Nucleic Acids Research, Vol 27, Issue 22 4468-4475, Copyright © 1999 by Oxford University Press
W Lin, H Xin, Y Zhang, X Wu, F Yuan and Z Wang
DNA is frequently damaged by various physical and chemical agents. DNA
damage can lead to mutations during replication. In the yeast Saccharomyces
cerevisiae, the damage-induced mutagenesis pathway requires the Rev1
protein. We have isolated a human cDNA homologous to the yeast REV1 gene.
The human REV1 cDNA consists of 4255 bp and codes for a protein of 1251
amino acid residues with a calculated molecular weight of 138 248 Da. The
human REV1 gene is localized between 2q11.1 and 2q11.2. We show that the
human REV1 protein is a dCMP transferase that specifically inserts a dCMP
residue opposite a DNA template G. In addition, the human REV1 transferase
is able to efficiently and specifically insert a dCMP opposite a DNA
template apurinic/apyrimidinic (AP) site or a uracil residue. These results
suggest that the REV1 transferase may play a critical role during mutagenic
translesion DNA synthesis bypassing a template AP site in human cells.
Consistent with its role as a fundamental mutagenic protein, the REV1 gene
is ubiquitously expressed in various human tissues.
ARTICLES
The human REV1 gene codes for a DNA template-dependent dCMP transferase
Graduate Center for Toxicology, University of Kentucky, Lexington, KY 40536, USA.
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