| Literature DB >> 17218262 |
Wen Hong Shen1, Adayabalam S Balajee, Jianli Wang, Hong Wu, Charis Eng, Pier Paolo Pandolfi, Yuxin Yin.
Abstract
A broad spectrum of mutations in PTEN, encoding a lipid phosphatase that inactivates the P13-K/AKT pathway, is found associated with primary tumors. Some of these mutations occur outside the phosphatase domain, suggesting that additional activities of PTEN function in tumor suppression. We report a nuclear function for PTEN in controlling chromosomal integrity. Disruption of Pten leads to extensive centromere breakage and chromosomal translocations. PTEN was found localized at centromeres and physically associated with CENP-C, an integral component of the kinetochore. C-terminal PTEN mutants disrupt the association of PTEN with centromeres and cause centromeric instability. Furthermore, Pten null cells exhibit spontaneous DNA double-strand breaks (DSBs). We show that PTEN acts on chromatin and regulates expression of Rad51, which reduces the incidence of spontaneous DSBs. Our results demonstrate that PTEN plays a fundamental role in the maintenance of chromosomal stability through the physical interaction with centromeres and control of DNA repair. We propose that PTEN acts as a guardian of genome integrity.Entities:
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Year: 2007 PMID: 17218262 DOI: 10.1016/j.cell.2006.11.042
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582