Telomere protection by mammalian Pot1 requires interaction with Tpp1

被引:149
作者
Hockemeyer, Dirk
Palm, Wilhelm
Else, Tobias
Daniels, Jan-Peter
Takai, Kaori K.
Ye, Jeffrey Z-S
Keegan, Catherine E.
de Lange, Titia
Hammer, Gary D.
机构
[1] Rockefeller Univ, Lab Cell Biol & Genet, New York, NY 10065 USA
[2] Univ Michigan Hlth Syst, Dept Internal Med, Div Metab Endocrinol & Diabet, Ann Arbor, MI 48109 USA
[3] NYU, Sch Med, Div Hematol, New York, NY 10016 USA
[4] Univ Michigan, Div Genet, Dept Pediat, Ann Arbor, MI 48109 USA
关键词
D O I
10.1038/nsmb1270
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
The shelterin complex at mammalian telomeres contains the single-stranded DNA-binding protein Pot1, which regulates telomere length and protects chromosome ends. Pot1 binds Tpp1, the shelterin component that connects Pot1 to the duplex telomeric DNA-binding proteins Trf1 and Trf2. Control of telomere length requires that Pot1 binds Tpp1 as well as the single-stranded telomeric DNA, but it is not known whether the protective function of Pot1 depends on Tpp1. Alternatively, Pot1 might function similarly to the Pot1-like proteins of budding and fission yeast, which have no known Tpp1-like connection to the duplex telomeric DNA. Using mutant mouse cells with diminished Tpp1 levels, RNA interference directed to mouse Tpp1 and Pot1, and complementation of mouse Pot1 knockout cells with human and mouse Pot1 variants, we show here that Tpp1 is required for the protective function of mammalian Pot1 proteins.
引用
收藏
页码:754 / 761
页数:8
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