Literature DB >> 2172786

Molecular cloning of the human DNA excision repair gene ERCC-6.

C Troelstra1, H Odijk, J de Wit, A Westerveld, L H Thompson, D Bootsma, J H Hoeijmakers.   

Abstract

The UV-sensitive, nucleotide excision repair-deficient Chinese hamster mutant cell line UV61 was used to identify and clone a correcting human gene, ERCC-6. UV61, belonging to rodent complementation group 6, is only moderately UV sensitive in comparison with mutant lines in groups 1 to 5. It harbors a deficiency in the repair of UV-induced cyclobutane pyrimidine dimers but permits apparently normal repair of (6-4) photoproducts. Genomic (HeLa) DNA transfections of UV61 resulted, with a very low efficiency, in six primary and four secondary UV-resistant transformants having regained wild-type UV survival. Southern blot analysis revealed that five primary and only one secondary transformant retained human sequences. The latter line was used to clone the entire 115-kb human insert. Coinheritance analysis demonstrated that five of the other transformants harbored a 100-kb segment of the cloned human insert. Since it is extremely unlikely that six transformants all retain the same stretch of human DNA by coincidence, we conclude that the ERCC-6 gene resides within this region and probably covers most of it. The large size of the gene explains the extremely low transfection frequency and makes the gene one of the largest cloned by genomic DNA transfection. Four transformants did not retain the correcting ERCC-6 gene and presumably have reverted to the UV-resistant phenotype. One of these appeared to have amplified an endogenous, mutated CHO ERCC-6 allele, indicating that the UV61 mutation is leaky and can be overcome by gene amplification.

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Year:  1990        PMID: 2172786      PMCID: PMC361360          DOI: 10.1128/mcb.10.11.5806-5813.1990

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  41 in total

1.  Toward a physical map of the genome of the nematode Caenorhabditis elegans.

Authors:  A Coulson; J Sulston; S Brenner; J Karn
Journal:  Proc Natl Acad Sci U S A       Date:  1986-10       Impact factor: 11.205

2.  A promising genomic transfectant into Xeroderma pigmentosum group A with highly amplified mouse DNA and intermediate UV resistance turns revertant.

Authors:  M Blum; I Baumann; H Lohrer; H J Rahmsdorf; P Herrlich
Journal:  Biochem Biophys Res Commun       Date:  1989-04-28       Impact factor: 3.575

3.  An eighth complementation group of rodent cells hypersensitive to ultraviolet radiation.

Authors:  L H Thompson; T Shiomi; E P Salazar; S A Stewart
Journal:  Somat Cell Mol Genet       Date:  1988-11

4.  Isolation of UV-sensitive mutants of mouse L5178Y cells by a cell suspension spotting method.

Authors:  T Shiomi; N Hieda-Shiomi; K Sato
Journal:  Somatic Cell Genet       Date:  1982-05

5.  Genetic diversity of UV-sensitive DNA repair mutants of Chinese hamster ovary cells.

Authors:  L H Thompson; D B Busch; K Brookman; C L Mooney; D A Glaser
Journal:  Proc Natl Acad Sci U S A       Date:  1981-06       Impact factor: 11.205

6.  Unique DNA repair properties of a xeroderma pigmentosum revertant.

Authors:  J E Cleaver; F Cortés; L H Lutze; W F Morgan; A N Player; D L Mitchell
Journal:  Mol Cell Biol       Date:  1987-09       Impact factor: 4.272

7.  Hypersensitivity to mutation and sister-chromatid-exchange induction in CHO cell mutants defective in incising DNA containing UV lesions.

Authors:  L H Thompson; K W Brookman; L E Dillehay; C L Mooney; A V Carrano
Journal:  Somatic Cell Genet       Date:  1982-11

8.  Recent progress with the DNA repair mutants of Chinese hamster ovary cells.

Authors:  L H Thompson; E P Salazar; K W Brookman; C C Collins; S A Stewart; D B Busch; C A Weber
Journal:  J Cell Sci Suppl       Date:  1987

Review 9.  Repair of DNA-containing pyrimidine dimers.

Authors:  L Grossman; P R Caron; S J Mazur; E Y Oh
Journal:  FASEB J       Date:  1988-08       Impact factor: 5.191

10.  Microdissection and cloning of DNA from a specific region of Drosophila melanogaster polytene chromosomes.

Authors:  F Scalenghe; E Turco; J E Edström; V Pirrotta; M Melli
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

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  30 in total

1.  Molecular characterization of an acidic region deletion mutant of Cockayne syndrome group B protein.

Authors:  M Sunesen; R R Selzer; R M Brosh; A S Balajee; T Stevnsner; V A Bohr
Journal:  Nucleic Acids Res       Date:  2000-08-15       Impact factor: 16.971

2.  Cloning and characterization of the Drosophila homolog of the xeroderma pigmentosum complementation-group B correcting gene, ERCC3.

Authors:  M H Koken; C Vreeken; S A Bol; N C Cheng; I Jaspers-Dekker; J H Hoeijmakers; J C Eeken; G Weeda; A Pastink
Journal:  Nucleic Acids Res       Date:  1992-11-11       Impact factor: 16.971

Review 3.  Cockayne syndrome: defective repair of transcription?

Authors:  A J van Gool; G T van der Horst; E Citterio; J H Hoeijmakers
Journal:  EMBO J       Date:  1997-07-16       Impact factor: 11.598

4.  Complementation of the DNA repair-deficient swi10 mutant of fission yeast by the human ERCC1 gene.

Authors:  C Rödel; T Jupitz; H Schmidt
Journal:  Nucleic Acids Res       Date:  1997-07-15       Impact factor: 16.971

5.  Molecular and functional analysis of the XPBC/ERCC-3 promoter: transcription activity is dependent on the integrity of an Sp1-binding site.

Authors:  L Ma; G Weeda; A G Jochemsen; D Bootsma; J H Hoeijmakers; A J van der Eb
Journal:  Nucleic Acids Res       Date:  1992-01-25       Impact factor: 16.971

6.  Induction of a mutant phenotype in human repair proficient cells after overexpression of a mutated human DNA repair gene.

Authors:  P B Belt; M F van Oosterwijk; H Odijk; J H Hoeijmakers; C Backendorf
Journal:  Nucleic Acids Res       Date:  1991-10-25       Impact factor: 16.971

7.  Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene.

Authors:  W L Flejter; L D McDaniel; D Johns; E C Friedberg; R A Schultz
Journal:  Proc Natl Acad Sci U S A       Date:  1992-01-01       Impact factor: 11.205

8.  Cockayne syndrome group B protein stimulates repair of formamidopyrimidines by NEIL1 DNA glycosylase.

Authors:  Meltem Muftuoglu; Nadja C de Souza-Pinto; Arin Dogan; Maria Aamann; Tinna Stevnsner; Ivana Rybanska; Güldal Kirkali; Miral Dizdaroglu; Vilhelm A Bohr
Journal:  J Biol Chem       Date:  2009-01-29       Impact factor: 5.157

9.  Accumulation of (5'S)-8,5'-cyclo-2'-deoxyadenosine in organs of Cockayne syndrome complementation group B gene knockout mice.

Authors:  Güldal Kirkali; Nadja C de Souza-Pinto; Pawel Jaruga; Vilhelm A Bohr; Miral Dizdaroglu
Journal:  DNA Repair (Amst)       Date:  2008-11-18

10.  The human CSB (ERCC6) gene corrects the transcription-coupled repair defect in the CHO cell mutant UV61.

Authors:  D K Orren; G L Dianov; V A Bohr
Journal:  Nucleic Acids Res       Date:  1996-09-01       Impact factor: 16.971

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