Hepatocyte nuclear factor 4 alpha: Difference between revisions

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{{See also|MODY 1}}
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'''Hepatocyte nuclear factor 4 alpha''' ('''HNF4A''') also known as '''NR2A1''' (nuclear receptor subfamily 2, group A, member 1) is a [[nuclear receptor]] that in humans is encoded by the ''HNF4A'' gene.<ref name="pmid7926813">{{cite journal | vauthors = Chartier FL, Bossu JP, Laudet V, Fruchart JC, Laine B | title = Cloning and sequencing of cDNAs encoding the human hepatocyte nuclear factor 4 indicate the presence of two isoforms in human liver | journal = Gene | volume = 147 | issue = 2 | pages = 269–72 | date = Sep 1994 | pmid = 7926813 | doi = 10.1016/0378-1119(94)90079-5 }}</ref><ref name="pmid9048927">{{cite journal | vauthors = Argyrokastritis A, Kamakari S, Kapsetaki M, Kritis A, Talianidis I, Moschonas NK | title = Human hepatocyte nuclear factor-4 (hHNF-4) gene maps to 20q12-q13.1 between PLCG1 and D20S17 | journal = Human Genetics | volume = 99 | issue = 2 | pages = 233–6 | date = Feb 1997 | pmid = 9048927 | doi = 10.1007/s004390050345 }}</ref>
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
== Function ==
{{GNF_Protein_box
| image = PBB_Protein_HNF4A_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1m7w.
| PDB = {{PDB2|1m7w}}, {{PDB2|1pzl}}
| Name = Hepatocyte nuclear factor 4, alpha
| HGNCid = 5024
| Symbol = HNF4A
| AltSymbols =; FLJ39654; HNF4; HNF4a7; HNF4a8; HNF4a9; MODY; MODY1; NR2A1; NR2A21; TCF; TCF14
| OMIM = 600281
| ECnumber = 
| Homologene = 395
| MGIid = 109128
| GeneAtlas_image1 = PBB_GE_HNF4A_216889_s_at_tn.png
| GeneAtlas_image2 = PBB_GE_HNF4A_208429_x_at_tn.png
| GeneAtlas_image3 = PBB_GE_HNF4A_214832_at_tn.png
| Function = {{GNF_GO|id=GO:0003700 |text = transcription factor activity}} {{GNF_GO|id=GO:0003702 |text = RNA polymerase II transcription factor activity}} {{GNF_GO|id=GO:0003707 |text = steroid hormone receptor activity}} {{GNF_GO|id=GO:0005496 |text = steroid binding}} {{GNF_GO|id=GO:0008270 |text = zinc ion binding}} {{GNF_GO|id=GO:0016439 |text = tRNA-pseudouridine synthase activity}} {{GNF_GO|id=GO:0043565 |text = sequence-specific DNA binding}} {{GNF_GO|id=GO:0046872 |text = metal ion binding}}
| Component = {{GNF_GO|id=GO:0005634 |text = nucleus}}
| Process = {{GNF_GO|id=GO:0006350 |text = transcription}} {{GNF_GO|id=GO:0006355 |text = regulation of transcription, DNA-dependent}} {{GNF_GO|id=GO:0006357 |text = regulation of transcription from RNA polymerase II promoter}} {{GNF_GO|id=GO:0006629 |text = lipid metabolic process}} {{GNF_GO|id=GO:0007596 |text = blood coagulation}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 3172
    | Hs_Ensembl = ENSG00000101076
    | Hs_RefseqProtein = NP_000448
    | Hs_RefseqmRNA = NM_000457
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 20
    | Hs_GenLoc_start = 42463324
    | Hs_GenLoc_end = 42493444
    | Hs_Uniprot = P41235
    | Mm_EntrezGene = 15378
    | Mm_Ensembl = ENSMUSG00000017950
    | Mm_RefseqmRNA = NM_008261
    | Mm_RefseqProtein = NP_032287
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 2
    | Mm_GenLoc_start = 163198277
    | Mm_GenLoc_end = 163264348
    | Mm_Uniprot = Q3UNX3
  }}
}}
'''Hepatocyte nuclear factor 4 alpha''' ('''HNF4A''') also known as '''NR2A1''' (nuclear receptor subfamily 2, group A, member 1) is a [[nuclear receptor]] encoded by the {{gene|HNF4A}} gene.


<!-- The PBB_Summary template is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
HNF-4α is a nuclear [[transcription factor]] that binds DNA as a homodimer. The encoded protein controls the expression of several genes, including [[HNF1A|hepatocyte nuclear factor 1 alpha]], a transcription factor which regulates the expression of several hepatic genes. This gene plays a role in development of the {{SWL|target=liver|type=involved_in_development_of}}, {{SWL|target=kidney|type=involved_in_development_of}}, and {{SWL|target=intestines|type=involved_in_development_of}}. Alternative splicing of this gene results in multiple transcript variants.<ref name="entrez">{{cite web | title = Entrez Gene: HNF4A hepatocyte nuclear factor 4, alpha| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3172| accessdate = }}</ref>
{{PBB_Summary
| section_title =
| summary_text = The protein encoded by this gene is a nuclear [[transcription factor]] which binds DNA as a homodimer. The encoded protein controls the expression of several genes, including hepatocyte nuclear factor 1 alpha, a transcription factor which regulates the expression of several hepatic genes. This gene may play a role in development of the liver, kidney, and intestines. Mutations in this gene have been associated with monogenic autosomal dominant non-insulin-dependent [[diabetes mellitus]] type I. Alternative splicing of this gene results in multiple transcript variants.<ref name="entrez">{{cite web | title = Entrez Gene: HNF4A hepatocyte nuclear factor 4, alpha| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3172| accessdate = }}</ref>
}}


==See also==
HNF4A is required for the [[pregnane X receptor|PXR]] and [[constitutive androstane receptor|CAR]]-mediated transcriptional activation of [[CYP3A4]].<ref name="pmid12514743">{{cite journal | vauthors = Tirona RG, Lee W, Leake BF, Lan LB, Cline CB, Lamba V, Parviz F, Duncan SA, Inoue Y, Gonzalez FJ, Schuetz EG, Kim RB | title = The orphan nuclear receptor HNF4alpha determines PXR- and CAR-mediated xenobiotic induction of CYP3A4 | journal = Nature Medicine | volume = 9 | issue = 2 | pages = 220–4 | date = Feb 2003 | pmid = 12514743 | doi = 10.1038/nm815 }}</ref> Genetic mutations in the ''HNF4A'' gene can influence the activity of HNF4α's downstream proteins such as CYP2D6, ''in vitro'' and ''in vivo''.<ref name="pmid18666237">{{cite journal | vauthors = Lee SS, Cha EY, Jung HJ, Shon JH, Kim EY, Yeo CW, Shin JG | title = Genetic polymorphism of hepatocyte nuclear factor-4alpha influences human cytochrome P450 2D6 activity | journal = Hepatology | volume = 48 | issue = 2 | pages = 635–45 | year = 2008 | pmid = 18666237 | doi = 10.1002/hep.22396 }}</ref><ref name="pmid23292115">{{cite journal | vauthors = Jiang F, Yeo CW, Lee SS, Oh MK, Ghim JL, Shon JH, Kim HS, Kim EY, Kim DH, Shin JG | title = Effect of HNF4α genetic polymorphism G60D on the pharmacokinetics of CYP2D6 substrate tolterodine in healthy Korean individuals | journal = Pharmacogenetics and Genomics | volume = 23 | issue = 3 | pages = 175–9 | year = 2013 | pmid = 23292115 | doi = 10.1097/FPC.0b013e32835de25e }}</ref>
 
The alkaloid [[berberine]] upregulates the expression of HNF4A.<ref name="pmid18932278">{{cite journal | vauthors = Wang ZQ, Lu FE, Leng SH, Fang XS, Chen G, Wang ZS, Dong LP, Yan ZQ | title = Facilitating effects of berberine on rat pancreatic islets through modulating hepatic nuclear factor 4 alpha expression and glucokinase activity | journal = World Journal of Gastroenterology | volume = 14 | issue = 39 | pages = 6004–11 | date = Oct 2008 | pmid = 18932278 | pmc = 2760199 | doi = 10.3748/wjg.14.6004 }}</ref>
 
This gene also plays a pivotal role in the expression and synthesis of [[SHBG]], an important [[glycoprotein]] made primarily in the [[liver]], which in addition to lowering insulin-resistance also serves in reducing levels of free [[Estrogen]] as-well as prolonging the half-life of [[Testosterone]].{{citation needed|date=March 2016}}
 
Function of HNF4A gene can be effectively examined by siRNA knockdown based on an independent validation.<ref>{{Cite journal|last=Munkácsy|first=Gyöngyi|last2=Sztupinszki|first2=Zsófia|last3=Herman|first3=Péter|last4=Bán|first4=Bence|last5=Pénzváltó|first5=Zsófia|last6=Szarvas|first6=Nóra|last7=Győrffy|first7=Balázs|date=2016-01-01|title=Validation of RNAi Silencing Efficiency Using Gene Array Data shows 18.5% Failure Rate across 429 Independent Experiments|url=http://linkinghub.elsevier.com/retrieve/pii/S2162253117300859|journal=Molecular Therapy - Nucleic Acids|language=English|volume=5|doi=10.1038/mtna.2016.66|issn=2162-2531|pmc=5056990|pmid=27673562}}</ref>
 
== Clinical significance ==
 
Mutations in the HNF4A gene are associated with a form of diabetes called [[maturity onset diabetes of the young]] (MODY).<ref name="pmid24559927">{{cite journal | vauthors = Yamagata K | title = Roles of HNF1α and HNF4α in pancreatic β-cells: lessons from a monogenic form of diabetes (MODY) | journal = Vitamins and Hormones | volume = 95 | issue = | pages = 407–23 | year = 2014 | pmid = 24559927 | doi = 10.1016/B978-0-12-800174-5.00016-8 }}</ref>
 
Increased amplification of hepatocyte nuclear factor 4 alpha has been observed in [[colorectal cancer]].<ref name="pmid25043054">{{cite journal | vauthors = Zhang B, Wang J, Wang X, Zhu J, Liu Q, Shi Z, Chambers MC, Zimmerman LJ, Shaddox KF, Kim S, Davies SR, Wang S, Wang P, Kinsinger CR, Rivers RC, Rodriguez H, Townsend RR, Ellis MJ, Carr SA, Tabb DL, Coffey RJ, Slebos RJ, Liebler DC | display-authors = 6 | title = Proteogenomic characterization of human colon and rectal cancer | journal = Nature | volume = 513 | issue = 7518 | pages = 382–7 | year = 2014 | pmid = 25043054 | pmc = 4249766 | doi = 10.1038/nature13438 | url = }}</ref>
 
== Interactions ==
 
Hepatocyte nuclear factor 4 alpha has been shown to [[Protein-protein interaction|interact]] with:
* [[Beta-catenin]],<ref name="pmid12944908">{{cite journal | vauthors = Mulholland DJ, Read JT, Rennie PS, Cox ME, Nelson CC | title = Functional localization and competition between the androgen receptor and T-cell factor for nuclear beta-catenin: a means for inhibition of the Tcf signaling axis | journal = Oncogene | volume = 22 | issue = 36 | pages = 5602–13 | date = Aug 2003 | pmid = 12944908 | doi = 10.1038/sj.onc.1206802 }}</ref>
* [[CREB binding protein]],<ref name="pmid9434765">{{cite journal | vauthors = Yoshida E, Aratani S, Itou H, Miyagishi M, Takiguchi M, Osumu T, Murakami K, Fukamizu A | title = Functional association between CBP and HNF4 in trans-activation | journal = Biochemical and Biophysical Research Communications | volume = 241 | issue = 3 | pages = 664–9 | date = Dec 1997 | pmid = 9434765 | doi = 10.1006/bbrc.1997.7871 }}</ref><ref name="pmid10085149">{{cite journal | vauthors = Dell H, Hadzopoulou-Cladaras M | title = CREB-binding protein is a transcriptional coactivator for hepatocyte nuclear factor-4 and enhances apolipoprotein gene expression | journal = The Journal of Biological Chemistry | volume = 274 | issue = 13 | pages = 9013–21 | date = Mar 1999 | pmid = 10085149 | doi = 10.1074/jbc.274.13.9013 }}</ref>
*  [[MED1]],<ref name=pmid12089346/><ref name=pmid12101254/>
* [[MED14]],<ref name="pmid12089346">{{cite journal | vauthors = Maeda Y, Rachez C, Hawel L, Byus CV, Freedman LP, Sladek FM | title = Polyamines modulate the interaction between nuclear receptors and vitamin D receptor-interacting protein 205 | journal = Molecular Endocrinology | volume = 16 | issue = 7 | pages = 1502–10 | date = Jul 2002 | pmid = 12089346 | doi = 10.1210/mend.16.7.0883 }}</ref><ref name="pmid12101254">{{cite journal | vauthors = Malik S, Wallberg AE, Kang YK, Roeder RG | title = TRAP/SMCC/mediator-dependent transcriptional activation from DNA and chromatin templates by orphan nuclear receptor hepatocyte nuclear factor 4 | journal = Molecular and Cellular Biology | volume = 22 | issue = 15 | pages = 5626–37 | date = Aug 2002 | pmid = 12101254 | pmc = 133960 | doi = 10.1128/MCB.22.15.5626-5637.2002 }}</ref>
* [[Small heterodimer partner]]<ref name="pmid10594021">{{cite journal | vauthors = Lee YK, Dell H, Dowhan DH, Hadzopoulou-Cladaras M, Moore DD | title = The orphan nuclear receptor SHP inhibits hepatocyte nuclear factor 4 and retinoid X receptor transactivation: two mechanisms for repression | journal = Molecular and Cellular Biology | volume = 20 | issue = 1 | pages = 187–95 | date = Jan 2000 | pmid = 10594021 | pmc = 85074 | doi = 10.1128/MCB.20.1.187-195.2000 }}</ref>
* [[Testicular receptor 4]],<ref name="pmid12522137">{{cite journal | vauthors = Lin WJ, Li J, Lee YF, Yeh SD, Altuwaijri S, Ou JH, Chang C | title = Suppression of hepatitis B virus core promoter by the nuclear orphan receptor TR4 | journal = The Journal of Biological Chemistry | volume = 278 | issue = 11 | pages = 9353–60 | date = Mar 2003 | pmid = 12522137 | doi = 10.1074/jbc.M205944200 }}</ref>
 
== See also ==
*[[Hepatocyte nuclear factor 4]]
*[[Hepatocyte nuclear factor 4]]
*[[Hepatocyte nuclear factors]]
*[[Hepatocyte nuclear factors]]


==References==
== References ==
{{reflist|2}}
{{Reflist|2}}


==Further reading==
== Further reading ==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading
* {{cite journal | vauthors = Winter WE, Nakamura M, House DV | title = Monogenic diabetes mellitus in youth. The MODY syndromes | journal = Endocrinology and Metabolism Clinics of North America | volume = 28 | issue = 4 | pages = 765–85 | date = Dec 1999 | pmid = 10609119 | doi = 10.1016/S0889-8529(05)70101-8 }}
| citations =
* {{cite journal | vauthors = Zannis VI, Kan HY, Kritis A, Zanni E, Kardassis D | title = Transcriptional regulation of the human apolipoprotein genes | journal = Frontiers in Bioscience | volume = 6 | issue =  | pages = D456-504 | date = Mar 2001 | pmid = 11229886 | doi = 10.2741/Zannis }}
*{{cite journal | author=Winter WE, Nakamura M, House DV |title=Monogenic diabetes mellitus in youth. The MODY syndromes. |journal=Endocrinol. Metab. Clin. North Am. |volume=28 |issue= 4 |pages= 765-85 |year= 2000 |pmid= 10609119 |doi= }}
* {{cite journal | vauthors = Gupta RK, Kaestner KH | title = HNF-4alpha: from MODY to late-onset type 2 diabetes | journal = Trends in Molecular Medicine | volume = 10 | issue = 11 | pages = 521–4 | date = Nov 2004 | pmid = 15519277 | doi = 10.1016/j.molmed.2004.09.004 }}
*{{cite journal | author=Zannis VI, Kan HY, Kritis A, ''et al.'' |title=Transcriptional regulation of the human apolipoprotein genes. |journal=Front. Biosci. |volume=6 |issue=  |pages= D456-504 |year= 2001 |pmid= 11229886 |doi= }}
* {{cite journal | vauthors = Mohlke KL, Boehnke M | title = The role of HNF4A variants in the risk of type 2 diabetes | journal = Current Diabetes Reports | volume = 5 | issue = 2 | pages = 149–56 | date = Apr 2005 | pmid = 15794920 | doi = 10.1007/s11892-005-0043-y }}
*{{cite journal | author=Gupta RK, Kaestner KH |title=HNF-4alpha: from MODY to late-onset type 2 diabetes. |journal=Trends in molecular medicine |volume=10 |issue= 11 |pages= 521-4 |year= 2005 |pmid= 15519277 |doi= 10.1016/j.molmed.2004.09.004 }}
* {{cite journal | vauthors = Love-Gregory L, Permutt MA | title = HNF4A genetic variants: role in diabetes | journal = Current Opinion in Clinical Nutrition and Metabolic Care | volume = 10 | issue = 4 | pages = 397–402 | date = Jul 2007 | pmid = 17563455 | doi = 10.1097/MCO.0b013e3281e3888d }}
*{{cite journal | author=Mohlke KL, Boehnke M |title=The role of HNF4A variants in the risk of type 2 diabetes. |journal=Curr. Diab. Rep. |volume=5 |issue= 2 |pages= 149-56 |year= 2005 |pmid= 15794920 |doi= }}
* {{cite journal | vauthors = Bell GI, Xiang KS, Newman MV, Wu SH, Wright LG, Fajans SS, Spielman RS, Cox NJ | title = Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 88 | issue = 4 | pages = 1484–8 | date = Feb 1991 | pmid = 1899928 | pmc = 51043 | doi = 10.1073/pnas.88.4.1484 }}
*{{cite journal | author=Love-Gregory L, Permutt MA |title=HNF4A genetic variants: role in diabetes. |journal=Current opinion in clinical nutrition and metabolic care |volume=10 |issue= 4 |pages= 397-402 |year= 2007 |pmid= 17563455 |doi= 10.1097/MCO.0b013e3281e3888d }}
* {{cite journal | vauthors = Ktistaki E, Ktistakis NT, Papadogeorgaki E, Talianidis I | title = Recruitment of hepatocyte nuclear factor 4 into specific intranuclear compartments depends on tyrosine phosphorylation that affects its DNA-binding and transactivation potential | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 92 | issue = 21 | pages = 9876–80 | date = Oct 1995 | pmid = 7568236 | pmc = 40905 | doi = 10.1073/pnas.92.21.9876 }}
*{{cite journal | author=Bell GI, Xiang KS, Newman MV, ''et al.'' |title=Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=88 |issue= 4 |pages= 1484-8 |year= 1991 |pmid= 1899928 |doi= }}
* {{cite journal | vauthors = Ginsburg GS, Ozer J, Karathanasis SK | title = Intestinal apolipoprotein AI gene transcription is regulated by multiple distinct DNA elements and is synergistically activated by the orphan nuclear receptor, hepatocyte nuclear factor 4 | journal = The Journal of Clinical Investigation | volume = 96 | issue = 1 | pages = 528–38 | date = Jul 1995 | pmid = 7615825 | pmc = 185227 | doi = 10.1172/JCI118065 }}
*{{cite journal | author=Ktistaki E, Ktistakis NT, Papadogeorgaki E, Talianidis I |title=Recruitment of hepatocyte nuclear factor 4 into specific intranuclear compartments depends on tyrosine phosphorylation that affects its DNA-binding and transactivation potential. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=92 |issue= 21 |pages= 9876-80 |year= 1995 |pmid= 7568236 |doi= }}
* {{cite journal | vauthors = Jiang G, Nepomuceno L, Hopkins K, Sladek FM | title = Exclusive homodimerization of the orphan receptor hepatocyte nuclear factor 4 defines a new subclass of nuclear receptors | journal = Molecular and Cellular Biology | volume = 15 | issue = 9 | pages = 5131–43 | date = Sep 1995 | pmid = 7651430 | pmc = 230760 | doi =  10.1128/mcb.15.9.5131}}
*{{cite journal | author=Ginsburg GS, Ozer J, Karathanasis SK |title=Intestinal apolipoprotein AI gene transcription is regulated by multiple distinct DNA elements and is synergistically activated by the orphan nuclear receptor, hepatocyte nuclear factor 4. |journal=J. Clin. Invest. |volume=96 |issue= 1 |pages= 528-38 |year= 1995 |pmid= 7615825 |doi= }}
* {{cite journal | vauthors = Chartier FL, Bossu JP, Laudet V, Fruchart JC, Laine B | title = Cloning and sequencing of cDNAs encoding the human hepatocyte nuclear factor 4 indicate the presence of two isoforms in human liver | journal = Gene | volume = 147 | issue = 2 | pages = 269–72 | date = Sep 1994 | pmid = 7926813 | doi = 10.1016/0378-1119(94)90079-5 }}
*{{cite journal | author=Jiang G, Nepomuceno L, Hopkins K, Sladek FM |title=Exclusive homodimerization of the orphan receptor hepatocyte nuclear factor 4 defines a new subclass of nuclear receptors. |journal=Mol. Cell. Biol. |volume=15 |issue= 9 |pages= 5131-43 |year= 1995 |pmid= 7651430 |doi=  }}
* {{cite journal | vauthors = Drewes T, Senkel S, Holewa B, Ryffel GU | title = Human hepatocyte nuclear factor 4 isoforms are encoded by distinct and differentially expressed genes | journal = Molecular and Cellular Biology | volume = 16 | issue = 3 | pages = 925–31 | date = Mar 1996 | pmid = 8622695 | pmc = 231074 | doi =  10.1128/mcb.16.3.925}}
*{{cite journal | author=Chartier FL, Bossu JP, Laudet V, ''et al.'' |title=Cloning and sequencing of cDNAs encoding the human hepatocyte nuclear factor 4 indicate the presence of two isoforms in human liver. |journal=Gene |volume=147 |issue= 2 |pages= 269-72 |year= 1994 |pmid= 7926813 |doi= }}
* {{cite journal | vauthors = Yamagata K, Furuta H, Oda N, Kaisaki PJ, Menzel S, Cox NJ, Fajans SS, Signorini S, Stoffel M, Bell GI | title = Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1) | journal = Nature | volume = 384 | issue = 6608 | pages = 458–60 | date = Dec 1996 | pmid = 8945471 | doi = 10.1038/384458a0 }}
*{{cite journal | author=Drewes T, Senkel S, Holewa B, Ryffel GU |title=Human hepatocyte nuclear factor 4 isoforms are encoded by distinct and differentially expressed genes. |journal=Mol. Cell. Biol. |volume=16 |issue= 3 |pages= 925-31 |year= 1996 |pmid= 8622695 |doi=  }}
* {{cite journal | vauthors = Kritis AA, Argyrokastritis A, Moschonas NK, Power S, Katrakili N, Zannis VI, Cereghini S, Talianidis I | title = Isolation and characterization of a third isoform of human hepatocyte nuclear factor 4 | journal = Gene | volume = 173 | issue = 2 | pages = 275–80 | date = Sep 1996 | pmid = 8964514 | doi = 10.1016/0378-1119(96)00183-7 }}
*{{cite journal | author=Yamagata K, Furuta H, Oda N, ''et al.'' |title=Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1) |journal=Nature |volume=384 |issue= 6608 |pages= 458-60 |year= 1997 |pmid= 8945471 |doi= 10.1038/384458a0 }}
* {{cite journal | vauthors = Argyrokastritis A, Kamakari S, Kapsetaki M, Kritis A, Talianidis I, Moschonas NK | title = Human hepatocyte nuclear factor-4 (hHNF-4) gene maps to 20q12-q13.1 between PLCG1 and D20S17 | journal = Human Genetics | volume = 99 | issue = 2 | pages = 233–6 | date = Feb 1997 | pmid = 9048927 | doi = 10.1007/s004390050345 }}
*{{cite journal | author=Kritis AA, Argyrokastritis A, Moschonas NK, ''et al.'' |title=Isolation and characterization of a third isoform of human hepatocyte nuclear factor 4. |journal=Gene |volume=173 |issue= 2 |pages= 275-80 |year= 1996 |pmid= 8964514 |doi= }}
* {{cite journal | vauthors = Thénot S, Henriquet C, Rochefort H, Cavaillès V | title = Differential interaction of nuclear receptors with the putative human transcriptional coactivator hTIF1 | journal = The Journal of Biological Chemistry | volume = 272 | issue = 18 | pages = 12062–8 | date = May 1997 | pmid = 9115274 | doi = 10.1074/jbc.272.18.12062 }}
*{{cite journal | author=Argyrokastritis A, Kamakari S, Kapsetaki M, ''et al.'' |title=Human hepatocyte nuclear factor-4 (hHNF-4) gene maps to 20q12-q13.1 between PLCG1 and D20S17. |journal=Hum. Genet. |volume=99 |issue= 2 |pages= 233-6 |year= 1997 |pmid= 9048927 |doi= }}
* {{cite journal | vauthors = Bulman MP, Dronsfield MJ, Frayling T, Appleton M, Bain SC, Ellard S, Hattersley AT | title = A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturity-onset diabetes of the young | journal = Diabetologia | volume = 40 | issue = 7 | pages = 859–62 | date = Jul 1997 | pmid = 9243109 | doi = 10.1007/s001250050760 }}
*{{cite journal | author=Thénot S, Henriquet C, Rochefort H, Cavaillès V |title=Differential interaction of nuclear receptors with the putative human transcriptional coactivator hTIF1. |journal=J. Biol. Chem. |volume=272 |issue= 18 |pages= 12062-8 |year= 1997 |pmid= 9115274 |doi= }}
* {{cite journal | vauthors = Møller AM, Urhammer SA, Dalgaard LT, Reneland R, Berglund L, Hansen T, Clausen JO, Lithell H, Pedersen O | title = Studies of the genetic variability of the coding region of the hepatocyte nuclear factor-4alpha in Caucasians with maturity onset NIDDM | journal = Diabetologia | volume = 40 | issue = 8 | pages = 980–3 | date = Aug 1997 | pmid = 9267996 | doi = 10.1007/s001250050778 }}
*{{cite journal | author=Bulman MP, Dronsfield MJ, Frayling T, ''et al.'' |title=A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturity-onset diabetes of the young. |journal=Diabetologia |volume=40 |issue= 7 |pages= 859-62 |year= 1997 |pmid= 9243109 |doi= }}
* {{cite journal | vauthors = Lindner T, Gragnoli C, Furuta H, Cockburn BN, Petzold C, Rietzsch H, Weiss U, Schulze J, Bell GI | title = Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4alpha/MODY1 gene | journal = The Journal of Clinical Investigation | volume = 100 | issue = 6 | pages = 1400–5 | date = Sep 1997 | pmid = 9294105 | pmc = 508318 | doi = 10.1172/JCI119660 }}
*{{cite journal | author=Møller AM, Urhammer SA, Dalgaard LT, ''et al.'' |title=Studies of the genetic variability of the coding region of the hepatocyte nuclear factor-4alpha in Caucasians with maturity onset NIDDM. |journal=Diabetologia |volume=40 |issue= 8 |pages= 980-3 |year= 1998 |pmid= 9267996 |doi= }}
* {{cite journal | vauthors = Furuta H, Iwasaki N, Oda N, Hinokio Y, Horikawa Y, Yamagata K, Yano N, Sugahiro J, Ogata M, Ohgawara H, Omori Y, Iwamoto Y, Bell GI | title = Organization and partial sequence of the hepatocyte nuclear factor-4 alpha/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY | journal = Diabetes | volume = 46 | issue = 10 | pages = 1652–7 | date = Oct 1997 | pmid = 9313765 | doi = 10.2337/diabetes.46.10.1652 }}
*{{cite journal | author=Lindner T, Gragnoli C, Furuta H, ''et al.'' |title=Hepatic function in a family with a nonsense mutation (R154X) in the hepatocyte nuclear factor-4alpha/MODY1 gene. |journal=J. Clin. Invest. |volume=100 |issue= 6 |pages= 1400-5 |year= 1997 |pmid= 9294105 |doi= }}
* {{cite journal | vauthors = Stoffel M, Duncan SA | title = The maturity-onset diabetes of the young (MODY1) transcription factor HNF4alpha regulates expression of genes required for glucose transport and metabolism | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 94 | issue = 24 | pages = 13209–14 | date = Nov 1997 | pmid = 9371825 | pmc = 24288 | doi = 10.1073/pnas.94.24.13209 }}
*{{cite journal | author=Furuta H, Iwasaki N, Oda N, ''et al.'' |title=Organization and partial sequence of the hepatocyte nuclear factor-4 alpha/MODY1 gene and identification of a missense mutation, R127W, in a Japanese family with MODY. |journal=Diabetes |volume=46 |issue= 10 |pages= 1652-7 |year= 1997 |pmid= 9313765 |doi= }}
*{{cite journal | author=Stoffel M, Duncan SA |title=The maturity-onset diabetes of the young (MODY1) transcription factor HNF4alpha regulates expression of genes required for glucose transport and metabolism. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=94 |issue= 24 |pages= 13209-14 |year= 1998 |pmid= 9371825 |doi= }}
}}
{{refend}}
{{refend}}
== External links ==
* {{FactorBook|HNF4A}}


{{NLM content}}
{{NLM content}}
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{{PDB Gallery|geneid=3172}}
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[[Category:Intracellular receptors]]
[[Category:Intracellular receptors]]
[[Category:Transcription factors]]
[[Category:Transcription factors]]
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Latest revision as of 16:11, 31 August 2017

See also: MODY 1
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Identifiers
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Orthologs
SpeciesHumanMouse
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Hepatocyte nuclear factor 4 alpha (HNF4A) also known as NR2A1 (nuclear receptor subfamily 2, group A, member 1) is a nuclear receptor that in humans is encoded by the HNF4A gene.[1][2]

Function

HNF-4α is a nuclear transcription factor that binds DNA as a homodimer. The encoded protein controls the expression of several genes, including hepatocyte nuclear factor 1 alpha, a transcription factor which regulates the expression of several hepatic genes. This gene plays a role in development of the liver , kidney , and intestines . Alternative splicing of this gene results in multiple transcript variants.[3]

HNF4A is required for the PXR and CAR-mediated transcriptional activation of CYP3A4.[4] Genetic mutations in the HNF4A gene can influence the activity of HNF4α's downstream proteins such as CYP2D6, in vitro and in vivo.[5][6]

The alkaloid berberine upregulates the expression of HNF4A.[7]

This gene also plays a pivotal role in the expression and synthesis of SHBG, an important glycoprotein made primarily in the liver, which in addition to lowering insulin-resistance also serves in reducing levels of free Estrogen as-well as prolonging the half-life of Testosterone.[citation needed]

Function of HNF4A gene can be effectively examined by siRNA knockdown based on an independent validation.[8]

Clinical significance

Mutations in the HNF4A gene are associated with a form of diabetes called maturity onset diabetes of the young (MODY).[9]

Increased amplification of hepatocyte nuclear factor 4 alpha has been observed in colorectal cancer.[10]

Interactions

Hepatocyte nuclear factor 4 alpha has been shown to interact with:

See also

References

  1. ↑ Chartier FL, Bossu JP, Laudet V, Fruchart JC, Laine B (Sep 1994). "Cloning and sequencing of cDNAs encoding the human hepatocyte nuclear factor 4 indicate the presence of two isoforms in human liver". Gene. 147 (2): 269–72. doi:10.1016/0378-1119(94)90079-5. PMID 7926813.
  2. ↑ Argyrokastritis A, Kamakari S, Kapsetaki M, Kritis A, Talianidis I, Moschonas NK (Feb 1997). "Human hepatocyte nuclear factor-4 (hHNF-4) gene maps to 20q12-q13.1 between PLCG1 and D20S17". Human Genetics. 99 (2): 233–6. doi:10.1007/s004390050345. PMID 9048927.
  3. ↑ "Entrez Gene: HNF4A hepatocyte nuclear factor 4, alpha".
  4. ↑ Tirona RG, Lee W, Leake BF, Lan LB, Cline CB, Lamba V, Parviz F, Duncan SA, Inoue Y, Gonzalez FJ, Schuetz EG, Kim RB (Feb 2003). "The orphan nuclear receptor HNF4alpha determines PXR- and CAR-mediated xenobiotic induction of CYP3A4". Nature Medicine. 9 (2): 220–4. doi:10.1038/nm815. PMID 12514743.
  5. ↑ Lee SS, Cha EY, Jung HJ, Shon JH, Kim EY, Yeo CW, Shin JG (2008). "Genetic polymorphism of hepatocyte nuclear factor-4alpha influences human cytochrome P450 2D6 activity". Hepatology. 48 (2): 635–45. doi:10.1002/hep.22396. PMID 18666237.
  6. ↑ Jiang F, Yeo CW, Lee SS, Oh MK, Ghim JL, Shon JH, Kim HS, Kim EY, Kim DH, Shin JG (2013). "Effect of HNF4α genetic polymorphism G60D on the pharmacokinetics of CYP2D6 substrate tolterodine in healthy Korean individuals". Pharmacogenetics and Genomics. 23 (3): 175–9. doi:10.1097/FPC.0b013e32835de25e. PMID 23292115.
  7. ↑ Wang ZQ, Lu FE, Leng SH, Fang XS, Chen G, Wang ZS, Dong LP, Yan ZQ (Oct 2008). "Facilitating effects of berberine on rat pancreatic islets through modulating hepatic nuclear factor 4 alpha expression and glucokinase activity". World Journal of Gastroenterology. 14 (39): 6004–11. doi:10.3748/wjg.14.6004. PMC 2760199. PMID 18932278.
  8. ↑ Munkácsy, Gyöngyi; Sztupinszki, Zsófia; Herman, Péter; Bán, Bence; Pénzváltó, Zsófia; Szarvas, Nóra; Győrffy, Balázs (2016-01-01). "Validation of RNAi Silencing Efficiency Using Gene Array Data shows 18.5% Failure Rate across 429 Independent Experiments". Molecular Therapy - Nucleic Acids. 5. doi:10.1038/mtna.2016.66. ISSN 2162-2531. PMC 5056990. PMID 27673562.
  9. ↑ Yamagata K (2014). "Roles of HNF1α and HNF4α in pancreatic β-cells: lessons from a monogenic form of diabetes (MODY)". Vitamins and Hormones. 95: 407–23. doi:10.1016/B978-0-12-800174-5.00016-8. PMID 24559927.
  10. ↑ Zhang B, Wang J, Wang X, Zhu J, Liu Q, Shi Z, et al. (2014). "Proteogenomic characterization of human colon and rectal cancer". Nature. 513 (7518): 382–7. doi:10.1038/nature13438. PMC 4249766. PMID 25043054.
  11. ↑ Mulholland DJ, Read JT, Rennie PS, Cox ME, Nelson CC (Aug 2003). "Functional localization and competition between the androgen receptor and T-cell factor for nuclear beta-catenin: a means for inhibition of the Tcf signaling axis". Oncogene. 22 (36): 5602–13. doi:10.1038/sj.onc.1206802. PMID 12944908.
  12. ↑ Yoshida E, Aratani S, Itou H, Miyagishi M, Takiguchi M, Osumu T, Murakami K, Fukamizu A (Dec 1997). "Functional association between CBP and HNF4 in trans-activation". Biochemical and Biophysical Research Communications. 241 (3): 664–9. doi:10.1006/bbrc.1997.7871. PMID 9434765.
  13. ↑ Dell H, Hadzopoulou-Cladaras M (Mar 1999). "CREB-binding protein is a transcriptional coactivator for hepatocyte nuclear factor-4 and enhances apolipoprotein gene expression". The Journal of Biological Chemistry. 274 (13): 9013–21. doi:10.1074/jbc.274.13.9013. PMID 10085149.
  14. ↑ 14.0 14.1 Maeda Y, Rachez C, Hawel L, Byus CV, Freedman LP, Sladek FM (Jul 2002). "Polyamines modulate the interaction between nuclear receptors and vitamin D receptor-interacting protein 205". Molecular Endocrinology. 16 (7): 1502–10. doi:10.1210/mend.16.7.0883. PMID 12089346.
  15. ↑ 15.0 15.1 Malik S, Wallberg AE, Kang YK, Roeder RG (Aug 2002). "TRAP/SMCC/mediator-dependent transcriptional activation from DNA and chromatin templates by orphan nuclear receptor hepatocyte nuclear factor 4". Molecular and Cellular Biology. 22 (15): 5626–37. doi:10.1128/MCB.22.15.5626-5637.2002. PMC 133960. PMID 12101254.
  16. ↑ Lee YK, Dell H, Dowhan DH, Hadzopoulou-Cladaras M, Moore DD (Jan 2000). "The orphan nuclear receptor SHP inhibits hepatocyte nuclear factor 4 and retinoid X receptor transactivation: two mechanisms for repression". Molecular and Cellular Biology. 20 (1): 187–95. doi:10.1128/MCB.20.1.187-195.2000. PMC 85074. PMID 10594021.
  17. ↑ Lin WJ, Li J, Lee YF, Yeh SD, Altuwaijri S, Ou JH, Chang C (Mar 2003). "Suppression of hepatitis B virus core promoter by the nuclear orphan receptor TR4". The Journal of Biological Chemistry. 278 (11): 9353–60. doi:10.1074/jbc.M205944200. PMID 12522137.

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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