annual Review of Genomics and Human Genetics | volume = 6 | issue =  | pages = 69–92 | year = 2005 | pmid = 16124854 | doi = 10.1146/annurev.genom.6.080604.162350 }}</ref> – along with two other RNA genes (''[[Jpx (gene)|Jpx]]'' and ''[[Ftx (gene)|Ftx]]'') and two [[gene|protein genes]] (''Tsx'' and ''Cnbp2'').<ref>{{cite journal | vauthors = Chureau C, Prissette M, Bourdet A, Barbe V, Cattolico L, Jones L, Eggen A, Avner P, Duret L | title = Comparative sequence analysis of the X-inactivation center region in mouse, human, and bovine | journal = Genome Research | volume = 12 | issue = 6 | pages = 894–908 | date = June 2002 | pmid = 12045143 | pmc = 1383731 | doi = 10.1101/gr.152902 | doi-broken-date = 2018-09-05 }}</ref> The Xist RNA, a large (17 kb in humans)<ref name="pmid1423611">{{cite journal | vauthors = Brown CJ, Hendrich BD, Rupert JL, Lafrenière RG, Xing Y, Lawrence J, Willard HF | title = The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus | journal = Cell | volume = 71 | issue = 3 | pages = 527–42 | date = October 1992 | pmid = 1423611 | doi = 10.1016/0092-8674(92)90520-M }}</ref> transcript, is expressed on the inactive chromosome and not on the active one. It is processed in a similar way to mRNAs, through [[RNA splicing|splicing]] and [[polyadenylation]]. However, it remains untranslated. It has been suggested that this RNA gene evolved at least partly from a protein coding gene that became a [[pseudogene]].<ref name="Dur09">{{cite journal | vauthors = Duret L, Chureau C, Samain S, Weissenbach J, Avner P | title = The Xist RNA gene evolved in eutherians by pseudogenization of a protein-coding gene | journal = Science | volume = 312 | issue = 5780 | pages = 1653–5 | date = June 2006 | pmid = 16778056 | doi = 10.1126/science.1126316 }}</ref> The inactive X chromosome is coated with this transcript, which is essential for the inactivation.<ref>{{cite journal | vauthors = Ng K, Pullirsch D, Leeb M, Wutz A | title = Xist and the order of silencing | journal = EMBO Reports | volume = 8 | issue = 1 | pages = 34–9 | date = January 2007 | pmid = 17203100 | pmc = 1796754 | doi = 10.1038/sj.embor.7400871 | quote = [http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1796754&rendertype=figure&id=f1 Figure 1 Xist RNA encompasses the X from which it is transcribed.] | format = Review Article }}</ref> X chromosomes lacking Xist will not be inactivated, while duplication of the Xist gene on another chromosome causes inactivation of that chromosome.<ref>{{cite journal | vauthors = Penny GD, Kay GF, Sheardown SA, Rastan S, [[Neil Brockdorff|Brockdorff N]] | title = Requirement for Xist in X chromosome inactivation | journal = Nature | volume = 379 | issue = 6561 | pages = 131–7 | year = 1996 | pmid = 8538762 | doi = 10.1038/379131a0 }} {{closed access}}</ref>


== Function ==
== Function ==
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[[X-inactivation|X inactivation]] is an early [[developmental biology|developmental]] process in mammalian females that transcriptionally silences one of the pair of [[X chromosome]]s, thus providing dosage equivalence between males and females (see [[dosage compensation]]). The process is regulated by several factors, including a region of chromosome X called the X inactivation center (XIC). The XIST gene is [[gene expression|expressed]] exclusively from the XIC of the inactive X chromosome. The transcript is [[alternative splicing|spliced]] but apparently does not encode a [[protein]]. The transcript remains in the [[cell nucleus|nucleus]] where it coats the inactive X chromosome. Alternatively spliced transcript variants have been identified, but their full length sequences have not been determined.<ref name="entrez_7503"/>
[[X-inactivation|X inactivation]] is an early [[developmental biology|developmental]] process in mammalian females that transcriptionally silences one of the pair of [[X chromosome]]s, thus providing dosage equivalence between males and females (see [[dosage compensation]]). The process is regulated by several factors, including a region of chromosome X called the X inactivation center (XIC). The XIST gene is [[gene expression|expressed]] exclusively from the XIC of the inactive X chromosome. The transcript is [[alternative splicing|spliced]] but apparently does not encode a [[protein]]. The transcript remains in the [[cell nucleus|nucleus]] where it coats the inactive X chromosome. Alternatively spliced transcript variants have been identified, but their full length sequences have not been determined.<ref name="entrez_7503"/>


The functional role of the Xist transcript was definitively demonstrated in mouse female ES cells using a novel antisense technology, called peptide nucleic acid (PNA) interference mapping.  In the reported experiments, a single 19-bp antisense cell-permeating PNA targeted against a particular region of Xist RNA prevented the formation of  Xi and inhibited cis-silencing of X-linked genes. The association of the Xi with macro-histone H2A is also disturbed by PNA interference mapping.<ref name = "Beletskii_2001">{{cite journal | vauthors = Beletskii A, Hong YK, Pehrson J, Egholm M, Strauss WM | title = PNA interference mapping demonstrates functional domains in the noncoding RNA Xist | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 98 | issue = 16 | pages = 9215–20 | date = Jul 2001 | pmid = 11481485 | pmc = 55400 | doi = 10.1073/pnas.161173098 }}</ref>
The functional role of the Xist transcript was definitively demonstrated in mouse female ES cells using a novel antisense technology, called peptide nucleic acid (PNA) interference mapping.  In the reported experiments, a single 19-bp antisense cell-permeating PNA targeted against a particular region of Xist RNA prevented the formation of  Xi and inhibited cis-silencing of X-linked genes. The association of the Xi with macro-histone H2A is also disturbed by PNA interference mapping.<ref name = "Beletskii_2001">{{cite journal | vauthors = Beletskii A, Hong YK, Pehrson J, Egholm M, Strauss WM | title = PNA interference mapping demonstrates functional domains in the noncoding RNA Xist | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 98 | issue = 16 | pages = 9215–20 | date = July 2001 | pmid = 11481485 | pmc = 55400 | doi = 10.1073/pnas.161173098 }}</ref>


X-inactivation process occurs in mice even in the absence of this gene via [[epigenetics|epigenetic regulation]], but Xist is required to stabilize this silencing.<ref name = "Kalantry_2009">{{cite journal | vauthors = Kalantry S, Purushothaman S, Bowen RB, Starmer J, Magnuson T | title = Evidence of Xist RNA-independent initiation of mouse imprinted X-chromosome inactivation | journal = Nature | volume = 460 | issue = 7255 | pages = 647–51 | date = Jul 2009 | pmid = 19571810 | pmc = 2754729 | doi = 10.1038/nature08161 }}</ref>
X-inactivation process occurs in mice even in the absence of this gene via [[epigenetics|epigenetic regulation]], but Xist is required to stabilize this silencing.<ref name = "Kalantry_2009">{{cite journal | vauthors = Kalantry S, Purushothaman S, Bowen RB, Starmer J, Magnuson T | title = Evidence of Xist RNA-independent initiation of mouse imprinted X-chromosome inactivation | journal = Nature | volume = 460 | issue = 7255 | pages = 647–51 | date = July 2009 | pmid = 19571810 | pmc = 2754729 | doi = 10.1038/nature08161 }}</ref>


== Gene location ==
== Gene location ==


The human Xist RNA gene is located on the long (q) arm of the X chromosome. The Xist RNA gene consists of conserved repeats within its structure and is also largely localized in the nucleus.<ref name="pmid1423611" /> The Xist RNA gene consists of an A region, which contains 8 repeats separated by U-rich spacers. The A region appears to contain two long stem-loop structures that each include four repeats.<ref name="pmid20052282">{{cite journal | vauthors = Maenner S, Blaud M, Fouillen L, Savoye A, Marchand V, Dubois A, Sanglier-Cianférani S, Van Dorsselaer A, Clerc P, Avner P, Visvikis A, Branlant C | title = 2-D structure of the A region of Xist RNA and its implication for PRC2 association | journal = PLoS Biology | volume = 8 | issue = 1 | pages = e1000276 | date = Jan 2010 | pmid = 20052282 | pmc = 2796953 | doi = 10.1371/journal.pbio.1000276 | veditors = Hall K }}</ref> An ortholog of the Xist RNA gene in humans has been identified in mice. This ortholog is a 15 kb Xist RNA gene that is also localized in the nucleus. However, the ortholog does not consist of conserved repeats.<ref>{{cite journal | vauthors = Brockdorff N, Ashworth A, Kay GF, McCabe VM, Norris DP, Cooper PJ, Swift S, Rastan S | title = The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus | journal = Cell | volume = 71 | issue = 3 | pages = 515–26 | date = Oct 1992 | pmid = 1423610 | doi = 10.1016/0092-8674(92)90519-I }}</ref> The gene also consists of an Xist Inactivation Center (XIC), which plays a major role in X inactivation.<ref name="Lee JT, Davidow LS, Warshawsk D 1999 400–09">{{cite journal | vauthors = Lee JT, Davidow LS, Warshawsky D | title = Tsix, a gene antisense to Xist at the X-inactivation centre | journal = Nature Genetics | volume = 21 | issue = 4 | pages = 400–4 | date = Apr 1999 | pmid = 10192391 | doi = 10.1038/7734 }}</ref>
The human Xist RNA gene is located on the long (q) arm of the X chromosome. The Xist RNA gene consists of conserved repeats within its structure and is also largely localized in the nucleus.<ref name="pmid1423611" /> The Xist RNA gene consists of an A region, which contains 8 repeats separated by U-rich spacers. The A region appears to contain two long stem-loop structures that each include four repeats.<ref name="pmid20052282">{{cite journal | vauthors = Maenner S, Blaud M, Fouillen L, Savoye A, Marchand V, Dubois A, Sanglier-Cianférani S, Van Dorsselaer A, Clerc P, Avner P, Visvikis A, Branlant C | title = 2-D structure of the A region of Xist RNA and its implication for PRC2 association | journal = PLoS Biology | volume = 8 | issue = 1 | pages = e1000276 | date = January 2010 | pmid = 20052282 | pmc = 2796953 | doi = 10.1371/journal.pbio.1000276 | veditors = Hall K }}</ref> An ortholog of the Xist RNA gene in humans has been identified in mice. This ortholog is a 15 kb Xist RNA gene that is also localized in the nucleus. However, the ortholog does not consist of conserved repeats.<ref>{{cite journal | vauthors = [[Neil Brockdorff|Brockdorff N]], Ashworth A, Kay GF, McCabe VM, Norris DP, Cooper PJ, Swift S, Rastan S | title = The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus | journal = Cell | volume = 71 | issue = 3 | pages = 515–26 | year= 1992 | pmid = 1423610 | doi = 10.1016/0092-8674(92)90519-I }}</ref> The gene also consists of an Xist Inactivation Center (XIC), which plays a major role in X inactivation.<ref name="Lee JT, Davidow LS, Warshawsk D 1999 400–09">{{cite journal | vauthors = Lee JT, Davidow LS, Warshawsky D | title = Tsix, a gene antisense to Xist at the X-inactivation centre | journal = Nature Genetics | volume = 21 | issue = 4 | pages = 400–4 | date = April 1999 | pmid = 10192391 | doi = 10.1038/7734 }}</ref>


== Transcript organization ==
== Transcript organization ==
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=== A region ===
=== A region ===


[[File:RepA Model Xist.png|thumb|Structure model of the repeat A (repA) region of Xist based on in vivo biochemical structure probing and comparative sequence analysis. Repeats 1 to 8(1/2) are numbered and boxed - they are shown in red on the cartoon of repA in the upper left hand panel. Reactive nucleotides are colored red, where open and closed circles are medium and strongly reactive, respectively (reactivity suggests that a nucleotide is unpaired or loosely structured). Consistent and compensatory mutations (single and double point mutations that preserve pairing) are annotated in blue and purple, respectively. Base pairs that are 100% conserved in rodents are bold and black, while those conserved in rodents and mammals are in green. The data and model are taken from {{cite journal |vauthors= Fang R, Moss WN, Rutenberg-Schoenberg M, and Simon M |date=2015 |title=Probing Xist RNA Structure in Cells Using Targeted Structure-Seq |url=http://journals.plos.org/plosgenetics/article?id=10.1371%2Fjournal.pgen.1005668 |journal=PLoS Genetics |publisher= |volume=11 |issue=12 |pages=e1005668 |doi=10.1371/journal.pgen.1005668 |pmc= 4672913|pmid=26646615}}.|300px|right]]
[[File:RepA Model Xist.png|thumb|Structure model of the repeat A (repA) region of Xist based on in vivo biochemical structure probing and comparative sequence analysis. Repeats 1 to 8(1/2) are numbered and boxed - they are shown in red on the cartoon of repA in the upper left hand panel. Reactive nucleotides are colored red, where open and closed circles are medium and strongly reactive, respectively (reactivity suggests that a nucleotide is unpaired or loosely structured). Consistent and compensatory mutations (single and double point mutations that preserve pairing) are annotated in blue and purple, respectively. Base pairs that are 100% conserved in rodents are bold and black, while those conserved in rodents and mammals are in green. The data and model are taken from {{cite journal | vauthors = Fang R, Moss WN, Rutenberg-Schoenberg M, Simon MD | title = Probing Xist RNA Structure in Cells Using Targeted Structure-Seq | journal = PLoS Genetics | volume = 11 | issue = 12 | pages = e1005668 | date = December 2015 | pmid = 26646615 | pmc = 4672913 | doi = 10.1371/journal.pgen.1005668 }}.|300px|right]]


The Xist RNA contains a region of conservation called the repeat A (repA) region that contains up to nine repeated elements.<ref name="pmid20052282"/> It was initially suggested that repA repeats could fold back on themselves to form local intra-repeat [[stem-loop]] structures. Later work using in vitro biochemical structure probing proposed several inter-repeat [[stem-loop]] structures.<ref name="pmid1423611" /><ref name="pmid20052282"/> A recent study using in vivo biochemical probing and comparative sequence analysis proposed a revision of the repA structure model that includes both intra-repeat and inter-repeat folding found in previous models as well as novel features (see Figure). In addition to its agreement with the in vivo data, this revised model is highly conserved in rodents and mammals (including humans) suggesting functional importance for repA structure. Although the exact function of the repA region is uncertain, it was shown that the entire region is needed for efficient binding to the Suz12 protein.<ref name="pmid20052282"/>
The Xist RNA contains a region of conservation called the repeat A (repA) region that contains up to nine repeated elements.<ref name="pmid20052282"/> It was initially suggested that repA repeats could fold back on themselves to form local intra-repeat [[stem-loop]] structures. Later work using in vitro biochemical structure probing proposed several inter-repeat [[stem-loop]] structures.<ref name="pmid1423611" /><ref name="pmid20052282"/> A recent study using in vivo biochemical probing and comparative sequence analysis proposed a revision of the repA structure model that includes both intra-repeat and inter-repeat folding found in previous models as well as novel features (see Figure). In addition to its agreement with the in vivo data, this revised model is highly conserved in rodents and mammals (including humans) suggesting functional importance for repA structure. Although the exact function of the repA region is uncertain, it was shown that the entire region is needed for efficient binding to the Suz12 protein.<ref name="pmid20052282"/>
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== X Inactivation Centre (XIC) ==
== X Inactivation Centre (XIC) ==


The Xist RNA gene lies within the X-Inactivation Centre (XIC), which plays a major role in Xist expression and X inactivation.<ref>{{cite journal | vauthors = Herzing LB, Romer JT, Horn JM, Ashworth A | title = Xist has properties of the X-chromosome inactivation centre | journal = Nature | volume = 386 | issue = 6622 | pages = 272–5 | date = Mar 1997 | pmid = 9069284 | doi = 10.1038/386272a0 }}</ref> The XIC is located on the q arm of the X chromosome (Xq13). XIC regulates Xist in cis X inactivation, where Tsix, an antisense of Xist, downregulates the expression of Xist. The Xist promoter of XIC is the master regulator of X inactivation.<ref name="Lee JT, Davidow LS, Warshawsk D 1999 400–09"/> X inactivation plays a key role in dosage compensation.
The Xist RNA gene lies within the X-Inactivation Centre (XIC), which plays a major role in Xist expression and X inactivation.<ref>{{cite journal | vauthors = Herzing LB, Romer JT, Horn JM, Ashworth A | title = Xist has properties of the X-chromosome inactivation centre | journal = Nature | volume = 386 | issue = 6622 | pages = 272–5 | date = March 1997 | pmid = 9069284 | doi = 10.1038/386272a0 }}</ref> The XIC is located on the q arm of the X chromosome (Xq13). XIC regulates Xist in cis X inactivation, where Tsix, an antisense of Xist, downregulates the expression of Xist. The Xist promoter of XIC is the master regulator of X inactivation.<ref name="Lee JT, Davidow LS, Warshawsk D 1999 400–09"/> X inactivation plays a key role in dosage compensation.


=== Tsix antisense transcript ===
=== Tsix antisense transcript ===


The [[Tsix]] antisense gene is a transcript of the Xist gene at the XIC center.<ref>{{Cite journal|last=Lee|first=J. T.|last2=Davidow|first2=L. S.|last3=Warshawsky|first3=D.|date=April 1999|title=Tsix, a gene antisense to Xist at the X-inactivation centre|url=https://www.ncbi.nlm.nih.gov/pubmed/10192391|journal=Nature Genetics|volume=21|issue=4|pages=400–404|doi=10.1038/7734|issn=1061-4036|pmid=10192391}}</ref> The Tsix antisense transcript acts in [[cis-regulatory element|cis]] to repress the transcription of Xist, which negatively regulates its expression. The mechanism behind how Tsix modulates Xist activity in cis is poorly understood; however, there are a few theories on its mechanism. One theory is that Tsix is involved in [[chromatin]] modification at the Xist locus and another is that [[transcription factor]]s of [[Cell potency#Pluripotency|pluripotent cell]]s play a role in Xist repression.<ref name="Senner CE, Brockdorff N 2009 122–26">{{cite journal | vauthors = Senner CE, Brockdorff N | title = Xist gene regulation at the onset of X inactivation | journal = Current Opinion in Genetics & Development | volume = 19 | issue = 2 | pages = 122–6 | date = Apr 2009 | pmid = 19345091 | doi = 10.1016/j.gde.2009.03.003 }}</ref>
The [[Tsix]] antisense gene is a transcript of the Xist gene at the XIC center.<ref>{{cite journal | vauthors = Lee JT, Davidow LS, Warshawsky D | title = Tsix, a gene antisense to Xist at the X-inactivation centre | journal = Nature Genetics | volume = 21 | issue = 4 | pages = 400–4 | date = April 1999 | pmid = 10192391 | doi = 10.1038/7734 }}</ref> The Tsix antisense transcript acts in [[cis-regulatory element|cis]] to repress the transcription of Xist, which negatively regulates its expression. The mechanism behind how Tsix modulates Xist activity in cis is poorly understood; however, there are a few theories on its mechanism. One theory is that Tsix is involved in [[chromatin]] modification at the Xist locus and another is that [[transcription factor]]s of [[Cell potency#Pluripotency|pluripotent cell]]s play a role in Xist repression.<ref name="Senner CE, Brockdorff N 2009 122–26">{{cite journal | vauthors = Senner CE, Brockdorff N | title = Xist gene regulation at the onset of X inactivation | journal = Current Opinion in Genetics & Development | volume = 19 | issue = 2 | pages = 122–6 | date = April 2009 | pmid = 19345091 | doi = 10.1016/j.gde.2009.03.003 }}</ref>


== Regulation of the Xist promoter ==
== Regulation of the Xist promoter ==
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=== Methylation ===
=== Methylation ===


The Tsix antisense is believed to activate DNA [[methyl transferase]]s that [[DNA methylation|methylate]] the Xist [[gene promoter|promoter]], in return resulting in inhibition of the Xist promoter and thus the expression of the Xist gene.<ref>{{cite journal | vauthors = Nesterova TB, Popova BC, Cobb BS, Norton S, Senner CE, Tang YA, Spruce T, Rodriguez TA, Sado T, Merkenschlager M, Brockdorff N | title = Dicer regulates Xist promoter methylation in ES cells indirectly through transcriptional control of Dnmt3a | journal = Epigenetics & Chromatin | volume = 1 | issue = 1 | pages = 2 | year = 2008 | pmid = 19014663 | pmc = 257704 | doi = 10.1186/1756-8935-1-2 }}</ref> Methylation of histone 3 lysine 4 (H3K4) produces an active chromatin structure, which recruits transcription factors and thus allows for transcription to occur, therefore in this case the transcription of Xist.<ref>{{cite journal | vauthors = Navarro P, Pichard S, Ciaudo C, Avner P, Rougeulle C | title = Tsix transcription across the Xist gene alters chromatin conformation without affecting Xist transcription: implications for X-chromosome inactivation | journal = Genes & Development | volume = 19 | issue = 12 | pages = 1474–84 | date = Jun 2005 | pmid = 15964997 | pmc = 1151664 | doi = 10.1101/gad.341105 }}</ref>
The Tsix antisense is believed to activate DNA [[methyl transferase]]s that [[DNA methylation|methylate]] the Xist [[gene promoter|promoter]], in return resulting in inhibition of the Xist promoter and thus the expression of the Xist gene.<ref>{{cite journal | vauthors = Nesterova TB, Popova BC, Cobb BS, Norton S, Senner CE, Tang YA, Spruce T, Rodriguez TA, Sado T, Merkenschlager M, Brockdorff N | title = Dicer regulates Xist promoter methylation in ES cells indirectly through transcriptional control of Dnmt3a | journal = [[Epigenetics & Chromatin]] | volume = 1 | issue = 1 | pages = 2 | date = October 2008 | pmid = 19014663 | pmc = 257704 | doi = 10.1186/1756-8935-1-2 }}</ref> Methylation of histone 3 lysine 4 (H3K4) produces an active chromatin structure, which recruits transcription factors and thus allows for transcription to occur, therefore in this case the transcription of Xist.<ref>{{cite journal | vauthors = Navarro P, Pichard S, Ciaudo C, Avner P, Rougeulle C | title = Tsix transcription across the Xist gene alters chromatin conformation without affecting Xist transcription: implications for X-chromosome inactivation | journal = Genes & Development | volume = 19 | issue = 12 | pages = 1474–84 | date = June 2005 | pmid = 15964997 | pmc = 1151664 | doi = 10.1101/gad.341105 }}</ref>


=== dsRNA and RNAi ===
=== dsRNA and RNAi ===


A [[dsRNA]] and [[RNAi]] pathway have been also proposed to play a role in regulation of the Xist Promoter. [[Dicer]] is an RNAi enzyme and it is believed to cleave the duplex of Xist and Tsix at the beginning of X inactivation, to small ~30 nucleotide RNAs, which have been termed xiRNAs, These xiRNAs are believed to be involved in repressing Xist on the probable active X chromosome based upon studies. A study was conducted where normal endogenous Dicer levels were decreased to 5%, which led to an increase in Xist expression in undifferentiated cells, thus supporting the role of xiRNAs in Xist repression.<ref>{{cite journal | vauthors = Ogawa Y, Sun BK, Lee JT | title = Intersection of the RNA interference and X-inactivation pathways | journal = Science | volume = 320 | issue = 5881 | pages = 1336–41 | date = Jun 2008 | pmid = 18535243 | pmc = 2584363 | doi = 10.1126/science.1157676 }}</ref> The role and mechanism of xiRNAs is still under examination and debate.{{Citation needed|date=April 2011}}
A [[dsRNA]] and [[RNAi]] pathway have been also proposed to play a role in regulation of the Xist Promoter. [[Dicer]] is an RNAi enzyme and it is believed to cleave the duplex of Xist and Tsix at the beginning of X inactivation, to small ~30 nucleotide RNAs, which have been termed xiRNAs, These xiRNAs are believed to be involved in repressing Xist on the probable active X chromosome based upon studies. A study was conducted where normal endogenous Dicer levels were decreased to 5%, which led to an increase in Xist expression in undifferentiated cells, thus supporting the role of xiRNAs in Xist repression.<ref>{{cite journal | vauthors = Ogawa Y, Sun BK, Lee JT | title = Intersection of the RNA interference and X-inactivation pathways | journal = Science | volume = 320 | issue = 5881 | pages = 1336–41 | date = June 2008 | pmid = 18535243 | pmc = 2584363 | doi = 10.1126/science.1157676 }}</ref> The role and mechanism of xiRNAs is still under examination and debate.{{Citation needed|date=April 2011}}


=== Tsix independent mechanisms ===
=== Tsix independent mechanisms ===
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==== Pluripotent cell transcriptional factors ====
==== Pluripotent cell transcriptional factors ====


[[Pluripotent stem cell]]s express transcription factors [[Nanog]], [[Oct4]] and [[Sox2]] that seem to play a role in repressing Xist. In the absence of Tsix in pluripotent cells, Xist is repressed, where a mechanism has been proposed that these transcription factors cause splicing to occur at [[intron]] 1 at the binding site of these factors on the Xist gene, which inhibits Xist expression<ref name="Senner CE, Brockdorff N 2009 122–26"/> A study was conducted where Nanog or Oct4 transcription factors were depleted in pluripotent cells, which resulted in the upregulation of Xist. From this study, it is proposed that Nanog and Oct4 are involved in the repression of Xist expression.<ref>{{cite journal | vauthors = Navarro P, Chambers I, Karwacki-Neisius V, Chureau C, Morey C, Rougeulle C, Avner P | title = Molecular coupling of Xist regulation and pluripotency | journal = Science | volume = 321 | issue = 5896 | pages = 1693–5 | date = Sep 2008 | pmid = 18802003 | doi = 10.1126/science.1160952 }}</ref>
[[Pluripotent stem cell]]s express transcription factors [[Homeobox protein NANOG|Nanog]], [[Oct4]] and [[Sox2]] that seem to play a role in repressing Xist. In the absence of Tsix in pluripotent cells, Xist is repressed, where a mechanism has been proposed that these transcription factors cause splicing to occur at [[intron]] 1 at the binding site of these factors on the Xist gene, which inhibits Xist expression<ref name="Senner CE, Brockdorff N 2009 122–26"/> A study was conducted where Nanog or Oct4 transcription factors were depleted in pluripotent cells, which resulted in the upregulation of Xist. From this study, it is proposed that Nanog and Oct4 are involved in the repression of Xist expression.<ref>{{cite journal | vauthors = Navarro P, Chambers I, Karwacki-Neisius V, Chureau C, Morey C, Rougeulle C, Avner P | title = Molecular coupling of Xist regulation and pluripotency | journal = Science | volume = 321 | issue = 5896 | pages = 1693–5 | date = September 2008 | pmid = 18802003 | doi = 10.1126/science.1160952 }}</ref>


==== Polycomb repressive complex ====
==== Polycomb repressive complex ====


Polycomb repressive complex 2 ([[PRC2]]) consist of a class of polycomb group proteins that are involved in catalyzing the trimethylation of [[histone H3]] on [[lysine]] 27 (K27), which results in chromatin repression, and thus leads to transcriptional silencing. Xist RNA recruits polycomb complexes to the inactive X chromosome at the onset of XCI.<ref>{{Cite journal|last=Zhao|first=Jing|last2=Sun|first2=Bryan K.|last3=Erwin|first3=Jennifer A.|last4=Song|first4=Ji-Joon|last5=Lee|first5=Jeannie T.|date=2008-10-31|title=Polycomb proteins targeted by a short repeat RNA to the mouse X chromosome|url=https://www.ncbi.nlm.nih.gov/pubmed/18974356|journal=Science|volume=322|issue=5902|pages=750–756|doi=10.1126/science.1163045|issn=1095-9203|pmc=2748911|pmid=18974356}}</ref> [[SUZ12]] is a component of the PRC2 and contains a [[zinc finger]] domain. The zinc finger domain is believed to bind to the RNA molecule.<ref>{{cite journal | vauthors = de Napoles M, Mermoud JE, Wakao R, Tang YA, Endoh M, Appanah R, Nesterova TB, Silva J, Otte AP, Vidal M, Koseki H, Brockdorff N | title = Polycomb group proteins Ring1A/B link ubiquitylation of histone H2A to heritable gene silencing and X inactivation | journal = Developmental Cell | volume = 7 | issue = 5 | pages = 663–76 | date = Nov 2004 | pmid = 15525528 | doi = 10.1016/j.devcel.2004.10.005 }}</ref> The PRC2 has been observed to repress Xist expression independent of the Tsix antisense transcript, although the definite mechanism is still not known.
Polycomb repressive complex 2 ([[PRC2]]) consist of a class of polycomb group proteins that are involved in catalyzing the trimethylation of [[histone H3]] on [[lysine]] 27 (K27), which results in chromatin repression, and thus leads to transcriptional silencing. Xist RNA recruits polycomb complexes to the inactive X chromosome at the onset of XCI.<ref>{{cite journal | vauthors = Zhao J, Sun BK, Erwin JA, Song JJ, Lee JT | title = Polycomb proteins targeted by a short repeat RNA to the mouse X chromosome | journal = Science | volume = 322 | issue = 5902 | pages = 750–6 | date = October 2008 | pmid = 18974356 | pmc = 2748911 | doi = 10.1126/science.1163045 }}</ref> [[SUZ12]] is a component of the PRC2 and contains a [[zinc finger]] domain. The zinc finger domain is believed to bind to the RNA molecule.<ref>{{cite journal | vauthors = de Napoles M, Mermoud JE, Wakao R, Tang YA, Endoh M, Appanah R, Nesterova TB, Silva J, Otte AP, Vidal M, Koseki H, [[Neil Brockdorff|Brockdorff N]] | title = Polycomb group proteins Ring1A/B link ubiquitylation of histone H2A to heritable gene silencing and X inactivation | journal = Developmental Cell | volume = 7 | issue = 5 | pages = 663–76 | year = 2004 | pmid = 15525528 | doi = 10.1016/j.devcel.2004.10.005 }}</ref> The PRC2 has been observed to repress Xist expression independent of the Tsix antisense transcript, although the definite mechanism is still not known.


== Dosage compensation ==
== Dosage compensation ==


X inactivation plays a key role in [[dosage compensation]] mechanisms that allow for equal expression of the X and autosomal chromosomes.<ref name="ReferenceA">{{cite journal | vauthors = Nguyen DK, Disteche CM | title = Dosage compensation of the active X chromosome in mammals | journal = Nature Genetics | volume = 38 | issue = 1 | pages = 47–53 | date = Jan 2006 | pmid = 16341221 | doi = 10.1038/ng1705 }}</ref> Different species have different dosage compensation methods, with all of the methods involving the regulation of an X chromosome from one of the either sexes.<ref name="ReferenceA"/> Some methods involved in dosage compensation to inactivate one of the X chromosomes from one of the sexes are Tsix antisense gene, DNA methylation and DNA acetylation;<ref>{{cite journal | vauthors = Csankovszki G, Nagy A, Jaenisch R | title = Synergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivation | journal = The Journal of Cell Biology | volume = 153 | issue = 4 | pages = 773–84 | date = May 2001 | pmid = 11352938 | pmc = 2192370 | doi = 10.1083/jcb.153.4.773 }}</ref> however, the definite mechanism of X inactivation is still poorly understood. If one of the X chromosomes is not inactivated or is partially expressed, it could lead to over expression of the X chromosome and it could be lethal in some cases.
X inactivation plays a key role in [[dosage compensation]] mechanisms that allow for equal expression of the X and autosomal chromosomes.<ref name="ReferenceA">{{cite journal | vauthors = Nguyen DK, Disteche CM | title = Dosage compensation of the active X chromosome in mammals | journal = Nature Genetics | volume = 38 | issue = 1 | pages = 47–53 | date = January 2006 | pmid = 16341221 | doi = 10.1038/ng1705 }}</ref> Different species have different dosage compensation methods, with all of the methods involving the regulation of an X chromosome from one of the either sexes.<ref name="ReferenceA"/> Some methods involved in dosage compensation to inactivate one of the X chromosomes from one of the sexes are Tsix antisense gene, DNA methylation and DNA acetylation;<ref>{{cite journal | vauthors = Csankovszki G, Nagy A, Jaenisch R | title = Synergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivation | journal = The Journal of Cell Biology | volume = 153 | issue = 4 | pages = 773–84 | date = May 2001 | pmid = 11352938 | pmc = 2192370 | doi = 10.1083/jcb.153.4.773 }}</ref> however, the definite mechanism of X inactivation is still poorly understood. If one of the X chromosomes is not inactivated or is partially expressed, it could lead to over expression of the X chromosome and it could be lethal in some cases.


[[Turner's syndrome|Turner's Syndrome]] is one example of where dosage compensation does not equally express the X chromosome, and in females one of the X chromosomes is missing or has abnormalities, which leads to physical abnormalities and also gonadal dysfunction in females due to the one missing or abnormal X chromosome. Turner's syndrome is also referred to as a monosomy X condition.<ref>{{cite journal |vauthors=Chenga MK, Nguyena KD, Disteche CM |year=2006 |title=Dosage compensation of the X chromosome and Turner syndrome=International-Congress-series|volume=1298|pages=3–8 |doi=10.1016/j.ics.2006.06.012}}</ref>
[[Turner's syndrome|Turner's Syndrome]] is one example of where dosage compensation does not equally express the X chromosome, and in females one of the X chromosomes is missing or has abnormalities, which leads to physical abnormalities and also gonadal dysfunction in females due to the one missing or abnormal X chromosome. Turner's syndrome is also referred to as a monosomy X condition.<ref>{{cite journal |vauthors=Chenga MK, Nguyena KD, Disteche CM |year=2006 |title=Dosage compensation of the X chromosome and Turner syndrome=International-Congress-series|journal=International Congress Series |volume=1298|pages=3–8 |doi=10.1016/j.ics.2006.06.012}}</ref>


== X inactivation cycle ==
== X inactivation cycle ==


Xist expression and X inactivation change throughout embryonic development. In early embryogenesis, the [[oocyte]] and sperm do not express Xist and the X chromosome remains active. After fertilization, when the cells are in the 2 to 4 cell stage, Xist transcripts are expressed randomly from one X chromosome in every cell, causing that X chromosome to become imprinted and inactivated. The cells develop into [[Pluripotent|pluripotent cells]] (the inner cell mass) where the imprint is removed, which leads to the downregulation of Xist and thus reactivation of the inactive X chromosome. Recent data suggests that Xist activity is regulated by an anti-sense transcript.<ref>{{cite journal | vauthors = Mak W, Nesterova TB, de Napoles M, Appanah R, Yamanaka S, Otte AP, Brockdorff N | title = Reactivation of the paternal X chromosome in early mouse embryos | journal = Science | volume = 303 | issue = 5658 | pages = 666–9 | date = Jan 2004 | pmid = 14752160 | doi = 10.1126/science.1092674 }}</ref> The [[epiblast]] cells are then formed and they begin to differentiate, and the Xist is upregulated from either of the two X chromosomes and at random, an X is inactivated and the Xist allele is turned off in the active X chromosome. In maturing XX primordial germ cells, Xist is downregulated and X reactivation occurs once again.<ref>{{cite journal | vauthors = Nesterova TB, Mermoud JE, Hilton K, Pehrson J, Surani MA, McLaren A, Brockdorff N | title = Xist expression and macroH2A1.2 localisation in mouse primordial and pluripotent embryonic germ cells | journal = Differentiation; Research in Biological Diversity | volume = 69 | issue = 4–5 | pages = 216–25 | date = Jan 2002 | pmid = 11841480 | doi = 10.1046/j.1432-0436.2002.690415.x }}</ref>
Xist expression and X inactivation change throughout embryonic development. In early embryogenesis, the [[oocyte]] and sperm do not express Xist and the X chromosome remains active. After fertilization, when the cells are in the 2 to 4 cell stage, Xist transcripts are expressed from parent X chromosome(Xp) in every cell, causing that X chromosome to become imprinted and inactivated. Some cells develop into [[Pluripotent|pluripotent cells]] (the inner cell mass) when the blastocyte forms. There, the imprint is removed, leading to the downregulation of Xist and thus reactivation of the inactive X chromosome. Recent data suggests that Xist activity is regulated by an anti-sense transcript.<ref>{{cite journal | vauthors = Mak W, Nesterova TB, de Napoles M, Appanah R, Yamanaka S, Otte AP, Brockdorff N | title = Reactivation of the paternal X chromosome in early mouse embryos | journal = Science | volume = 303 | issue = 5658 | pages = 666–9 | date = January 2004 | pmid = 14752160 | doi = 10.1126/science.1092674 }}</ref> The [[epiblast]] cells are then formed and they begin to be differentiated, and the Xist is upregulated from either of the two X chromosomes and at random in '''ICM''', but the Xist is maintained in epiblast, an X is inactivated and the Xist allele is turned off in the active X chromosome. In maturing XX primordial germ cells, Xist is downregulated and X reactivation occurs once again.<ref>{{cite journal | vauthors = Nesterova TB, Mermoud JE, Hilton K, Pehrson J, Surani MA, McLaren A, Brockdorff N | title = Xist expression and macroH2A1.2 localisation in mouse primordial and pluripotent embryonic germ cells | journal = Differentiation; Research in Biological Diversity | volume = 69 | issue = 4–5 | pages = 216–25 | date = January 2002 | pmid = 11841480 | doi = 10.1046/j.1432-0436.2002.690415.x }}</ref>


== Disease linkage ==
== Disease linkage ==
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== Interactions ==
== Interactions ==


XIST (gene) has been shown to [[Protein-protein interaction|interact]] with [[BRCA1]].<ref name="pmid15065664">{{cite journal | vauthors = Ganesan S, Silver DP, Drapkin R, Greenberg R, Feunteun J, Livingston DM | title = Association of BRCA1 with the inactive X chromosome and XIST RNA | journal = Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences | volume = 359 | issue = 1441 | pages = 123–8 | date = Jan 2004 | pmid = 15065664 | pmc = 1693294 | doi = 10.1098/rstb.2003.1371 }}</ref><ref name="pmid12419249">{{cite journal | vauthors = Ganesan S, Silver DP, Greenberg RA, Avni D, Drapkin R, Miron A, Mok SC, Randrianarison V, Brodie S, Salstrom J, Rasmussen TP, Klimke A, Marrese C, Marahrens Y, Deng CX, Feunteun J, Livingston DM | title = BRCA1 supports XIST RNA concentration on the inactive X chromosome | journal = Cell | volume = 111 | issue = 3 | pages = 393–405 | date = Nov 2002 | pmid = 12419249 | doi = 10.1016/S0092-8674(02)01052-8 }}</ref>
XIST (gene) has been shown to [[Protein-protein interaction|interact]] with [[BRCA1]].<ref name="pmid15065664">{{cite journal | vauthors = Ganesan S, Silver DP, Drapkin R, Greenberg R, Feunteun J, Livingston DM | title = Association of BRCA1 with the inactive X chromosome and XIST RNA | journal = Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences | volume = 359 | issue = 1441 | pages = 123–8 | date = January 2004 | pmid = 15065664 | pmc = 1693294 | doi = 10.1098/rstb.2003.1371 }}</ref><ref name="pmid12419249">{{cite journal | vauthors = Ganesan S, Silver DP, Greenberg RA, Avni D, Drapkin R, Miron A, Mok SC, Randrianarison V, Brodie S, Salstrom J, Rasmussen TP, Klimke A, Marrese C, Marahrens Y, Deng CX, Feunteun J, Livingston DM | title = BRCA1 supports XIST RNA concentration on the inactive X chromosome | journal = Cell | volume = 111 | issue = 3 | pages = 393–405 | date = November 2002 | pmid = 12419249 | doi = 10.1016/S0092-8674(02)01052-8 }}</ref>


== See also ==
== See also ==
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== Further reading ==
== Further reading ==
{{Refbegin|33em}}
{{Refbegin|33em}}
* {{cite journal | vauthors = Brown CJ, Ballabio A, Rupert JL, Lafreniere RG, Grompe M, Tonlorenzi R, Willard HF | title = A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome | journal = Nature | volume = 349 | issue = 6304 | pages = 38–44 | date = Jan 1991 | pmid = 1985261 | doi = 10.1038/349038a0 }}
* {{cite journal | vauthors = Brown CJ, Ballabio A, Rupert JL, Lafreniere RG, Grompe M, Tonlorenzi R, Willard HF | title = A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome | journal = Nature | volume = 349 | issue = 6304 | pages = 38–44 | date = January 1991 | pmid = 1985261 | doi = 10.1038/349038a0 }}
* {{cite journal | vauthors = Brown CJ, Lafreniere RG, Powers VE, Sebastio G, Ballabio A, Pettigrew AL, Ledbetter DH, Levy E, Craig IW, Willard HF | title = Localization of the X inactivation centre on the human X chromosome in Xq13 | journal = Nature | volume = 349 | issue = 6304 | pages = 82–4 | date = Jan 1991 | pmid = 1985270 | doi = 10.1038/349082a0 }}
* {{cite journal | vauthors = Brown CJ, Lafreniere RG, Powers VE, Sebastio G, Ballabio A, Pettigrew AL, Ledbetter DH, Levy E, Craig IW, Willard HF | title = Localization of the X inactivation centre on the human X chromosome in Xq13 | journal = Nature | volume = 349 | issue = 6304 | pages = 82–4 | date = January 1991 | pmid = 1985270 | doi = 10.1038/349082a0 }}
* {{cite journal | vauthors = Clemson CM, McNeil JA, Willard HF, Lawrence JB | title = XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure | journal = The Journal of Cell Biology | volume = 132 | issue = 3 | pages = 259–75 | date = Feb 1996 | pmid = 8636206 | pmc = 2120729 | doi = 10.1083/jcb.132.3.259 }}
* {{cite journal | vauthors = Clemson CM, McNeil JA, Willard HF, Lawrence JB | title = XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure | journal = The Journal of Cell Biology | volume = 132 | issue = 3 | pages = 259–75 | date = February 1996 | pmid = 8636206 | pmc = 2120729 | doi = 10.1083/jcb.132.3.259 }}
* {{cite journal | vauthors = Hendrich BD, Plenge RM, Willard HF | title = Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation | journal = Nucleic Acids Research | volume = 25 | issue = 13 | pages = 2661–71 | date = Jul 1997 | pmid = 9185579 | pmc = 146792 | doi = 10.1093/nar/25.13.2661 }}
* {{cite journal | vauthors = Hendrich BD, Plenge RM, Willard HF | title = Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation | journal = Nucleic Acids Research | volume = 25 | issue = 13 | pages = 2661–71 | date = July 1997 | pmid = 9185579 | pmc = 146792 | doi = 10.1093/nar/25.13.2661 }}
* {{cite journal | vauthors = Plenge RM, Hendrich BD, Schwartz C, Arena JF, Naumova A, Sapienza C, Winter RM, Willard HF | title = A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation | journal = Nature Genetics | volume = 17 | issue = 3 | pages = 353–6 | date = Nov 1997 | pmid = 9354806 | doi = 10.1038/ng1197-353 }}
* {{cite journal | vauthors = Plenge RM, Hendrich BD, Schwartz C, Arena JF, Naumova A, Sapienza C, Winter RM, Willard HF | title = A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation | journal = Nature Genetics | volume = 17 | issue = 3 | pages = 353–6 | date = November 1997 | pmid = 9354806 | doi = 10.1038/ng1197-353 }}
* {{cite journal | vauthors = Hong YK, Ontiveros SD, Strauss WM | title = A revision of the human XIST gene organization and structural comparison with mouse Xist | journal = Mammalian Genome | volume = 11 | issue = 3 | pages = 220–4 | date = Mar 2000 | pmid = 10723727 | doi = 10.1007/s003350010040 }}
* {{cite journal | vauthors = Hong YK, Ontiveros SD, Strauss WM | title = A revision of the human XIST gene organization and structural comparison with mouse Xist | journal = Mammalian Genome | volume = 11 | issue = 3 | pages = 220–4 | date = March 2000 | pmid = 10723727 | doi = 10.1007/s003350010040 }}
* {{cite journal | vauthors = Hall LL, Byron M, Sakai K, Carrel L, Willard HF, Lawrence JB | title = An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 99 | issue = 13 | pages = 8677–82 | date = Jun 2002 | pmid = 12072569 | pmc = 124357 | doi = 10.1073/pnas.132468999 }}
* {{cite journal | vauthors = Hall LL, Byron M, Sakai K, Carrel L, Willard HF, Lawrence JB | title = An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 99 | issue = 13 | pages = 8677–82 | date = June 2002 | pmid = 12072569 | pmc = 124357 | doi = 10.1073/pnas.132468999 }}
* {{cite journal | vauthors = Ganesan S, Silver DP, Greenberg RA, Avni D, Drapkin R, Miron A, Mok SC, Randrianarison V, Brodie S, Salstrom J, Rasmussen TP, Klimke A, Marrese C, Marahrens Y, Deng CX, Feunteun J, Livingston DM | title = BRCA1 supports XIST RNA concentration on the inactive X chromosome | journal = Cell | volume = 111 | issue = 3 | pages = 393–405 | date = Nov 2002 | pmid = 12419249 | doi = 10.1016/S0092-8674(02)01052-8 }}
* {{cite journal | vauthors = Ganesan S, Silver DP, Greenberg RA, Avni D, Drapkin R, Miron A, Mok SC, Randrianarison V, Brodie S, Salstrom J, Rasmussen TP, Klimke A, Marrese C, Marahrens Y, Deng CX, Feunteun J, Livingston DM | title = BRCA1 supports XIST RNA concentration on the inactive X chromosome | journal = Cell | volume = 111 | issue = 3 | pages = 393–405 | date = November 2002 | pmid = 12419249 | doi = 10.1016/S0092-8674(02)01052-8 }}
* {{cite journal | vauthors = Kawakami T, Okamoto K, Sugihara H, Hattori T, Reeve AE, Ogawa O, Okada Y | title = The roles of supernumerical X chromosomes and XIST expression in testicular germ cell tumors | journal = The Journal of Urology | volume = 169 | issue = 4 | pages = 1546–52 | date = Apr 2003 | pmid = 12629412 | doi = 10.1097/01.ju.0000044927.23323.5a }}
* {{cite journal | vauthors = Kawakami T, Okamoto K, Sugihara H, Hattori T, Reeve AE, Ogawa O, Okada Y | title = The roles of supernumerical X chromosomes and XIST expression in testicular germ cell tumors | journal = The Journal of Urology | volume = 169 | issue = 4 | pages = 1546–52 | date = April 2003 | pmid = 12629412 | doi = 10.1097/01.ju.0000044927.23323.5a }}
* {{cite journal | vauthors = Pugacheva EM, Tiwari VK, Abdullaev Z, Vostrov AA, Flanagan PT, Quitschke WW, Loukinov DI, Ohlsson R, Lobanenkov VV | title = Familial cases of point mutations in the XIST promoter reveal a correlation between CTCF binding and pre-emptive choices of X chromosome inactivation | journal = Human Molecular Genetics | volume = 14 | issue = 7 | pages = 953–65 | date = Apr 2005 | pmid = 15731119 | doi = 10.1093/hmg/ddi089 }}
* {{cite journal | vauthors = Pugacheva EM, Tiwari VK, Abdullaev Z, Vostrov AA, Flanagan PT, Quitschke WW, Loukinov DI, Ohlsson R, Lobanenkov VV | title = Familial cases of point mutations in the XIST promoter reveal a correlation between CTCF binding and pre-emptive choices of X chromosome inactivation | journal = Human Molecular Genetics | volume = 14 | issue = 7 | pages = 953–65 | date = April 2005 | pmid = 15731119 | doi = 10.1093/hmg/ddi089 }}
* {{cite journal | vauthors = Vasques LR, Stabellini R, Xue F, Tian XC, Soukoyan M, Pereira LV | title = XIST repression in the absence of DNMT1 and DNMT3B | journal = DNA Research | volume = 12 | issue = 5 | pages = 373–8 | year = 2007 | pmid = 16769694 | doi = 10.1093/dnares/dsi013 }}
* {{cite journal | vauthors = Vasques LR, Stabellini R, Xue F, Tian XC, Soukoyan M, Pereira LV | title = XIST repression in the absence of DNMT1 and DNMT3B | journal = DNA Research | volume = 12 | issue = 5 | pages = 373–8 | year = 2007 | pmid = 16769694 | doi = 10.1093/dnares/dsi013 }}
* {{cite journal | vauthors = Cohen HR, Panning B | title = XIST RNA exhibits nuclear retention and exhibits reduced association with the export factor TAP/NXF1 | journal = Chromosoma | volume = 116 | issue = 4 | pages = 373–83 | date = Aug 2007 | pmid = 17333237 | doi = 10.1007/s00412-007-0100-1 }}
* {{cite journal | vauthors = Cohen HR, Panning B | title = XIST RNA exhibits nuclear retention and exhibits reduced association with the export factor TAP/NXF1 | journal = Chromosoma | volume = 116 | issue = 4 | pages = 373–83 | date = August 2007 | pmid = 17333237 | doi = 10.1007/s00412-007-0100-1 }}
* {{cite journal | vauthors = Chow JC, Hall LL, Baldry SE, Thorogood NP, Lawrence JB, Brown CJ | title = Inducible XIST-dependent X-chromosome inactivation in human somatic cells is reversible | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 104 | issue = 24 | pages = 10104–9 | date = Jun 2007 | pmid = 17537922 | pmc = 1891207 | doi = 10.1073/pnas.0610946104 }}
* {{cite journal | vauthors = Chow JC, Hall LL, Baldry SE, Thorogood NP, Lawrence JB, Brown CJ | title = Inducible XIST-dependent X-chromosome inactivation in human somatic cells is reversible | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 104 | issue = 24 | pages = 10104–9 | date = June 2007 | pmid = 17537922 | pmc = 1891207 | doi = 10.1073/pnas.0610946104 }}
* {{cite journal | vauthors = Vincent-Salomon A, Ganem-Elbaz C, Manié E, Raynal V, Sastre-Garau X, Stoppa-Lyonnet D, Stern MH, Heard E | title = X inactive-specific transcript RNA coating and genetic instability of the X chromosome in BRCA1 breast tumors | journal = Cancer Research | volume = 67 | issue = 11 | pages = 5134–40 | date = Jun 2007 | pmid = 17545591 | doi = 10.1158/0008-5472.CAN-07-0465 }}
* {{cite journal | vauthors = Vincent-Salomon A, Ganem-Elbaz C, Manié E, Raynal V, Sastre-Garau X, Stoppa-Lyonnet D, Stern MH, Heard E | title = X inactive-specific transcript RNA coating and genetic instability of the X chromosome in BRCA1 breast tumors | journal = Cancer Research | volume = 67 | issue = 11 | pages = 5134–40 | date = June 2007 | pmid = 17545591 | doi = 10.1158/0008-5472.CAN-07-0465 }}
* {{cite journal | vauthors = Plath K, Mlynarczyk-Evans S, Nusinow DA, Panning B | title = Xist RNA and the mechanism of X chromosome inactivation | journal = Annual Review of Genetics | volume = 36 | issue =  | pages = 233–78 | year = 2002 | pmid = 12429693 | doi = 10.1146/annurev.genet.36.042902.092433 }}
* {{cite journal | vauthors = Plath K, Mlynarczyk-Evans S, Nusinow DA, Panning B | title = Xist RNA and the mechanism of X chromosome inactivation | journal = Annual Review of Genetics | volume = 36 | issue =  | pages = 233–78 | year = 2002 | pmid = 12429693 | doi = 10.1146/annurev.genet.36.042902.092433 }}
* {{cite journal | vauthors = Brockdorff N | title = X-chromosome inactivation: closing in on proteins that bind Xist RNA | journal = Trends in Genetics | volume = 18 | issue = 7 | pages = 352–8 | date = Jul 2002 | pmid = 12127775 | doi = 10.1016/S0168-9525(02)02717-8 }}
* {{cite journal | vauthors = Brockdorff N | title = X-chromosome inactivation: closing in on proteins that bind Xist RNA | journal = Trends in Genetics | volume = 18 | issue = 7 | pages = 352–8 | date = July 2002 | pmid = 12127775 | doi = 10.1016/S0168-9525(02)02717-8 }}
* {{cite journal | vauthors = Panning B, Dausman J, Jaenisch R | title = X chromosome inactivation is mediated by Xist RNA stabilization | journal = Cell | volume = 90 | issue = 5 | pages = 907–16 | date = Sep 1997 | pmid = 9298902 | doi = 10.1016/S0092-8674(00)80355-4 }}
* {{cite journal | vauthors = Panning B, Dausman J, Jaenisch R | title = X chromosome inactivation is mediated by Xist RNA stabilization | journal = Cell | volume = 90 | issue = 5 | pages = 907–16 | date = September 1997 | pmid = 9298902 | doi = 10.1016/S0092-8674(00)80355-4 }}
* {{cite journal | vauthors = Chaumeil J, Le Baccon P, Wutz A, Heard E | title = A novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silenced | journal = Genes & Development | volume = 20 | issue = 16 | pages = 2223–37 | date = Aug 2006 | pmid = 16912274 | pmc = 1553206 | doi = 10.1101/gad.380906 }}
* {{cite journal | vauthors = Chaumeil J, Le Baccon P, Wutz A, Heard E | title = A novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silenced | journal = Genes & Development | volume = 20 | issue = 16 | pages = 2223–37 | date = August 2006 | pmid = 16912274 | pmc = 1553206 | doi = 10.1101/gad.380906 }}
* {{cite journal | vauthors = Brockdorff N, Ashworth A, Kay GF, Cooper P, Smith S, McCabe VM, Norris DP, Penny GD, Patel D, Rastan S | title = Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome | journal = Nature | volume = 351 | issue = 6324 | pages = 329–31 | date = May 1991 | pmid = 2034279 | doi = 10.1038/351329a0 }}
* {{cite journal | vauthors = Brockdorff N, Ashworth A, Kay GF, Cooper P, Smith S, McCabe VM, Norris DP, Penny GD, Patel D, Rastan S | title = Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome | journal = Nature | volume = 351 | issue = 6324 | pages = 329–31 | date = May 1991 | pmid = 2034279 | doi = 10.1038/351329a0 }}
* {{cite journal | vauthors = Sado T, Brockdorff N | title = Advances in understanding chromosome silencing by the long non-coding RNA Xist | journal = Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences | volume = 368 | issue = 1609 | pages = 20110325 | date = Jan 2013 | pmid = 23166390 | doi = 10.1098/rstb.2011.0325 | pmc=3539355}}
* {{cite journal | vauthors = Sado T, Brockdorff N | title = Advances in understanding chromosome silencing by the long non-coding RNA Xist | journal = Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences | volume = 368 | issue = 1609 | pages = 20110325 | date = January 2013 | pmid = 23166390 | pmc = 3539355 | doi = 10.1098/rstb.2011.0325 }}
* {{cite journal | vauthors = Pennisi E | title = Long noncoding RNAs may alter chromosome's 3D structure | journal = Science | volume = 340 | issue = 6135 | pages = 910 | date = May 2013 | pmid = 23704542 | doi = 10.1126/science.340.6135.910-a }}
* {{cite journal | vauthors = Pennisi E | title = Long noncoding RNAs may alter chromosome's 3D structure | journal = Science | volume = 340 | issue = 6135 | pages = 910 | date = May 2013 | pmid = 23704542 | doi = 10.1126/science.340.6135.910-a }}
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Latest revision as of 16:07, 23 November 2018

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Xist (X-inactive specific transcript) is an RNA gene on the X chromosome of the placental mammals that acts as a major effector of the X inactivation process.[1] It is a component of the Xic – X-chromosome inactivation centre[2] – along with two other RNA genes (Jpx and Ftx) and two protein genes (Tsx and Cnbp2).[3] The Xist RNA, a large (17 kb in humans)[4] transcript, is expressed on the inactive chromosome and not on the active one. It is processed in a similar way to mRNAs, through splicing and polyadenylation. However, it remains untranslated. It has been suggested that this RNA gene evolved at least partly from a protein coding gene that became a pseudogene.[5] The inactive X chromosome is coated with this transcript, which is essential for the inactivation.[6] X chromosomes lacking Xist will not be inactivated, while duplication of the Xist gene on another chromosome causes inactivation of that chromosome.[7]

Function

X inactivation is an early developmental process in mammalian females that transcriptionally silences one of the pair of X chromosomes, thus providing dosage equivalence between males and females (see dosage compensation). The process is regulated by several factors, including a region of chromosome X called the X inactivation center (XIC). The XIST gene is expressed exclusively from the XIC of the inactive X chromosome. The transcript is spliced but apparently does not encode a protein. The transcript remains in the nucleus where it coats the inactive X chromosome. Alternatively spliced transcript variants have been identified, but their full length sequences have not been determined.[1]

The functional role of the Xist transcript was definitively demonstrated in mouse female ES cells using a novel antisense technology, called peptide nucleic acid (PNA) interference mapping. In the reported experiments, a single 19-bp antisense cell-permeating PNA targeted against a particular region of Xist RNA prevented the formation of Xi and inhibited cis-silencing of X-linked genes. The association of the Xi with macro-histone H2A is also disturbed by PNA interference mapping.[8]

X-inactivation process occurs in mice even in the absence of this gene via epigenetic regulation, but Xist is required to stabilize this silencing.[9]

Gene location

The human Xist RNA gene is located on the long (q) arm of the X chromosome. The Xist RNA gene consists of conserved repeats within its structure and is also largely localized in the nucleus.[4] The Xist RNA gene consists of an A region, which contains 8 repeats separated by U-rich spacers. The A region appears to contain two long stem-loop structures that each include four repeats.[10] An ortholog of the Xist RNA gene in humans has been identified in mice. This ortholog is a 15 kb Xist RNA gene that is also localized in the nucleus. However, the ortholog does not consist of conserved repeats.[11] The gene also consists of an Xist Inactivation Center (XIC), which plays a major role in X inactivation.[12]

Transcript organization

A region

File:RepA Model Xist.png
Structure model of the repeat A (repA) region of Xist based on in vivo biochemical structure probing and comparative sequence analysis. Repeats 1 to 8(1/2) are numbered and boxed - they are shown in red on the cartoon of repA in the upper left hand panel. Reactive nucleotides are colored red, where open and closed circles are medium and strongly reactive, respectively (reactivity suggests that a nucleotide is unpaired or loosely structured). Consistent and compensatory mutations (single and double point mutations that preserve pairing) are annotated in blue and purple, respectively. Base pairs that are 100% conserved in rodents are bold and black, while those conserved in rodents and mammals are in green. The data and model are taken from Fang R, Moss WN, Rutenberg-Schoenberg M, Simon MD (December 2015). "Probing Xist RNA Structure in Cells Using Targeted Structure-Seq". PLoS Genetics. 11 (12): e1005668. doi:10.1371/journal.pgen.1005668. PMC 4672913. PMID 26646615..

The Xist RNA contains a region of conservation called the repeat A (repA) region that contains up to nine repeated elements.[10] It was initially suggested that repA repeats could fold back on themselves to form local intra-repeat stem-loop structures. Later work using in vitro biochemical structure probing proposed several inter-repeat stem-loop structures.[4][10] A recent study using in vivo biochemical probing and comparative sequence analysis proposed a revision of the repA structure model that includes both intra-repeat and inter-repeat folding found in previous models as well as novel features (see Figure). In addition to its agreement with the in vivo data, this revised model is highly conserved in rodents and mammals (including humans) suggesting functional importance for repA structure. Although the exact function of the repA region is uncertain, it was shown that the entire region is needed for efficient binding to the Suz12 protein.[10]

C region

The Xist RNA directly binds to the inactive X-chromosome through a chromatin binding region of the RNA transcript. The Xist chromatin binding region was first elucidated in female mouse fibroblastic cells. The primary chromatin binding region was shown to localize to the C-repeat region. The chromatin-binding region was functionally mapped and evaluated by using an approach for studying noncoding RNA function in living cells called peptide nucleic acid (PNA) interference mapping. In the reported experiments, a single 19-bp antisense cell-permeating PNA targeted against a particular region of Xist RNA caused the disruption of the Xi. The association of the Xi with macro-histone H2A is also disturbed by PNA interference mapping.[8]

X Inactivation Centre (XIC)

The Xist RNA gene lies within the X-Inactivation Centre (XIC), which plays a major role in Xist expression and X inactivation.[13] The XIC is located on the q arm of the X chromosome (Xq13). XIC regulates Xist in cis X inactivation, where Tsix, an antisense of Xist, downregulates the expression of Xist. The Xist promoter of XIC is the master regulator of X inactivation.[12] X inactivation plays a key role in dosage compensation.

Tsix antisense transcript

The Tsix antisense gene is a transcript of the Xist gene at the XIC center.[14] The Tsix antisense transcript acts in cis to repress the transcription of Xist, which negatively regulates its expression. The mechanism behind how Tsix modulates Xist activity in cis is poorly understood; however, there are a few theories on its mechanism. One theory is that Tsix is involved in chromatin modification at the Xist locus and another is that transcription factors of pluripotent cells play a role in Xist repression.[15]

Regulation of the Xist promoter

Methylation

The Tsix antisense is believed to activate DNA methyl transferases that methylate the Xist promoter, in return resulting in inhibition of the Xist promoter and thus the expression of the Xist gene.[16] Methylation of histone 3 lysine 4 (H3K4) produces an active chromatin structure, which recruits transcription factors and thus allows for transcription to occur, therefore in this case the transcription of Xist.[17]

dsRNA and RNAi

A dsRNA and RNAi pathway have been also proposed to play a role in regulation of the Xist Promoter. Dicer is an RNAi enzyme and it is believed to cleave the duplex of Xist and Tsix at the beginning of X inactivation, to small ~30 nucleotide RNAs, which have been termed xiRNAs, These xiRNAs are believed to be involved in repressing Xist on the probable active X chromosome based upon studies. A study was conducted where normal endogenous Dicer levels were decreased to 5%, which led to an increase in Xist expression in undifferentiated cells, thus supporting the role of xiRNAs in Xist repression.[18] The role and mechanism of xiRNAs is still under examination and debate.[citation needed]

Tsix independent mechanisms

Pluripotent cell transcriptional factors

Pluripotent stem cells express transcription factors Nanog, Oct4 and Sox2 that seem to play a role in repressing Xist. In the absence of Tsix in pluripotent cells, Xist is repressed, where a mechanism has been proposed that these transcription factors cause splicing to occur at intron 1 at the binding site of these factors on the Xist gene, which inhibits Xist expression[15] A study was conducted where Nanog or Oct4 transcription factors were depleted in pluripotent cells, which resulted in the upregulation of Xist. From this study, it is proposed that Nanog and Oct4 are involved in the repression of Xist expression.[19]

Polycomb repressive complex

Polycomb repressive complex 2 (PRC2) consist of a class of polycomb group proteins that are involved in catalyzing the trimethylation of histone H3 on lysine 27 (K27), which results in chromatin repression, and thus leads to transcriptional silencing. Xist RNA recruits polycomb complexes to the inactive X chromosome at the onset of XCI.[20] SUZ12 is a component of the PRC2 and contains a zinc finger domain. The zinc finger domain is believed to bind to the RNA molecule.[21] The PRC2 has been observed to repress Xist expression independent of the Tsix antisense transcript, although the definite mechanism is still not known.

Dosage compensation

X inactivation plays a key role in dosage compensation mechanisms that allow for equal expression of the X and autosomal chromosomes.[22] Different species have different dosage compensation methods, with all of the methods involving the regulation of an X chromosome from one of the either sexes.[22] Some methods involved in dosage compensation to inactivate one of the X chromosomes from one of the sexes are Tsix antisense gene, DNA methylation and DNA acetylation;[23] however, the definite mechanism of X inactivation is still poorly understood. If one of the X chromosomes is not inactivated or is partially expressed, it could lead to over expression of the X chromosome and it could be lethal in some cases.

Turner's Syndrome is one example of where dosage compensation does not equally express the X chromosome, and in females one of the X chromosomes is missing or has abnormalities, which leads to physical abnormalities and also gonadal dysfunction in females due to the one missing or abnormal X chromosome. Turner's syndrome is also referred to as a monosomy X condition.[24]

X inactivation cycle

Xist expression and X inactivation change throughout embryonic development. In early embryogenesis, the oocyte and sperm do not express Xist and the X chromosome remains active. After fertilization, when the cells are in the 2 to 4 cell stage, Xist transcripts are expressed from parent X chromosome(Xp) in every cell, causing that X chromosome to become imprinted and inactivated. Some cells develop into pluripotent cells (the inner cell mass) when the blastocyte forms. There, the imprint is removed, leading to the downregulation of Xist and thus reactivation of the inactive X chromosome. Recent data suggests that Xist activity is regulated by an anti-sense transcript.[25] The epiblast cells are then formed and they begin to be differentiated, and the Xist is upregulated from either of the two X chromosomes and at random in ICM, but the Xist is maintained in epiblast, an X is inactivated and the Xist allele is turned off in the active X chromosome. In maturing XX primordial germ cells, Xist is downregulated and X reactivation occurs once again.[26]

Disease linkage

Mutations in the XIST promoter cause familial skewed X inactivation.[1]

Interactions

XIST (gene) has been shown to interact with BRCA1.[27][28]

See also

References

  1. ↑ 1.0 1.1 1.2 "Entrez Gene: XIST X (inactive)-specific transcript".
  2. ↑ Chow JC, Yen Z, Ziesche SM, Brown CJ (2005). "Silencing of the mammalian X chromosome". Annual Review of Genomics and Human Genetics. 6: 69–92. doi:10.1146/annurev.genom.6.080604.162350. PMID 16124854.
  3. ↑ Chureau C, Prissette M, Bourdet A, Barbe V, Cattolico L, Jones L, Eggen A, Avner P, Duret L (June 2002). "Comparative sequence analysis of the X-inactivation center region in mouse, human, and bovine". Genome Research. 12 (6): 894–908. doi:10.1101/gr.152902 (inactive 2018-09-05). PMC 1383731. PMID 12045143.
  4. ↑ 4.0 4.1 4.2 Brown CJ, Hendrich BD, Rupert JL, Lafrenière RG, Xing Y, Lawrence J, Willard HF (October 1992). "The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus". Cell. 71 (3): 527–42. doi:10.1016/0092-8674(92)90520-M. PMID 1423611.
  5. ↑ Duret L, Chureau C, Samain S, Weissenbach J, Avner P (June 2006). "The Xist RNA gene evolved in eutherians by pseudogenization of a protein-coding gene". Science. 312 (5780): 1653–5. doi:10.1126/science.1126316. PMID 16778056.
  6. ↑ Ng K, Pullirsch D, Leeb M, Wutz A (January 2007). "Xist and the order of silencing" (Review Article). EMBO Reports. 8 (1): 34–9. doi:10.1038/sj.embor.7400871. PMC 1796754. PMID 17203100. Figure 1 Xist RNA encompasses the X from which it is transcribed.
  7. ↑ Penny GD, Kay GF, Sheardown SA, Rastan S, Brockdorff N (1996). "Requirement for Xist in X chromosome inactivation". Nature. 379 (6561): 131–7. doi:10.1038/379131a0. PMID 8538762. closed access publication – behind paywall
  8. ↑ 8.0 8.1 Beletskii A, Hong YK, Pehrson J, Egholm M, Strauss WM (July 2001). "PNA interference mapping demonstrates functional domains in the noncoding RNA Xist". Proceedings of the National Academy of Sciences of the United States of America. 98 (16): 9215–20. doi:10.1073/pnas.161173098. PMC 55400. PMID 11481485.
  9. ↑ Kalantry S, Purushothaman S, Bowen RB, Starmer J, Magnuson T (July 2009). "Evidence of Xist RNA-independent initiation of mouse imprinted X-chromosome inactivation". Nature. 460 (7255): 647–51. doi:10.1038/nature08161. PMC 2754729. PMID 19571810.
  10. ↑ 10.0 10.1 10.2 10.3 Maenner S, Blaud M, Fouillen L, Savoye A, Marchand V, Dubois A, Sanglier-Cianférani S, Van Dorsselaer A, Clerc P, Avner P, Visvikis A, Branlant C (January 2010). Hall K, ed. "2-D structure of the A region of Xist RNA and its implication for PRC2 association". PLoS Biology. 8 (1): e1000276. doi:10.1371/journal.pbio.1000276. PMC 2796953. PMID 20052282.
  11. ↑ Brockdorff N, Ashworth A, Kay GF, McCabe VM, Norris DP, Cooper PJ, Swift S, Rastan S (1992). "The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus". Cell. 71 (3): 515–26. doi:10.1016/0092-8674(92)90519-I. PMID 1423610.
  12. ↑ 12.0 12.1 Lee JT, Davidow LS, Warshawsky D (April 1999). "Tsix, a gene antisense to Xist at the X-inactivation centre". Nature Genetics. 21 (4): 400–4. doi:10.1038/7734. PMID 10192391.
  13. ↑ Herzing LB, Romer JT, Horn JM, Ashworth A (March 1997). "Xist has properties of the X-chromosome inactivation centre". Nature. 386 (6622): 272–5. doi:10.1038/386272a0. PMID 9069284.
  14. ↑ Lee JT, Davidow LS, Warshawsky D (April 1999). "Tsix, a gene antisense to Xist at the X-inactivation centre". Nature Genetics. 21 (4): 400–4. doi:10.1038/7734. PMID 10192391.
  15. ↑ 15.0 15.1 Senner CE, Brockdorff N (April 2009). "Xist gene regulation at the onset of X inactivation". Current Opinion in Genetics & Development. 19 (2): 122–6. doi:10.1016/j.gde.2009.03.003. PMID 19345091.
  16. ↑ Nesterova TB, Popova BC, Cobb BS, Norton S, Senner CE, Tang YA, Spruce T, Rodriguez TA, Sado T, Merkenschlager M, Brockdorff N (October 2008). "Dicer regulates Xist promoter methylation in ES cells indirectly through transcriptional control of Dnmt3a". Epigenetics & Chromatin. 1 (1): 2. doi:10.1186/1756-8935-1-2. PMC 257704. PMID 19014663.
  17. ↑ Navarro P, Pichard S, Ciaudo C, Avner P, Rougeulle C (June 2005). "Tsix transcription across the Xist gene alters chromatin conformation without affecting Xist transcription: implications for X-chromosome inactivation". Genes & Development. 19 (12): 1474–84. doi:10.1101/gad.341105. PMC 1151664. PMID 15964997.
  18. ↑ Ogawa Y, Sun BK, Lee JT (June 2008). "Intersection of the RNA interference and X-inactivation pathways". Science. 320 (5881): 1336–41. doi:10.1126/science.1157676. PMC 2584363. PMID 18535243.
  19. ↑ Navarro P, Chambers I, Karwacki-Neisius V, Chureau C, Morey C, Rougeulle C, Avner P (September 2008). "Molecular coupling of Xist regulation and pluripotency". Science. 321 (5896): 1693–5. doi:10.1126/science.1160952. PMID 18802003.
  20. ↑ Zhao J, Sun BK, Erwin JA, Song JJ, Lee JT (October 2008). "Polycomb proteins targeted by a short repeat RNA to the mouse X chromosome". Science. 322 (5902): 750–6. doi:10.1126/science.1163045. PMC 2748911. PMID 18974356.
  21. ↑ de Napoles M, Mermoud JE, Wakao R, Tang YA, Endoh M, Appanah R, Nesterova TB, Silva J, Otte AP, Vidal M, Koseki H, Brockdorff N (2004). "Polycomb group proteins Ring1A/B link ubiquitylation of histone H2A to heritable gene silencing and X inactivation". Developmental Cell. 7 (5): 663–76. doi:10.1016/j.devcel.2004.10.005. PMID 15525528.
  22. ↑ 22.0 22.1 Nguyen DK, Disteche CM (January 2006). "Dosage compensation of the active X chromosome in mammals". Nature Genetics. 38 (1): 47–53. doi:10.1038/ng1705. PMID 16341221.
  23. ↑ Csankovszki G, Nagy A, Jaenisch R (May 2001). "Synergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivation". The Journal of Cell Biology. 153 (4): 773–84. doi:10.1083/jcb.153.4.773. PMC 2192370. PMID 11352938.
  24. ↑ Chenga MK, Nguyena KD, Disteche CM (2006). "Dosage compensation of the X chromosome and Turner syndrome=International-Congress-series". International Congress Series. 1298: 3–8. doi:10.1016/j.ics.2006.06.012.
  25. ↑ Mak W, Nesterova TB, de Napoles M, Appanah R, Yamanaka S, Otte AP, Brockdorff N (January 2004). "Reactivation of the paternal X chromosome in early mouse embryos". Science. 303 (5658): 666–9. doi:10.1126/science.1092674. PMID 14752160.
  26. ↑ Nesterova TB, Mermoud JE, Hilton K, Pehrson J, Surani MA, McLaren A, Brockdorff N (January 2002). "Xist expression and macroH2A1.2 localisation in mouse primordial and pluripotent embryonic germ cells". Differentiation; Research in Biological Diversity. 69 (4–5): 216–25. doi:10.1046/j.1432-0436.2002.690415.x. PMID 11841480.
  27. ↑ Ganesan S, Silver DP, Drapkin R, Greenberg R, Feunteun J, Livingston DM (January 2004). "Association of BRCA1 with the inactive X chromosome and XIST RNA". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 359 (1441): 123–8. doi:10.1098/rstb.2003.1371. PMC 1693294. PMID 15065664.
  28. ↑ Ganesan S, Silver DP, Greenberg RA, Avni D, Drapkin R, Miron A, Mok SC, Randrianarison V, Brodie S, Salstrom J, Rasmussen TP, Klimke A, Marrese C, Marahrens Y, Deng CX, Feunteun J, Livingston DM (November 2002). "BRCA1 supports XIST RNA concentration on the inactive X chromosome". Cell. 111 (3): 393–405. doi:10.1016/S0092-8674(02)01052-8. PMID 12419249.

Further reading

External links

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