| Literature DB >> 2184031 |
C A Weber1, E P Salazar, S A Stewart, L H Thompson.
Abstract
Human ERCC2 genomic clones give efficient, stable correction of the nucleotide excision repair defect in UV5 Chinese hamster ovary cells. One clone having a breakpoint just 5' of classical promoter elements corrects only transiently, implicating further flanking sequences in stable gene expression. The nucleotide sequences of a cDNA clone and genomic flanking regions were determined. The ERCC2 translated amino acid sequence has 52% identity (73% homology) with the yeast nucleotide excision repair protein RAD3. RAD3 is essential for cell viability and encodes a protein that is a single-stranded DNA dependent ATPase and an ATP dependent helicase. The similarity of ERCC2 and RAD3 suggests a role for ERCC2 in both cell viability and DNA repair and provides the first insight into the biochemical function of a mammalian nucleotide excision repair gene.Entities:
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Year: 1990 PMID: 2184031 PMCID: PMC551832 DOI: 10.1002/j.1460-2075.1990.tb08260.x
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598