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

C. Troelstra, H. Odijk, J. De Wit, A. Westerveld, L. H. Thompson, D. Bootsma, J. H J Hoeijmakers

Research output: Contribution to journalArticle

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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.

Original languageEnglish (US)
Pages (from-to)5806-5813
Number of pages8
JournalMolecular and Cellular Biology
Volume10
Issue number11
StatePublished - 1990
Externally publishedYes

Fingerprint

Molecular Cloning
DNA Repair
Transfection
Genes
DNA
Clone Cells
Pyrimidine Dimers
Gene Amplification
Southern Blotting
Cricetulus
Gene Frequency
Rodentia
Alleles
Phenotype
Cell Line
Mutation
Survival

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cell Biology

Cite this

Troelstra, C., Odijk, H., De Wit, J., Westerveld, A., Thompson, L. H., Bootsma, D., & Hoeijmakers, J. H. J. (1990). Molecular cloning of the human DNA excision repair gene ERCC-6. Molecular and Cellular Biology, 10(11), 5806-5813.

Molecular cloning of the human DNA excision repair gene ERCC-6. / Troelstra, C.; Odijk, H.; De Wit, J.; Westerveld, A.; Thompson, L. H.; Bootsma, D.; Hoeijmakers, J. H J.

In: Molecular and Cellular Biology, Vol. 10, No. 11, 1990, p. 5806-5813.

Research output: Contribution to journalArticle

Troelstra, C, Odijk, H, De Wit, J, Westerveld, A, Thompson, LH, Bootsma, D & Hoeijmakers, JHJ 1990, 'Molecular cloning of the human DNA excision repair gene ERCC-6', Molecular and Cellular Biology, vol. 10, no. 11, pp. 5806-5813.
Troelstra C, Odijk H, De Wit J, Westerveld A, Thompson LH, Bootsma D et al. Molecular cloning of the human DNA excision repair gene ERCC-6. Molecular and Cellular Biology. 1990;10(11):5806-5813.
Troelstra, C. ; Odijk, H. ; De Wit, J. ; Westerveld, A. ; Thompson, L. H. ; Bootsma, D. ; Hoeijmakers, J. H J. / Molecular cloning of the human DNA excision repair gene ERCC-6. In: Molecular and Cellular Biology. 1990 ; Vol. 10, No. 11. pp. 5806-5813.
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