@article{91051,
  keywords = {Gene Deletion, DNA-Binding Proteins, Cell Cycle Proteins, Saccharomyces cerevisiae Proteins, Protein-Serine-Threonine Kinases, Saccharomyces cerevisiae, Intracellular Signaling Peptides and Proteins, Telomere, Exodeoxyribonucleases, Telomerase, Telomere-Binding Proteins, Endodeoxyribonucleases},
  author = {Lara Goudsouzian and Creighton Tuzon and Virginia Zakian},
  title = {S. cerevisiae Tel1p and Mre11p are required for normal levels of Est1p and Est2p telomere association.},
  abstract = { In diverse organisms, the Mre11 complex and phosphoinositide 3-kinase-related kinases (PIKKs), such as Tel1p and Mec1p from S. cerevisiae, are key mediators of DNA repair and DNA damage checkpoints that also function at telomeres. Here, we use chromatin immunoprecipitation (ChIP) to determine if Mre11p, Tel1p, or Mec1p affects telomere maintenance by promoting recruitment of telomerase subunits to S. cerevisiae telomeres. We find that recruitment of Est2p, the catalytic subunit of telomerase, and Est1p, a telomerase accessory protein, was severely reduced in mre11Delta and tel1Delta cells. In contrast, the levels of Est2p and Est1p binding in late S/G2 phase, the period in the cell cycle when yeast telomerase lengthens telomeres, were indistinguishable in wild-type (WT) and mec1Delta cells. These data argue that Mre11p and Tel1p affect telomere length by promoting telomerase recruitment to telomeres, whereas Mec1p has only a minor role in telomerase recruitment in a TEL1 cell. },
  year = {2006},
  journal = {Mol Cell},
  volume = {24},
  pages = {603-10},
  month = {11/2006},
  issn = {1097-2765},
  doi = {10.1016/j.molcel.2006.10.005},
  language = {eng},
}