| Literature DB >> 2676986 |
A Morrison1, R B Christensen, J Alley, A K Beck, E G Bernstine, J F Lemontt, C W Lawrence.
Abstract
We have cloned the REV3 gene of Saccharomyces cerevisiae by complementation of the rev3 defect in UV-induced mutagenesis. The nucleotide sequence of this gene encodes a predicted protein of Mr 172,956 showing significant sequence similarity to Epstein-Barr virus DNA polymerase and to other members of a class of DNA polymerases including human DNA polymerase alpha and yeast DNA polymerase I. REV3 protein shows less sequence identity, and presumably a more distant evolutionary relationship, to the latter two enzymes than they do to each other. Haploids carrying a complete deletion of REV3 are viable. We suggest that induced mutagenesis in S. cerevisiae depends on a specialized DNA polymerase that is not required for other replicative processes. REV3 is located 2.8 centimorgans from CDC60, on chromosome XVI.Entities:
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Year: 1989 PMID: 2676986 PMCID: PMC210411 DOI: 10.1128/jb.171.10.5659-5667.1989
Source DB: PubMed Journal: J Bacteriol ISSN: 0021-9193 Impact factor: 3.490