Your browser doesn't support javascript.
loading
RPA facilitates telomerase activity at chromosome ends in budding and fission yeasts.
Luciano, Pierre; Coulon, Stéphane; Faure, Virginie; Corda, Yves; Bos, Julia; Brill, Steven J; Gilson, Eric; Simon, Marie-Noelle; Géli, Vincent.
Afiliación
  • Luciano P; Marseille Cancer Research Center CRCM, U1068 Inserm, UMR7258 CNRS, Aix-Marseille Univ, Institut Paoli-Calmettes, Marseille, France.
EMBO J ; 31(8): 2034-46, 2012 Apr 18.
Article en En | MEDLINE | ID: mdl-22354040
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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Schizosaccharomyces / Cromosomas / Telómero / Telomerasa / Proteínas de Saccharomyces cerevisiae / Proteína de Replicación A Idioma: En Año: 2012 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Schizosaccharomyces / Cromosomas / Telómero / Telomerasa / Proteínas de Saccharomyces cerevisiae / Proteína de Replicación A Idioma: En Año: 2012 Tipo del documento: Article