Tissier, A., Kannouche, P., Reck, M.- P., Lehmann, A. R., Fuchs, R. P. P. and Cordonnier, A. (2004) Co-localization in replication foci and interaction of human Y-family members, DNA polymerase polh and Rev1 protein. DNA Repair, 4 (3). pp. 1503-1514. ISSN 1568-7864Full text not available from this repository.
The progress of replicative DNA polymerases along the replication fork may be impeded by the presence of lesions in the genome. One way to circumvent such hurdles involves the recruitment of specialized DNA polymerases that perform limited incorporation of nucleotides in the vicinity of the damaged site. This process entails DNA polymerase switch between replicative and specialized DNA polymerases. Five eukaryotic proteins can carry out translesion synthesis (TLS) of damaged DNA in vitro, DNA polymerases ζ, η, ι, and κ, and REV1. To identify novel proteins that interact with hpolη, we performed a yeast two-hybrid screen. In this paper, we show that hREV1 interacts with hpolη as well as with hpolκ and poorly with hpolι. Furthermore, cellular localization analysis demonstrates that hREV1 is present, with hpolη in replication factories at stalled replication forks and is tightly associated with nuclear structures. This hREV1 nuclear localization occurs independently of the presence of hpolη. Taken together, our data suggest a central role for hREV1 as a scaffold that recruits DNA polymerases involved in TLS.
|Subjects:||?? QH426 ??|
|Depositing User:||Gee Wheatley|
|Date Deposited:||05 Oct 2007|
|Last Modified:||13 Jun 2012 14:05|
|Google Scholar:||117 Citations|