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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-59700

Knobel, P A; Marti, T M (2011). Translesion DNA synthesis in the context of cancer research. Cancer Cell International, 11:39.

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Abstract

ABSTRACT: During cell division, replication of the genomic DNA is performed by high-fidelity DNA polymerases but these error-free enzymes can not synthesize across damaged DNA. Specialized DNA polymerases, so called DNA translesion synthesis polymerases (TLS polymerases), can replicate damaged DNA thereby avoiding replication fork breakdown and subsequent chromosomal instability.We focus on the involvement of mammalian TLS polymerases in DNA damage tolerance mechanisms. In detail, we review the discovery of TLS polymerases and describe the molecular features of all the mammalian TLS polymerases identified so far. We give a short overview of the mechanisms that regulate the selectivity and activity of TLS polymerases. In addition, we summarize the current knowledge how different types of DNA damage, relevant either for the induction or treatment of cancer, are bypassed by TLS polymerases. Finally, we elucidate the relevance of TLS polymerases in the context of cancer therapy.

Item Type:Journal Article, refereed, further contribution
Communities & Collections:04 Faculty of Medicine > University Hospital Zurich > Clinic for Oncology
DDC:610 Medicine & health
Language:English
Date:2011
Deposited On:03 Mar 2012 13:24
Last Modified:30 Nov 2013 16:20
Publisher:BioMed Central
ISSN:1475-2867
Publisher DOI:10.1186/1475-2867-11-39
PubMed ID:22047021
Citations:Web of Science®. Times Cited: 8
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Scopus®. Citation Count: 7

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