Subtelomeric factors antagonize telomere anchoring and Tel1-independent telomere length regulation

被引:37
作者
Hediger, F
Berthiau, AS
van Houwe, G
Gilson, E
Gasser, SM
机构
[1] Friedrich Miescher Inst Biomed Res, CH-4058 Basel, Switzerland
[2] Ecole Normale Super Lyon, CNRS, UMR5161, Mol Biol Lab, F-69364 Lyon, France
[3] Univ Geneva, Dept Mol Biol, CH-1211 Geneva, Switzerland
[4] Univ Geneva, NCCR Frontiers Genet, CH-1211 Geneva, Switzerland
关键词
nuclear organization; Sir4; telomerase; telomeres; yKu;
D O I
10.1038/sj.emboj.7600976
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Yeast telomeres are anchored at the nuclear envelope ( NE) through redundant pathways that require the telomerebinding factors yKu and Sir4. Significant variation is observed in the efficiency with which different telomeres are anchored, however, suggesting that other forces influence this interaction. Here, we show that subtelomeric elements and the insulator factors that bind them antagonize the association of telomeres with the NE. This is detectable when the redundancy in anchoring pathways is compromised. Remarkably, these same conditions lead to a reduction in steady- state telomere length in the absence of the ATM- kinase homologue Tel1. Both the delocalization of telomeres and reduction in telomere length can be induced by targeting of Tbf1 or Reb1, or the viral transactivator VP16, to a site 23 kb away from the TG repeat. This correlation suggests that telomere anchoring and a Tel1-independent pathway of telomere length regulation are linked, lending a functional significance to the association of yeast telomeres with the NE.
引用
收藏
页码:857 / 867
页数:11
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