Telomere Protection by TPP1/POT1 Requires Tethering to TIN2

被引:192
作者
Takai, Kaori K. [1 ]
Kibe, Tatsuya [1 ]
Donigian, Jill R. [1 ]
Frescas, David [1 ]
de Lange, Titia [1 ]
机构
[1] Rockefeller Univ, Cell Biol & Genet Lab, New York, NY 10065 USA
基金
日本学术振兴会;
关键词
REPLICATION PROTEIN-A; SINGLE-STRANDED-DNA; ABERRANT HOMOLOGOUS RECOMBINATION; DYSKERATOSIS-CONGENITA; MAMMALIAN TELOMERES; HUMAN POT1; CHECKPOINT ACTIVATION; LENGTH REGULATOR; HUMAN-CELLS; COMPLEX;
D O I
10.1016/j.molcel.2011.08.043
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
To prevent ATR activation, telomeres deploy the single-stranded DNA binding activity of TPP1/POT1a. POT1a blocks the binding of RPA to telomeres, suggesting that ATR is repressed through RPA exclusion. However, comparison of the DNA binding affinities and abundance of TPP1/POT1a and RPA indicates that TPP1/POT1a by itself is unlikely to exclude RPA. We therefore analyzed the central shelterin protein TIN2, which links TPP1/POT1a (and POT1b) to TRF1 and TRF2 on the double-stranded telomeric DNA. Upon TIN2 deletion, telomeres lost TPP1/POT1a, accumulated RPA, elicited an ATR signal, and showed all other phenotypes of POT1a/b deletion. TIN2 also affected the TRF2-dependent repression of ATM kinase signaling but not to TRF2-mediated inhibition of telomere fusions. Thus, while TIN2 has a minor contribution to the repression of ATM by TRF2, its major role is to stabilize TPR1/POT1a on the ss telomeric DNA, thereby allowing effective exclusion of RPA and repression of ATR signaling.
引用
收藏
页码:647 / 659
页数:13
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