RECQL4: Difference between revisions

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{{Infobox gene}}
{{PBB_Controls
'''ATP-dependent DNA helicase Q4''' is an [[enzyme]] that in humans is encoded by the ''RECQL4'' [[gene]].<ref name="pmid9878247">{{cite journal | vauthors = Kitao S, Ohsugi I, Ichikawa K, Goto M, Furuichi Y, Shimamoto A | title = Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes | journal = Genomics | volume = 54 | issue = 3 | pages = 443–52 |date=Feb 1999 | pmid = 9878247 | pmc =  | doi = 10.1006/geno.1998.5595 }}</ref><ref name="pmid15960976">{{cite journal | vauthors = Sangrithi MN, Bernal JA, Madine M, Philpott A, Lee J, Dunphy WG, Venkitaraman AR | title = Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome | journal = Cell | volume = 121 | issue = 6 | pages = 887–98 |date=Jun 2005 | pmid = 15960976 | pmc =  | doi = 10.1016/j.cell.2005.05.015 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: RECQL4 RecQ protein-like 4| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=9401| accessdate = }}</ref>
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{{GNF_Protein_box
| image =
| image_source = 
| PDB =
| Name = RecQ protein-like 4
| HGNCid = 9949
| Symbol = RECQL4
| AltSymbols =; RTS; RECQ4
| OMIM = 603780
| ECnumber =
| Homologene = 3144
| MGIid = 1931028
  | GeneAtlas_image1 = PBB_GE_RECQL4_213520_at_tn.png
| Function = {{GNF_GO|id=GO:0000166 |text = nucleotide binding}} {{GNF_GO|id=GO:0003676 |text = nucleic acid binding}} {{GNF_GO|id=GO:0003678 |text = DNA helicase activity}} {{GNF_GO|id=GO:0005524 |text = ATP binding}} {{GNF_GO|id=GO:0008026 |text = ATP-dependent helicase activity}} {{GNF_GO|id=GO:0008270 |text = zinc ion binding}} {{GNF_GO|id=GO:0016787 |text = hydrolase activity}}
| Component = {{GNF_GO|id=GO:0005634 |text = nucleus}}
  | Process = {{GNF_GO|id=GO:0006281 |text = DNA repair}} {{GNF_GO|id=GO:0006310 |text = DNA recombination}} {{GNF_GO|id=GO:0007275 |text = multicellular organismal development}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 9401
    | Hs_Ensembl = ENSG00000160957
    | Hs_RefseqProtein = NP_004251
    | Hs_RefseqmRNA = NM_004260
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 8
    | Hs_GenLoc_start = 145707480
    | Hs_GenLoc_end = 145713976
    | Hs_Uniprot = O94761
    | Mm_EntrezGene = 79456
    | Mm_Ensembl = ENSMUSG00000033762
    | Mm_RefseqmRNA = XM_903254
    | Mm_RefseqProtein = XP_908347
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 15
    | Mm_GenLoc_start = 76530815
    | Mm_GenLoc_end = 76537803
    | Mm_Uniprot = Q75NR7
  }}
}}
'''RecQ protein-like 4''', also known as '''RECQL4''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: RECQL4 RecQ protein-like 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=9401| accessdate = }}</ref>
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Mutations in ''RECQL4'' are associated with the autosomal recessive disease [[Rothmund-Thomson Syndrome]].  There are two types of Rothmund Thomson syndrome and it is Type 2 that is caused by patients carrying deleterious mutations in both copies of the RECQL4 gene.  This condition is associated with a high risk of developing [[osteosarcoma]] (malignant tumor of the bone).<ref>{{cite journal | author=Wang LL, Gannavarapu A, Kozinetz CA, ''et al.'' |title=Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome. |journal=J. Natl. Cancer Inst. |volume=95 |issue= 9 |pages= 669-74 |year= 2003 |pmid= 12734318 |doi=  }}</ref>
Mutations in ''RECQL4'' are associated with the autosomal recessive disease [[Rothmund-Thomson Syndrome]], a disorder that has features of premature aging.<ref name="pmid24832598">{{cite journal |vauthors=Lu H, Fang EF, Sykora P, Kulikowicz T, Zhang Y, Becker KG, Croteau DL, Bohr VA |title=Senescence induced by RECQL4 dysfunction contributes to Rothmund-Thomson syndrome features in mice |journal=Cell Death Dis |volume=5 |issue= |pages=e1226 |year=2014 |pmid=24832598 |pmc=4047874 |doi=10.1038/cddis.2014.168 |url=}}</ref><ref name="pmid27287744">{{cite journal |vauthors=Lu L, Jin W, Wang LL |title=Aging in Rothmund-Thomson syndrome and related RECQL4 genetic disorders |journal=Ageing Res. Rev. |volume=33 |issue= |pages=30–35 |year=2017 |pmid=27287744 |doi=10.1016/j.arr.2016.06.002 |url=}}</ref>  In addition to the [[Rothmund-Thomson syndrome]], ''RECQL4'' mutations are also associated with [[Rapadilino syndrome|RAPADILINO]] and [[Baller-Gerold syndrome]]s.<ref name="pmid24942867">{{cite journal |vauthors=Shamanna RA, Singh DK, Lu H, Mirey G, Keijzers G, Salles B, Croteau DL, Bohr VA |title=RECQ helicase RECQL4 participates in non-homologous end joining and interacts with the Ku complex |journal=Carcinogenesis |volume=35 |issue=11 |pages=2415–24 |year=2014 |pmid=24942867 |pmc=4216052 |doi=10.1093/carcin/bgu137 |url=}}</ref> There are two types of Rothmund Thomson syndrome and it is Type 2 that occurs in patients carrying deleterious mutations in both copies of the ''RECQL4'' gene.  This condition is associated with a high risk of developing [[osteosarcoma]] (malignant tumor of the bone).<ref>{{cite journal   |vauthors=Wang LL, Gannavarapu A, Kozinetz CA, etal |title=Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome. |journal=J. Natl. Cancer Inst. |volume=95 |issue= 9 |pages= 669–74 |year= 2003 |pmid= 12734318 |doi=10.1093/jnci/95.9.669 }}</ref>
''RECQL4'' gets it name from being homologous (sharing sequence) with other members of the [[RecQ helicase]] family.  Two other genetic diseases are due to mutations in other RECQ helicases. [[Bloom syndrome]] is associated with mutations in the ''BLM'' gene and [[Werner syndrome]] is associated with mutations in the ''WRN'' gene.<ref>{{cite journal | author=Kitao S, Lindor NM, Shiratori M, ''et al.'' |title=Rothmund-thomson syndrome responsible gene, RECQL4: genomic structure and products. |journal=Genomics |volume=61 |issue= 3 |pages= 268-76 |year= 2000 |pmid= 10552928 |doi= 10.1006/geno.1999.5959 }}</ref>
''RECQL4'' gets its name from being homologous (sharing sequence) with other members of the [[RecQ helicase]] family.  Two other genetic diseases are due to mutations in other RECQ helicases. [[Bloom syndrome]] is associated with mutations in the ''BLM'' gene and [[Werner syndrome]] is associated with mutations in the ''WRN'' gene.<ref>{{cite journal   |vauthors=Kitao S, Lindor NM, Shiratori M, etal |title=Rothmund-thomson syndrome responsible gene, RECQL4: genomic structure and products. |journal=Genomics |volume=61 |issue= 3 |pages= 268–76 |year= 2000 |pmid= 10552928 |doi= 10.1006/geno.1999.5959 }}</ref>
 
==DNA repair==
 
[[Double-strand breaks]] in DNA are potentially lethal to a cell and need to be repaired.  Repair of double-strand breaks by [[homologous recombination]] (HR) is an important cellular mechanism for avoiding this lethality.  RECQL4 has a crucial role in the first step of HR, referred to as end resection.<ref name="pmid27320928">{{cite journal |vauthors=Lu H, Shamanna RA, Keijzers G, Anand R, Rasmussen LJ, Cejka P, Croteau DL, Bohr VA |title=RECQL4 Promotes DNA End Resection in Repair of DNA Double-Strand Breaks |journal=Cell Rep |volume=16 |issue=1 |pages=161–73 |year=2016 |pmid=27320928 |doi=10.1016/j.celrep.2016.05.079 |url=}}</ref>  When RECQL4 is deficient, end resection, and thus HR, is reduced.  Evidence suggests that other forms of DNA repair including [[non-homologous end joining]], [[nucleotide excision repair]] and [[base excision repair]] also depend on RECQL4 function.<ref name="pmid27287744" />  In the Rothmund-Thomson syndrome, the association of deficient RECQL4-mediated DNA repair and premature aging is consistent with the [[DNA damage theory of aging]].


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


==Further reading==
==Further reading==
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{{PBB_Further_reading  
{{PBB_Further_reading  
| citations =  
| citations =  
*{{cite journal  | author=Kellermayer R |title=The versatile RECQL4. |journal=Genet. Med. |volume=8 |issue= 4 |pages= 213-6 |year= 2006 |pmid= 16617241 |doi= 10.1097/01.gim.0000214457.58378.1a }}
*{{cite journal  | author=Kellermayer R |title=The versatile RECQL4. |journal=Genet. Med. |volume=8 |issue= 4 |pages= 213–6 |year= 2006 |pmid= 16617241 |doi= 10.1097/01.gim.0000214457.58378.1a }}
*{{cite journal  | author=Soukup T |title=Intrafusal fibre types in rat limb muscle spindles: morphological and histochemical characteristics. |journal=Histochemistry |volume=47 |issue= 1 |pages= 43-57 |year= 1976 |pmid= 133085 |doi=  }}
*{{cite journal  | author=Soukup T |title=Intrafusal fibre types in rat limb muscle spindles: morphological and histochemical characteristics. |journal=Histochemistry |volume=47 |issue= 1 |pages= 43–57 |year= 1976 |pmid= 133085 |doi=10.1007/BF00492992  }}
*{{cite journal  | author=Kitao S, Ohsugi I, Ichikawa K, ''et al.'' |title=Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes. |journal=Genomics |volume=54 |issue= 3 |pages= 443-52 |year= 1999 |pmid= 9878247 |doi= 10.1006/geno.1998.5595 }}
*{{cite journal   |vauthors=Kitao S, Shimamoto A, Goto M, etal |title=Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome. |journal=Nat. Genet. |volume=22 |issue= 1 |pages= 82–4 |year= 1999 |pmid= 10319867 |doi= 10.1038/8788 }}
*{{cite journal | author=Kitao S, Shimamoto A, Goto M, ''et al.'' |title=Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome. |journal=Nat. Genet. |volume=22 |issue= 1 |pages= 82-4 |year= 1999 |pmid= 10319867 |doi= 10.1038/8788 }}
*{{cite journal  | vauthors=Yankiwski V, Marciniak RA, Guarente L, Neff NF |title=Nuclear structure in normal and Bloom syndrome cells. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=97 |issue= 10 |pages= 5214–9 |year= 2000 |pmid= 10779560 |doi= 10.1073/pnas.090525897 | pmc=25808 }}
*{{cite journal  | author=Yankiwski V, Marciniak RA, Guarente L, Neff NF |title=Nuclear structure in normal and Bloom syndrome cells. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=97 |issue= 10 |pages= 5214-9 |year= 2000 |pmid= 10779560 |doi= 10.1073/pnas.090525897 }}
*{{cite journal   |vauthors=Kawabe T, Tsuyama N, Kitao S, etal |title=Differential regulation of human RecQ family helicases in cell transformation and cell cycle. |journal=Oncogene |volume=19 |issue= 41 |pages= 4764–72 |year= 2000 |pmid= 11032027 |doi= 10.1038/sj.onc.1203841 }}
*{{cite journal | author=Kawabe T, Tsuyama N, Kitao S, ''et al.'' |title=Differential regulation of human RecQ family helicases in cell transformation and cell cycle. |journal=Oncogene |volume=19 |issue= 41 |pages= 4764-72 |year= 2000 |pmid= 11032027 |doi= 10.1038/sj.onc.1203841 }}
*{{cite journal   |vauthors=Wang LL, Worley K, Gannavarapu A, etal |title=Intron-size constraint as a mutational mechanism in Rothmund-Thomson syndrome. |journal=Am. J. Hum. Genet. |volume=71 |issue= 1 |pages= 165–7 |year= 2002 |pmid= 12016592 |doi=10.1086/341234  | pmc=384974 }}
*{{cite journal | author=Wang LL, Worley K, Gannavarapu A, ''et al.'' |title=Intron-size constraint as a mutational mechanism in Rothmund-Thomson syndrome. |journal=Am. J. Hum. Genet. |volume=71 |issue= 1 |pages= 165-7 |year= 2002 |pmid= 12016592 |doi=  }}
*{{cite journal   |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 }}
*{{cite journal | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
*{{cite journal   |vauthors=Roversi G, Beghini A, Zambruno G, etal |title=Identification of two novel RECQL4exonic SNPs and genomic characterization of the IVS12 minisatellite. |journal=J. Hum. Genet. |volume=48 |issue= 2 |pages= 107–9 |year= 2003 |pmid= 12601557 |doi= 10.1007/s100380300016 }}
*{{cite journal | author=Roversi G, Beghini A, Zambruno G, ''et al.'' |title=Identification of two novel RECQL4exonic SNPs and genomic characterization of the IVS12 minisatellite. |journal=J. Hum. Genet. |volume=48 |issue= 2 |pages= 107-9 |year= 2003 |pmid= 12601557 |doi= 10.1007/s100380300016 }}
*{{cite journal   |vauthors=Wang LL, Gannavarapu A, Clericuzio CL, etal |title=Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patients. |journal=Am. J. Med. Genet. A |volume=118 |issue= 3 |pages= 299–301 |year= 2004 |pmid= 12673665 |doi= 10.1002/ajmg.a.10057 }}
*{{cite journal | author=Wang LL, Gannavarapu A, Clericuzio CL, ''et al.'' |title=Absence of RECQL4 mutations in poikiloderma with neutropenia in Navajo and non-Navajo patients. |journal=Am. J. Med. Genet. A |volume=118 |issue= 3 |pages= 299-301 |year= 2004 |pmid= 12673665 |doi= 10.1002/ajmg.a.10057 }}
*{{cite journal   |vauthors=Beghini A, Castorina P, Roversi G, etal |title=RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patient. |journal=Am. J. Med. Genet. A |volume=120 |issue= 3 |pages= 395–9 |year= 2004 |pmid= 12838562 |doi= 10.1002/ajmg.a.20154 }}
*{{cite journal | author=Beghini A, Castorina P, Roversi G, ''et al.'' |title=RNA processing defects of the helicase gene RECQL4 in a compound heterozygous Rothmund-Thomson patient. |journal=Am. J. Med. Genet. A |volume=120 |issue= 3 |pages= 395-9 |year= 2004 |pmid= 12838562 |doi= 10.1002/ajmg.a.20154 }}
*{{cite journal   |vauthors=Siitonen HA, Kopra O, Kääriäinen H, etal |title=Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases. |journal=Hum. Mol. Genet. |volume=12 |issue= 21 |pages= 2837–44 |year= 2004 |pmid= 12952869 |doi= 10.1093/hmg/ddg306 }}
*{{cite journal | author=Siitonen HA, Kopra O, Kääriäinen H, ''et al.'' |title=Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases. |journal=Hum. Mol. Genet. |volume=12 |issue= 21 |pages= 2837-44 |year= 2004 |pmid= 12952869 |doi= 10.1093/hmg/ddg306 }}
*{{cite journal   |vauthors=Brandenberger R, Wei H, Zhang S, etal |title=Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation. |journal=Nat. Biotechnol. |volume=22 |issue= 6 |pages= 707–16 |year= 2005 |pmid= 15146197 |doi= 10.1038/nbt971 }}
*{{cite journal | author=Brandenberger R, Wei H, Zhang S, ''et al.'' |title=Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation. |journal=Nat. Biotechnol. |volume=22 |issue= 6 |pages= 707-16 |year= 2005 |pmid= 15146197 |doi= 10.1038/nbt971 }}
*{{cite journal   |vauthors=Nishijo K, Nakayama T, Aoyama T, etal |title=Mutation analysis of the RECQL4 gene in sporadic osteosarcomas. |journal=Int. J. Cancer |volume=111 |issue= 3 |pages= 367–72 |year= 2004 |pmid= 15221963 |doi= 10.1002/ijc.20269 }}
*{{cite journal | author=Nishijo K, Nakayama T, Aoyama T, ''et al.'' |title=Mutation analysis of the RECQL4 gene in sporadic osteosarcomas. |journal=Int. J. Cancer |volume=111 |issue= 3 |pages= 367-72 |year= 2004 |pmid= 15221963 |doi= 10.1002/ijc.20269 }}
*{{cite journal  | vauthors=Yin J, Kwon YT, Varshavsky A, Wang W |title=RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway. |journal=Hum. Mol. Genet. |volume=13 |issue= 20 |pages= 2421–30 |year= 2005 |pmid= 15317757 |doi= 10.1093/hmg/ddh269 }}
*{{cite journal  | author=Yin J, Kwon YT, Varshavsky A, Wang W |title=RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway. |journal=Hum. Mol. Genet. |volume=13 |issue= 20 |pages= 2421-30 |year= 2005 |pmid= 15317757 |doi= 10.1093/hmg/ddh269 }}
*{{cite journal   |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 }}
*{{cite journal | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }}
*{{cite journal   |vauthors=Sengupta S, Shimamoto A, Koshiji M, etal |title=Tumor suppressor p53 represses transcription of RECQ4 helicase. |journal=Oncogene |volume=24 |issue= 10 |pages= 1738–48 |year= 2005 |pmid= 15674334 |doi= 10.1038/sj.onc.1208380 }}
*{{cite journal | author=Sengupta S, Shimamoto A, Koshiji M, ''et al.'' |title=Tumor suppressor p53 represses transcription of RECQ4 helicase. |journal=Oncogene |volume=24 |issue= 10 |pages= 1738-48 |year= 2005 |pmid= 15674334 |doi= 10.1038/sj.onc.1208380 }}
*{{cite journal  | author=Sangrithi MN, Bernal JA, Madine M, ''et al.'' |title=Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome. |journal=Cell |volume=121 |issue= 6 |pages= 887-98 |year= 2005 |pmid= 15960976 |doi= 10.1016/j.cell.2005.05.015 }}
}}
}}
{{refend}}
{{refend}}


{{protein-stub}}
==External links==
{{WikiDoc Sources}}
* [https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=rts  GeneReviews/NCBI/NIH/UW entry on Rothmund-Thomson Syndrome]
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Latest revision as of 08:43, 10 January 2019

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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RefSeq (mRNA)

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Wikidata
View/Edit Human

ATP-dependent DNA helicase Q4 is an enzyme that in humans is encoded by the RECQL4 gene.[1][2][3]

Mutations in RECQL4 are associated with the autosomal recessive disease Rothmund-Thomson Syndrome, a disorder that has features of premature aging.[4][5] In addition to the Rothmund-Thomson syndrome, RECQL4 mutations are also associated with RAPADILINO and Baller-Gerold syndromes.[6] There are two types of Rothmund Thomson syndrome and it is Type 2 that occurs in patients carrying deleterious mutations in both copies of the RECQL4 gene. This condition is associated with a high risk of developing osteosarcoma (malignant tumor of the bone).[7] RECQL4 gets its name from being homologous (sharing sequence) with other members of the RecQ helicase family. Two other genetic diseases are due to mutations in other RECQ helicases. Bloom syndrome is associated with mutations in the BLM gene and Werner syndrome is associated with mutations in the WRN gene.[8]

DNA repair

Double-strand breaks in DNA are potentially lethal to a cell and need to be repaired. Repair of double-strand breaks by homologous recombination (HR) is an important cellular mechanism for avoiding this lethality. RECQL4 has a crucial role in the first step of HR, referred to as end resection.[9] When RECQL4 is deficient, end resection, and thus HR, is reduced. Evidence suggests that other forms of DNA repair including non-homologous end joining, nucleotide excision repair and base excision repair also depend on RECQL4 function.[5] In the Rothmund-Thomson syndrome, the association of deficient RECQL4-mediated DNA repair and premature aging is consistent with the DNA damage theory of aging.

References

  1. ↑ Kitao S, Ohsugi I, Ichikawa K, Goto M, Furuichi Y, Shimamoto A (Feb 1999). "Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes". Genomics. 54 (3): 443–52. doi:10.1006/geno.1998.5595. PMID 9878247.
  2. ↑ Sangrithi MN, Bernal JA, Madine M, Philpott A, Lee J, Dunphy WG, Venkitaraman AR (Jun 2005). "Initiation of DNA replication requires the RECQL4 protein mutated in Rothmund-Thomson syndrome". Cell. 121 (6): 887–98. doi:10.1016/j.cell.2005.05.015. PMID 15960976.
  3. ↑ "Entrez Gene: RECQL4 RecQ protein-like 4".
  4. ↑ Lu H, Fang EF, Sykora P, Kulikowicz T, Zhang Y, Becker KG, Croteau DL, Bohr VA (2014). "Senescence induced by RECQL4 dysfunction contributes to Rothmund-Thomson syndrome features in mice". Cell Death Dis. 5: e1226. doi:10.1038/cddis.2014.168. PMC 4047874. PMID 24832598.
  5. ↑ 5.0 5.1 Lu L, Jin W, Wang LL (2017). "Aging in Rothmund-Thomson syndrome and related RECQL4 genetic disorders". Ageing Res. Rev. 33: 30–35. doi:10.1016/j.arr.2016.06.002. PMID 27287744.
  6. ↑ Shamanna RA, Singh DK, Lu H, Mirey G, Keijzers G, Salles B, Croteau DL, Bohr VA (2014). "RECQ helicase RECQL4 participates in non-homologous end joining and interacts with the Ku complex". Carcinogenesis. 35 (11): 2415–24. doi:10.1093/carcin/bgu137. PMC 4216052. PMID 24942867.
  7. ↑ Wang LL, Gannavarapu A, Kozinetz CA, et al. (2003). "Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome". J. Natl. Cancer Inst. 95 (9): 669–74. doi:10.1093/jnci/95.9.669. PMID 12734318.
  8. ↑ Kitao S, Lindor NM, Shiratori M, et al. (2000). "Rothmund-thomson syndrome responsible gene, RECQL4: genomic structure and products". Genomics. 61 (3): 268–76. doi:10.1006/geno.1999.5959. PMID 10552928.
  9. ↑ Lu H, Shamanna RA, Keijzers G, Anand R, Rasmussen LJ, Cejka P, Croteau DL, Bohr VA (2016). "RECQL4 Promotes DNA End Resection in Repair of DNA Double-Strand Breaks". Cell Rep. 16 (1): 161–73. doi:10.1016/j.celrep.2016.05.079. PMID 27320928.

Further reading

External links


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