Journal
MOLECULAR CELL
Volume 8, Issue 2, Pages 407-415Publisher
CELL PRESS
DOI: 10.1016/S1097-2765(01)00319-7
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Funding
- NIGMS NIH HHS [GM19261] Funding Source: Medline
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In both yeast and humans, DNA polymerase (Pol) eta functions in error-free replication of ultraviolet-damaged DNA, and Pol eta promotes replication through many other DNA lesions as well. Here, we present evidence for the physical and functional interaction of yeast Pol eta with proliferating cell nuclear antigen (PCNA) and show that the interaction with PCNA is essential for the in vivo function of Pol eta. Pol eta is highly inefficient at inserting a nucleotide opposite an abasic site, but interaction with PCNA greatly stimulates its ability for nucleotide incorporation opposite this lesion. Thus, in addition to having a pivotal role in the targeting of Pol eta to the replication machinery stalled at DNA lesions, interaction with PCNA would promote the bypass of certain DNA lesions.
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