Literature DB >> 1423315

Identification of the eleventh complementation group of UV-sensitive excision repair-defective rodent mutants.

R Riboni1, E Botta, M Stefanini, M Numata, A Yasui.   

Abstract

The drug-sensitive mutant UVS1, isolated from the Chinese hamster cell line CHO9, was previously found to complement the UV sensitivity of the excision repair-defective rodent mutants representative of groups 1 to 8 (Hata et al., Cancer Res., 51: 195-198, 1991; M. Numata et al., personal communication). Recently two new complementation groups of UV-sensitive CHO mutants, e.g., groups 9 and 10, have been identified (Stefanini et al., Cancer Res., 51: 3965-3971, 1991). In this paper we demonstrate that the repair defect in UVS1 cells is genetically different from those present in the mutants CHO7PV and CHO4PV, representing groups 9 and 10, respectively. Therefore, UVS1 represents a new complementation group of UV-sensitive rodent cell lines, the eleventh group.

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Year:  1992        PMID: 1423315

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  9 in total

1.  XPC and human homologs of RAD23: intracellular localization and relationship to other nucleotide excision repair complexes.

Authors:  P J van der Spek; A Eker; S Rademakers; C Visser; K Sugasawa; C Masutani; F Hanaoka; D Bootsma; J H Hoeijmakers
Journal:  Nucleic Acids Res       Date:  1996-07-01       Impact factor: 16.971

2.  ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs.

Authors:  K W Brookman; J E Lamerdin; M P Thelen; M Hwang; J T Reardon; A Sancar; Z Q Zhou; C A Walter; C N Parris; L H Thompson
Journal:  Mol Cell Biol       Date:  1996-11       Impact factor: 4.272

3.  Specific association between the human DNA repair proteins XPA and ERCC1.

Authors:  L Li; S J Elledge; C A Peterson; E S Bales; R J Legerski
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-24       Impact factor: 11.205

4.  Mutations in XPA that prevent association with ERCC1 are defective in nucleotide excision repair.

Authors:  L Li; C A Peterson; X Lu; R J Legerski
Journal:  Mol Cell Biol       Date:  1995-04       Impact factor: 4.272

5.  Molecular cloning of the human nucleotide-excision-repair gene ERCC4.

Authors:  L H Thompson; K W Brookman; C A Weber; E P Salazar; J T Reardon; A Sancar; Z Deng; M J Siciliano
Journal:  Proc Natl Acad Sci U S A       Date:  1994-07-19       Impact factor: 11.205

6.  A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy.

Authors:  M Stefanini; W Vermeulen; G Weeda; S Giliani; T Nardo; M Mezzina; A Sarasin; J I Harper; C F Arlett; J H Hoeijmakers
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

7.  Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.

Authors:  A J van Vuuren; E Appeldoorn; H Odijk; A Yasui; N G Jaspers; D Bootsma; J H Hoeijmakers
Journal:  EMBO J       Date:  1993-09       Impact factor: 11.598

8.  Purification and cloning of a nucleotide excision repair complex involving the xeroderma pigmentosum group C protein and a human homologue of yeast RAD23.

Authors:  C Masutani; K Sugasawa; J Yanagisawa; T Sonoyama; M Ui; T Enomoto; K Takio; K Tanaka; P J van der Spek; D Bootsma
Journal:  EMBO J       Date:  1994-04-15       Impact factor: 11.598

9.  Co-correction of the ERCC1, ERCC4 and xeroderma pigmentosum group F DNA repair defects in vitro.

Authors:  M Biggerstaff; D E Szymkowski; R D Wood
Journal:  EMBO J       Date:  1993-09       Impact factor: 11.598

  9 in total

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