Suppression of cdc13-2-associated senescence by pif1-m2 requires Ku-mediated telomerase recruitment

Author:

Fekete-Szücs Enikő1,Rosas Bringas Fernando R1,Stinus Sonia1ORCID,Chang Michael1ORCID

Affiliation:

1. European Research Institute for the Biology of Ageing, University of Groningen, University Medical Center Groningen, Groningen 9713 AV, The Netherlands

Abstract

Abstract In Saccharomyces cerevisiae, recruitment of telomerase to telomeres requires an interaction between Cdc13, which binds single-stranded telomeric DNA, and the Est1 subunit of telomerase. A second pathway involving an interaction between the yKu complex and telomerase RNA (TLC1) contributes to telomerase recruitment but cannot sufficiently recruit telomerase on its own to prevent replicative senescence when the primary Cdc13-Est1 pathway is abolished—for example, in the cdc13-2 mutant. In this study, we find that mutation of PIF1, which encodes a helicase that inhibits telomerase, suppresses the replicative senescence of cdc13-2 by increasing reliance on the yKu-TLC1 pathway for telomerase recruitment. Our findings reveal new insight into telomerase-mediated telomere maintenance.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology

Reference41 articles.

1. The yeast Pif1p helicase removes telomerase from telomeric DNA;Boulé;Nature,2005

2. Two DNA-binding factors recognize specific sequences at silencers, upstream activating sequences, autonomously replicating sequences, and telomeres in Saccharomyces cerevisiae;Buchman;Mol Cell Biol,1988

3. Two pathways recruit telomerase to Saccharomyces cerevisiae telomeres;Chan;PLoS Genet,2008

4. Structural insights into yeast telomerase recruitment to telomeres;Chen;Cell,2018

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