Cdk phosphorylation triggers sequential intramolecular interactions that progressively block Rb functions as cells move through G1

被引:850
作者
Harbour, JW
Luo, RX
Santi, AD
Postigo, AA
Dean, DC [1 ]
机构
[1] Washington Univ, Sch Med, Dept Med, Div Mol Oncol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Ophthalmol & Visual Sci, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0092-8674(00)81519-6
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
We present evidence that phosphorylation of the C-terminal region of Rb by Cdk4/6 initiates successive intramolecular interactions between the C-terminal region and the central pocket. The initial interaction displaces histone deacetylase from the pocket, blocking active transcriptional repression by Rb. This facilitates a second interaction that leads to phosphorylation of the pocket by Cdk2 and disruption of pocket structure. These intramolecular interactions provide a molecular basis for sequential phosphorylation of Rb by Cdk4/6 and Cdk2. Cdk4/6 is activated early in G1, blocking active repression by Rb. However, it is not until near the end of G1, when cyclin E is expressed and Cdk2 is activated, that Rb is prevented from binding and inactivating E2F.
引用
收藏
页码:859 / 869
页数:11
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