Tel1p preferentially associates with short telomeres to stimulate their elongation

被引:109
作者
Hector, Ronald E.
Shtofman, Rebecca L.
Ray, Alo
Chen, Bo-Ruei
Nyun, Thihan
Berkner, Kathleen L.
Runge, Kurt W.
机构
[1] Case Western Reserve Univ, Cleveland Clin Lerner Coll Med, Dept Mol Genet, Lerner Res Inst, Cleveland, OH 44195 USA
[2] Case Western Reserve Univ, Cleveland Clin Lerner Coll Med, Dept Mol Cardiol, Lerner Res Inst, Cleveland, OH 44195 USA
[3] Case Western Reserve Univ, Sch Med, Dept Genet, Cleveland, OH 44106 USA
关键词
D O I
10.1016/j.molcel.2007.08.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
In many organisms, telomeric DNA consists of long tracts of short repeats. Shorter tracts are preferentially lengthened by telomerase, suggesting a conserved mechanism that recognizes and elongates short telomeres. Tel1p, an ATM family checkpoint kinase, plays an important role in telomere elongation, as cells lacking Tel1p have short telomeres and show reduced recruitment of telomerase components to telomeres. We show that Tel1p association increased as telomeres shortened in vivo in the presence or absence of telomerase and that Tel1p preferentially associated with the shortest telomeres. Tel1p association was independent of Tel1p kinase activity and enhanced by Mre11p. Tel1p overexpression simultaneously stimulated telomerase-mediated elongation and Tel1p association with all telomeres. Thus, Tel1p preferentially associates with the shortest telomeres and stimulates their elongation by telomerase.
引用
收藏
页码:851 / 858
页数:8
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