Citations for
1ERCC4, MUS81
Regulation of Structure-Specific Endonucleases in Replication Stress.
Kim SM, Forsburg SL.
Genes (Basel) 9(12). pii: E634. doi: 10.3390/genes9120634. Review. 2018
2DCLRE1C, ERCC1, ERCC4, MUS81
DNA replication stress triggers rapid DNA replication fork breakage by Artemis and XPF.
Bétous R, Goullet de Rugy T, Pelegrini AL, Queille S, de Villartay JP, Hoffmann JS.
PLoS Genet 14(7):e1007541. doi: 10.1371/journal.pgen.1007541. eCollection 2018 Jul. 2018
3ERCC4, FANCQ
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia.
Bogliolo M, Schuster B, Stoepker C, Derkunt B, Su Y, Raams A, Trujillo JP, Minguillón J, Ramírez MJ, Pujol R, Casado JA, Baños R, Rio P, Knies K, Zúñiga S, Benítez J, Bueren JA, Jaspers NG, Schärer OD, de Winter JP, Schindler D, Surrallés J.
Am J Hum Genet 92(5):800-6. doi: 10.1016/j.ajhg.2013.04.002. Epub 2013 Apr 25. 2013
4COFS4, ERCC1, ERCC4, XFEP
Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia.
Kashiyama K, Nakazawa Y, Pilz DT, Guo C, Shimada M, Sasaki K, Fawcett H, Wing JF, Lewin SO, Carr L, Li TS, Yoshiura K, Utani A, Hirano A, Yamashita S, Greenblatt D, Nardo T, Stefanini M, McGibbon D, Sarkany R, Fassihi H, Takahashi Y, Nagayama Y, Mitsutake N, Lehmann AR, Ogi T.
Am J Hum Genet 92(5):807-19. doi: 10.1016/j.ajhg.2013.04.007. Epub 2013 Apr 25. 2013
5ERCC4, ERCC5
XPG and XPF endonucleases trigger chromatin looping and DNA demethylation for accurate expression of activated genes.
Le May N, Fradin D, Iltis I, Bougnères P, Egly JM.
Mol Cell 47(4):622-32. doi: 10.1016/j.molcel.2012.05.050. Epub 2012 Jul 5. 2012
6ERCC4
Association between single nucleotide polymorphisms in ERCC4 and risk of squamous cell carcinoma of the head and neck.
Yu H, Liu Z, Huang YJ, Yin M, Wang LE, Wei Q.
PLoS One 7(7):e41853. doi: 10.1371/journal.pone.0041853. Epub 2012 Jul 27. 2012
7ERCC1, ERCC4
Multiple DNA binding domains mediate the function of the ERCC1-XPF protein in nucleotide excision repair.
Su Y, Orelli B, Madireddy A, Niedernhofer LJ, Schärer OD.
J Biol Chem 287(26):21846-55. doi: 10.1074/jbc.M111.337899. Epub 2012 Apr 30. 2012
8DCLRE1A, ERCC1, ERCC4
Human SNM1A and XPF-ERCC1 collaborate to initiate DNA interstrand cross-link repair.
Wang AT, Sengerová B, Cattell E, Inagawa T, Hartley JM, Kiakos K, Burgess-Brown NA, Swift LP, Enzlin JH, Schofield CJ, Gileadi O, Hartley JA, McHugh PJ.
Genes Dev 25(17):1859-70. 2011
9ERCC1, ERCC4, XPF
Mislocalization of XPF-ERCC1 nuclease contributes to reduced DNA repair in XP-F patients.
Ahmad A, Enzlin JH, Bhagwat NR, Wijgers N, Raams A, Appledoorn E, Theil AF, J Hoeijmakers JH, Vermeulen W, J Jaspers NG, Schärer OD, Niedernhofer LJ.
PLoS Genet 6(3):e1000871. 2010
10ERCC1, ERCC4
The ERCC1/XPF endonuclease is required for completion of homologous recombination at DNA replication forks stalled by inter-strand cross-links.
Al-Minawi AZ, Lee YF, Håkansson D, Johansson F, Lundin C, Saleh-Gohari N, Schultz N, Jenssen D, Bryant HE, Meuth M, Hinz JM, Helleday T.
Nucleic Acids Res 37(19):6400-13. Epub 2009 Aug 27. 2009
11ERCC4
Polymorphisms in excision repair cross-complementing group 4 (ERCC4) and susceptibility to primary lung cancer in a Chinese Han population.
Shao M, Ma H, Wang Y, Xu L, Yuan J, Wang Y, Hu Z, Yang L, Wang F, Liu H, Qian J, Xun P, Chen W, Yuan W, Jing G, Chen F, Jin L, Wei Q, Wu T, Shen H, Huang W, Lu D.
Lung Cancer 60(3):332-9. Epub 2008 Feb 20. 2008
12EME1, EME2, ERCC1, ERCC4, FAAP24, FANCM, MUS81
Identification of FAAP24, a Fanconi anemia core complex protein that interacts with FANCM.
Ciccia A, Ling C, Coulthard R, Yan Z, Xue Y, Meetei AR, Laghmani el H, Joenje H, McDonald N, de Winter JP, Wang W, West SC.
Mol Cell 25(3):331-43. 2007
13ERCC1, ERCC4
DNA repair gene polymorphisms and genetic predisposition to cutaneous melanoma.
Povey JE, Darakhshan F, Robertson K, Bisset Y, Mekky M, Rees J, Doherty V, Kavanagh G, Anderson N, Campbell H, MacKie RM, Melton DW.
Carcinogenesis 28(5):1087-93. Epub 2007 Jan 8. 2007
14ERCC4, XFEP
A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis.
Niedernhofer LJ, Garinis GA, Raams A, Lalai AS, Robinson AR, Appeldoorn E, Odijk H, Oostendorp R, Ahmad A, van Leeuwen W, Theil AF, Vermeulen W, van der Horst GT, Meinecke P, Kleijer WJ, Vijg J, Jaspers NG, Hoeijmakers JH.
Nature 444(7122):1038-43. 2006
15ERCC4, TERF2
XPF nuclease-dependent telomere loss and increased DNA damage in mice overexpressing TRF2 result in premature aging and cancer.
Munoz P, Blanco R, Flores JM, Blasco MA.
Nat Genet 37(10):1063-71. Epub 2005 Sep 4. 2005
16RAD52, ERCC4
Physical and functional interaction between the XPF/ERCC1 endonuclease and hRad52.
Motycka TA, Bessho T, Post SM, Sung P, Tomkinson AE.
J Biol Chem 279(14):13634-9. Epub 2004 Jan 20. 2004
17DDB1, DDB2, ERCC2, ERCC3, ERCC4, ERCC5, XPA, XPC
Clusters of transcription-coupled repair in the human genome.
Surralles J, Ramirez MJ, Marcos R, Natarajan AT, Mullenders LH.
Proc Natl Acad Sci U S A 99(16):10571-4. 2002
18ERCC1, ERCC4, XPF
Activity of individual ERCC1 and XPF subunits in DNA nucleotide excision repair.
Gaillard PH, Wood RD.
Nucleic Acids Res 29(4):872-9. 2001
19ERCC4
Quantitative determination of the expression of xeroderma pigmentosum F gene in human nonmelanoma skin cancers.
Chang LC, Sheu HM, Huang YS, Kuo KW.
Biochem Biophys Res Commun 273(2):454-8. 2000
20ERCC4
Conserved domains in DNA repair proteins and evolution of repair systems.
Aravind L, et al.
Nucleic Acids Res 27(5):1223-1242. 1999
21ERCC4
Domain mapping of the DNA binding, endonuclease, and ERCC1 binding properties of the human DNA repair protein XPF.
McCutchen-Maloney SL, et al.
Biochemistry 38(29):9417-25 1999
22ERCC4, XPF
Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease.
Sijbers AM, et al.
J Invest Dermatol 110 : 832-836. 1998
23ERCC1, ERCC4, XPF
Mapping of interaction domains between human repair proteins ERCC1 and XPF.
de Laat WL, Sijbers AM, Odijk H, Jaspers NG, Hoeijmakers JH.
Nucleic Acids Res 26 : 4146-4152. 1998
24ERCC4, XPF
Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease.
Sijbers AM, et al.
Cell 86 : 811-822. 1996
25ERCC4
ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs.
Brookman KW, Lamerdin JE, Thelen MP, Hwang M, Reardon JT, Sancar A, Zhou ZQ, Walter CA, Parris CN, Thompson LH.
Mol Cell Biol 16(11):6553-62. 1996
26ERCC4
Molecular cloning of the human nucleotide-excision-repair gene ERCC4.
Thompson LH, et al.
Proc Natl Acad Sci U S A 91 : 6855-6859. 1994
27ERCC1, ERCC4
Specific cleavage of model recombination and repair intermediates by the yeast Rad1-Rad10 DNA endonuclease.
Bardwell AJ, et al.
Science 265 : 2082-2085. 1994
28ERCC4
Regional mapping of human DNA excision repair gene ERCC4 to chromosome 16p13.13-p13.2.
Liu P, et al.
Mutagenesis 8 : 199-205. 1993
29ERCC1, ERCC4, ERCC5
Co-correction of the ERCC1, ERCC4 and xeroderma pigmentosum group F DNA repair defects in vitro.
Biggerstaff M, et al.
EMBO J 12 : 3685-3692. 1993
30ERCC1, ERCC4, ERCC5, XPF
Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.
Van Vuuren AJ, et al.
EMBO J 12 : 3693-3701. 1993
31ERCC4, XPC
Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes.
Venema J, van Hoffen A, Karcagi V, Natarajan AT, van Zeeland AA, Mullenders LH.
Mol Cell Biol 11(8):4128-34. 1991
32ERCC4, D16S213, D16S214, D16S215
Human DNA excision repair gene ERCC4 is located on chromosome 16 short arm 16p13.13-p13.3.
Liu P, et al.
(HGM10) Cytogenet Cell Genet 51 : 1035. 1989
33ERCC3, ERCC4, ERCC5, XRCC1
Chromosomal assignments of human DNA repair genes that complement chinese hamster ovary (CHO) cell mutants.
Siciliano MJ, et al.
(HGM9) Cytogenet Cell Genet 46 : 691. 1987
34ERCC3, ERCC4
Assignment of a human DNA repair gene associated with sister-chromatid exchange to chromosome 19.
Siciliano MJ, et al.
Mutat Res 174 : 303-308. 1986