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e-Article

Ubc9- and Mms21-mediated sumoylation counteracts recombinogenic events at damaged replication forks
Document Type
Report
Source
Cell. Nov, 2006, Vol. 127 Issue 3, p509, 14 p.
Subject
DNA replication -- Research
DNA repair -- Research
Recombinant proteins -- Structure
Recombinant proteins -- Research
Biological sciences
Language
English
ISSN
0092-8674
Abstract
An attempt is made to propose that Ubc9 and Mms21 act in concert with Sgs1 to resolve the X structures formed during replication. The results have shown that Ubc9- and Mms21-mediated sumoylation functions as a regulatory mechanism, which is different from that of replication checkpoints, to prevent pathological accumulation of cruciform structures at damaged forks.