The roles of PCNA SUMOylation, Mms2-Ubc13 and Rad5 in translesion DNA synthesis in Saccharomyces cerevisiae
Author:
Publisher
Wiley
Subject
Molecular Biology,Microbiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2958.2011.07610.x/fullpdf
Reference46 articles.
1. Regulation of alternative replication bypass pathways at stalled replication forks and its effects on genome stability: a yeast model;Barbour;Mutat Res,2003
2. Ubiquitin-binding domains in Y-family polymerases regulate translesion synthesis;Bienko;Science,2005
3. Yeast Rad5 protein required for postreplication repair has a DNA helicase activity specific for replication fork regression;Blastyak;Mol Cell,2007
4. Suppression of genetic defects within RAD6 pathway by srs2 is specific for error-free post-replication repair but not for damage induced mutagenesis;Broomfield;Nucleic Acid Res,2002
5. MMS2, encoding a ubiquitin-conjugating-enzyme-like protein, is a member of the yeast error-free postreplication repair pathway;Broomfield;Proc Natl Acad Sci USA,1998
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