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PMID: 10753775 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Sloppier copier DNA polymerases involved in genome repair.

Current opinion in genetics & development ·Vol. 10 ·No. 2 ·2000-04-00 ·Pages 162-8

Goodman MF, Tippin B

Abstract

When chromosomal replication is impeded in the presence of DNA damage, members of a newly discovered UmuC/DinB/Rev1/Rad30 superfamily of procaryotic and eucaryotic DNA polymerases catalyze translesion synthesis at blocked replication forks. Although these polymerases share sequence elements essentially unrelated to the standard replication and repair enzymes, some of them (such as the SOS-induced Escherichia coli pol V) catalyze 'error-prone' translesion synthesis leading to large increases in mutation, whereas others (an example being the Xeroderma pigmentosum variant gene product XPV pol eta) carry out aberrant, yet nonmutagenic translesion synthesis. Ongoing studies of these low fidelity polymerases could provide new insights into the mechanism of somatic hypermutation, a key element in the immune response.

MeSH Terms
Animals DNA Repair/genetics DNA-Directed DNA Polymerase/genetics Escherichia coli/genetics Escherichia coli Proteins Genome, Bacterial Humans Multigene Family Mutagenesis SOS Response, Genetics/genetics
Chemicals
Escherichia coli Proteins DNA polymerase V, E coli DNA-Directed DNA Polymerase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Goodman M F
Department of Biological Sciences and Chemistry, University of Southern California, Los Angeles, 90089-1340, USA. mgoodman@mizar. usc.edu
Tippin B
Article Info
Journal
Current opinion in genetics & development
Abbr.
Curr Opin Genet Dev
ISSN
0959-437X
Published
2000-04-00
Pages
162-8
Language
English
Region
England
NLM ID
9111375
Subset
IM
Grants
NIA NIH HHS · AG00093 · United States
NIGMS NIH HHS · GM21422 · United States
NIGMS NIH HHS · GM42554 · United States
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