Literature DB >> 7510366

An ERCC5 gene with homology to yeast RAD2 is involved in group G xeroderma pigmentosum.

T Shiomi1, Y Harada, T Saito, N Shiomi, Y Okuno, M Yamaizumi.   

Abstract

We have isolated a human excision repair gene ERCC5 which complements the defect of the mouse UV-sensitive mutant XL216 (rodent complementation group 5). Here we report cDNA cloning of human and mouse ERCC5 genes using an exon containing an ERCC5 fragment as a probe. The ERCC5 cDNA encodes a predicted 133-kDa nuclear protein that shares some homology with the product of the yeast DNA repair gene RAD2. Transfection with mouse ERCC5 cDNA restored normal levels of UV resistance to XL216 cells. Microinjection of ERCC5 cDNA specifically restored the defect of xeroderma pigmentosum group G cells (XP-G) as measured by unscheduled DNA synthesis, and XP-G cells stably transformed with ERCC5 cDNA showed nearly normal UV resistance.

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Year:  1994        PMID: 7510366     DOI: 10.1016/0921-8777(94)90080-9

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  12 in total

1.  Active-site mutations in the Xrn1p exoribonuclease of Saccharomyces cerevisiae reveal a specific role in meiosis.

Authors:  J A Solinger; D Pascolini; W D Heyer
Journal:  Mol Cell Biol       Date:  1999-09       Impact factor: 4.272

2.  Molecular cloning and structural analysis of the functional mouse genomic XPG gene.

Authors:  D L Ludwig; J S Mudgett; M S Park; A V Perez-Castro; M A MacInnes
Journal:  Mamm Genome       Date:  1996-09       Impact factor: 2.957

3.  Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populations.

Authors:  Jing He; Li-Xin Qiu; Meng-Yun Wang; Rui-Xi Hua; Ruo-Xin Zhang; Hong-Ping Yu; Ya-Nong Wang; Meng-Hong Sun; Xiao-Yan Zhou; Ya-Jun Yang; Jiu-Cun Wang; Li Jin; Qing-Yi Wei; Jin Li
Journal:  Hum Genet       Date:  2012-02-28       Impact factor: 4.132

4.  Ultraviolet-induced movement of the human DNA repair protein, Xeroderma pigmentosum type G, in the nucleus.

Authors:  M S Park; J A Knauf; S H Pendergrass; C H Coulon; G F Strniste; B L Marrone; M A MacInnes
Journal:  Proc Natl Acad Sci U S A       Date:  1996-08-06       Impact factor: 11.205

5.  The human XPG gene: gene architecture, alternative splicing and single nucleotide polymorphisms.

Authors:  S Emmert; T D Schneider; S G Khan; K H Kraemer
Journal:  Nucleic Acids Res       Date:  2001-04-01       Impact factor: 16.971

6.  A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function.

Authors:  T Nouspikel; P Lalle; S A Leadon; P K Cooper; S G Clarkson
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-01       Impact factor: 11.205

7.  Postnatal growth failure, short life span, and early onset of cellular senescence and subsequent immortalization in mice lacking the xeroderma pigmentosum group G gene.

Authors:  Y N Harada; N Shiomi; M Koike; M Ikawa; M Okabe; S Hirota; Y Kitamura; M Kitagawa; T Matsunaga; O Nikaido; T Shiomi
Journal:  Mol Cell Biol       Date:  1999-03       Impact factor: 4.272

8.  Identification of the XPG region that causes the onset of Cockayne syndrome by using Xpg mutant mice generated by the cDNA-mediated knock-in method.

Authors:  Naoko Shiomi; Seiji Kito; Masaki Oyama; Tsukasa Matsunaga; Yoshi-Nobu Harada; Masahito Ikawa; Masaru Okabe; Tadahiro Shiomi
Journal:  Mol Cell Biol       Date:  2004-05       Impact factor: 4.272

9.  An XPG DNA repair defect causing mutagen hypersensitivity in mouse leukemia L1210 cells.

Authors:  J A Vilpo; L M Vilpo; D E Szymkowski; A O'Donovan; R D Wood
Journal:  Mol Cell Biol       Date:  1995-01       Impact factor: 4.272

10.  Genome-wide association analysis of oxidative stress resistance in Drosophila melanogaster.

Authors:  Allison L Weber; George F Khan; Michael M Magwire; Crystal L Tabor; Trudy F C Mackay; Robert R H Anholt
Journal:  PLoS One       Date:  2012-04-04       Impact factor: 3.240

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