Repression of RNA polymerase III transcription by the retinoblastoma protein

被引:187
作者
White, RJ
Trouche, D
Martin, K
Jackson, SP
Kouzarides, T
机构
[1] UNIV CAMBRIDGE,DEPT PATHOL,CAMBRIDGE CB2 1QP,ENGLAND
[2] WELLCOME CRC INST,CAMBRIDGE CB2 1QR,ENGLAND
[3] UNIV CAMBRIDGE,DEPT ZOOL,CAMBRIDGE CB2 3EJ,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1038/382088a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
TRANSCRIPTION by RNA polymerase (pol) III is under cell-cycle control, being higher in S and G2 than in G0 and early G1 phases(1-4), Many transformed cell types have elevated pol III activity(4-9), presumably to sustain sufficient protein synthesis for unrestrained growth, The retinoblastoma tumour-suppressor protein (Rb) restricts cellular proliferation, and is often found mutated in transformed cells(10,11). Here we demonstrate that Rb can repress the level of transcription from pol III templates both in vitro and in vivo. Analysis of Rb-deficient SAOS2 cells and primary fibroblasts from Rb--/- mice demonstrates elevated levels of pol III activity in the abscence of functional Rb protein, Rb-induced repression of pol III activity is alleviated by mutations in the Rb pocket domain that occur naturally in tumours, and by viral transforming proteins that hind and inactivate Rb, These results implicate repression of pol III transcription as a mechanism for Rb-induced growth arrest, and suggest that restraining protein biosynthesis may be important in the prevention of tumour development.
引用
收藏
页码:88 / 90
页数:3
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