Regulation of CDK4 activity by a novel CDK4-binding protein, p34SEI-1

被引:96
作者
Sugimoto, M
Nakamura, T
Ohtani, N
Hampson, L
Hampson, IN
Shimamoto, A
Furuichi, Y
Okumura, K
Niwa, S
Taya, Y
Hara, E [1 ]
机构
[1] Christie Hosp NHS Trust, Paterson Inst Canc Res, Manchester M20 4BX, Lancs, England
[2] Juntendo Univ, Sch Med, Tokyo 113, Japan
[3] Sumitomo Elect Ind Ltd, Yokohama, Kanagawa, Japan
[4] St Marys Hosp, Manchester M13 0JH, Lancs, England
[5] Agene Res Inst, Kamakura, Kanagawa, Japan
[6] Natl Canc Ctr, Res Inst, Tokyo 104, Japan
关键词
cyclin D1; CDK4; p16(INK4a);
D O I
10.1101/gad.13.22.3027
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The p16(INK4a) tumor suppressor inhibits cyclin-dependent kinases (CDK4 and CDK6). Here we report the isolation of a novel gene, SEI-1, whose product (p34(SEI-1)) appears to antagonize the function of p16(INK4a). Addition of p34(SEI-1) to cyclin D1-CDK4 renders the complex resistant to inhibition by p16(INK4a). Expression of SEI-1 is rapidly induced on addition of serum to quiescent fibroblasts, and ectopic expression of p34(SEI-1) enables fibroblasts to proliferate even in low serum concentrations. p34(SEI-1) seems to act as a growth factor sensor and may facilitate the formation and activation of cyclin D-CDK complexes in the face of inhibitory levels of INK4 proteins.
引用
收藏
页码:3027 / 3033
页数:7
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