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Evolution and mutagenesis of the mammalian excision repair geneERCC-1
Author(s) -
M. van Duin,
Jacolien van den Tol,
P A Warmerdam,
Hanny Odijk,
Dies Meijer,
A. Westerveld,
D. Bootsma,
Jan H.J. Hoeijmakers
Publication year - 1988
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/16.12.5305
Subject(s) - biology , dna repair , nucleotide excision repair , gene , mutagenesis , homology (biology) , saccharomyces cerevisiae , genetics , dna , conserved sequence , microbiology and biotechnology , peptide sequence , mutation
The human DNA excision repair protein ERCC-1 exhibits homology to the yeast RAD10 repair protein and its longer C-terminus displays similarity to parts of the E. coli repair proteins uvrA and uvrC. To study the evolution of this 'mosaic' ERCC-1 gene we have isolated the mouse homologue. Mouse ERCC-1 harbors the same pattern of homology with RAD10 and has a comparable C-terminal extension as its human equivalent. Mutation studies show that the strongly conserved C-terminus is essential in contrast to the less conserved N-terminus which is even dispensible. The mouse ERCC-1 amino acid sequence is compatible with a previously postulated nuclear location signal and DNA-binding domain. The ERCC-1 promoter harbors a region which is highly conserved in mouse and man. Since the ERCC-1 promoter is devoid of all classical promoter elements this region may be responsible for the low constitutive level of expression in all mouse tissues and stages of embryogenesis examined.

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