Affiliation:
1. Department of Biology, Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, North Carolina 27599-3280
Abstract
ABSTRACT
Yeast strains with a mutation in the
MEC1
gene are deficient in the cellular checkpoint response to DNA-damaging agents and have short telomeres (K. B. Ritchie, J. C. Mallory, and T. D. Petes, Mol. Cell. Biol. 19:6065–6075, 1999; T. A. Weinert, G. L. Kiser, and L. H. Hartwell, Genes Dev. 8:652–665, 1994). In wild-type yeast cells, genes inserted near the telomeres are transcriptionally silenced (D. E. Gottschling, O. M. Aparichio, B. L. Billington, and V. A. Zakian, Cell 63:751–762, 1990). We show that
mec1
strains have reduced ability to silence gene expression near the telomere. This deficiency was alleviated by the
sml1
mutation. Overexpression of Mec1p also resulted in a silencing defect, although this overexpression did not affect the checkpoint function of Mec1p. Telomeric silencing was not affected by mutations in several other genes in the Mec1p checkpoint pathway (null mutations in
RAD9
and
CHK1
or in several hypomorphic
rad53
alleles) but was reduced by a null mutation of
DUN1
. In addition, the loss of telomeric silencing in
mec1
strains was not a consequence of the slightly shortened telomeres observed in these strains.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
50 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献