Pot1 deficiency initiates DNA damage checkpoint activation and aberrant homologous recombination at telomeres - PubMed (original) (raw)
. 2006 Jul 14;126(1):49-62.
doi: 10.1016/j.cell.2006.05.037.
Asha S Multani, Hua He, Wilfredo Cosme-Blanco, Yu Deng, Jian Min Deng, Olga Bachilo, Sen Pathak, Hedioshi Tahara, Susan M Bailey, Yibin Deng, Richard R Behringer, Sandy Chang
Affiliations
- PMID: 16839876
- DOI: 10.1016/j.cell.2006.05.037
Free article
Pot1 deficiency initiates DNA damage checkpoint activation and aberrant homologous recombination at telomeres
Ling Wu et al. Cell. 2006.
Free article
Abstract
The terminal t-loop structure adopted by mammalian telomeres is thought to prevent telomeres from being recognized as double-stranded DNA breaks by sequestering the 3' single-stranded G-rich overhang from exposure to the DNA damage machinery. The POT1 (protection of telomeres) protein binds the single-stranded overhang and is required for both chromosomal end protection and telomere length regulation. The mouse genome contains two POT1 orthologs, Pot1a and Pot1b. Here we show that conditional deletion of Pot1a elicits a DNA damage response at telomeres, resulting in p53-dependent replicative senescence. Pot1a-deficient cells exhibit overall telomere length and 3' overhang elongation as well as aberrant homologous recombination (HR) at telomeres, manifested as increased telomere sister chromatid exchanges and formation of telomere circles. Telomeric HR following Pot1a loss requires NBS1. Pot1a deletion also results in chromosomal instability. Our results suggest that POT1a is crucial for the maintenance of both telomere integrity and overall genomic stability.
Comment in
- Are mouse telomeres going to pot?
Baumann P. Baumann P. Cell. 2006 Jul 14;126(1):33-6. doi: 10.1016/j.cell.2006.06.027. Cell. 2006. PMID: 16839874 Review.
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