| Literature DB >> 22354040 |
Pierre Luciano1, Stéphane Coulon, Virginie Faure, Yves Corda, Julia Bos, Steven J Brill, Eric Gilson, Marie-Noelle Simon, Vincent Géli.
Abstract
In Saccharomyces cerevisiae, the telomerase complex binds to chromosome ends and is activated in late S-phase through a process coupled to the progression of the replication fork. Here, we show that the single-stranded DNA-binding protein RPA (replication protein A) binds to the two daughter telomeres during telomere replication but only its binding to the leading-strand telomere depends on the Mre11/Rad50/Xrs2 (MRX) complex. We further demonstrate that RPA specifically co-precipitates with yKu, Cdc13 and telomerase. The interaction of RPA with telomerase appears to be mediated by both yKu and the telomerase subunit Est1. Moreover, a mutation in Rfa1 that affects both the interaction with yKu and telomerase reduces the dramatic increase in telomere length of a rif1Δ, rif2Δ double mutant. Finally, we show that the RPA/telomerase association and function are conserved in Schizosaccharomyces pombe. Our results indicate that in both yeasts, RPA directly facilitates telomerase activity at chromosome ends.Entities:
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Year: 2012 PMID: 22354040 PMCID: PMC3343328 DOI: 10.1038/emboj.2012.40
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598