Telomere protection by mammalian Pot1 requires interaction with Tpp1

被引:0
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作者
Dirk Hockemeyer
Wilhelm Palm
Tobias Else
Jan-Peter Daniels
Kaori K Takai
Jeffrey Z-S Ye
Catherine E Keegan
Titia de Lange
Gary D Hammer
机构
[1] Laboratory for Cell Biology and Genetics,Department of Internal Medicine, Division of Metabolism
[2] The Rockefeller University,Division of Hematology
[3] Endocrinology and Diabetes,Department of Pediatrics, Division of Genetics
[4] University of Michigan Health System,undefined
[5] 109 Zina Pitcher Pl.,undefined
[6] New York University School of Medicine,undefined
[7] University of Michigan,undefined
[8] Current addresses: Sir William Dunn School of Pathology,undefined
[9] University of Oxford,undefined
[10] South Parks Road,undefined
[11] OX1 3RE Oxford,undefined
[12] UK (J.-P.D.) and Department of Oncology,undefined
[13] Kaiser Permanente Medical Group,undefined
[14] Santa Rosa,undefined
[15] California 95403,undefined
[16] USA (J.Z.-S.Y.).,undefined
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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.
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页码:754 / 761
页数:7
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