Lysine methylation regulates the pRb tumour suppressor protein

被引:96
作者
Munro, S. [1 ]
Khaire, N. [1 ]
Inche, A. [1 ]
Carr, S. [1 ]
La Thangue, N. B. [1 ]
机构
[1] Univ Oxford, Canc Biol Lab, Dept Clin Pharmacol, Div Med Sci, Oxford OX3 7DQ, England
关键词
tumour suppressor; pRb; lysine methylation; Set7/9; HP1; RETINOBLASTOMA GENE-PRODUCT; CELL-CYCLE CONTROL; TRANSCRIPTION FACTOR; HISTONE METHYLATION; MUSCLE-CELLS; IN-VIVO; DIFFERENTIATION; E2F; ACETYLATION; BINDING;
D O I
10.1038/onc.2009.511
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 pRb tumour suppressor protein has a central role in coordinating early cell cycle progression. An important level of control imposed on pRb occurs through post-translational modi. cation, for example, phosphorylation. We describe here a new level of regulation on pRb, mediated through the targeted methylation of lysine residues, by the methyltransferase Set7/9. Set7/9 methylates the C-terminal region of pRb, both in vitro and in cells, and methylated pRb interacts with heterochromatin protein HP1. pRb methylation is required for pRb-dependent cell cycle arrest and transcriptional repression, as well as pRb-dependent differentiation. Our results indicate that methylation can influence the properties of pRb, and raise the interesting possibility that methylation modulates pRb tumour suppressor activity. Oncogene (2010) 29, 2357-2367; doi:10.1038/onc.2009.511; published online 8 February 2010
引用
收藏
页码:2357 / 2367
页数:11
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