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Cdc13 cooperates with the yeast Ku proteins and Stn1 to regulate telomerase recruitment.

The Saccharomyces cerevisiae CDC13 protein binds single-strand telomeric DNA. Here we report the isolation of new mutant alleles of CDC13 that confer either abnormal telomere lengthening or telomere shortening. This deregulation not only depended on telomerase (Est2/TLC1) and Est1, a direct regulator of telomerase, but also on the yeast Ku proteins, yKu70/Hdf1 and yKu80/Hdf2, that have been previously implicated in DNA repair and telomere maintenance. Expression of a Cdc13-yKu70 fusion protein resulted in telomere elongation, similar to that produced by a Cdc13-Est1 fusion, thus suggesting that yKu70 might promote Cdc13-mediated telomerase recruitment. We also demonstrate that Stn1 is an inhibitor of telomerase recruitment by Cdc13, based both on STN1 overexpression and Cdc13-Stn1 fusion experiments. We propose that accurate regulation of telomerase recruitment by Cdc13 results from a coordinated balance between positive control by yKu70 and negative control by Stn1. Our results represent the first evidence of a direct control of the telomerase-loading function of Cdc13 by a double-strand telomeric DNA-binding complex.

Pubmed ID: 11046137


  • Grandin N
  • Damon C
  • Charbonneau M


Molecular and cellular biology

Publication Data

November 19, 2000

Associated Grants


Mesh Terms

  • Antigens, Nuclear
  • Chromosomal Proteins, Non-Histone
  • Cyclin B
  • DNA Helicases
  • DNA-Binding Proteins
  • Fungal Proteins
  • Gene Expression Regulation, Fungal
  • Intracellular Signaling Peptides and Proteins
  • Mutation
  • Nuclear Proteins
  • Protein-Serine-Threonine Kinases
  • Recombinant Fusion Proteins
  • Saccharomyces cerevisiae
  • Saccharomyces cerevisiae Proteins
  • Sequence Analysis, DNA
  • Telomerase