Repression of p15INK4b expression by Myc through association with Miz-1

被引:465
作者
Staller, P
Peukert, K
Kiermaier, A
Seoane, J
Lukas, J
Karsunky, H
Möröy, T
Bartek, J
Massagué, J
Hänel, F
Eilers, M
机构
[1] Inst Mol Biol & Tumor Res, D-35033 Marburg, Germany
[2] Mem Sloan Kettering Canc Ctr, Cell Biol Program, New York, NY 10021 USA
[3] Inst Canc Biol, DK-2100 Copenhagen, Denmark
[4] Univ Essen Gesamthsch, Inst Cell Biol, D-45122 Essen, Germany
[5] Hans Knoll Inst Naturstoff Forsch, D-07745 Jena, Germany
关键词
D O I
10.1038/35070076
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Deregulated expression of c-myc can induce cell proliferation in established cell lines and in primary mouse embryonic fibroblasts (MEFs), through a combination of both transcriptional activation and repression by Myc. Here we show that a Myc-associated transcription factor, Miz-1, arrests cells in G1 phase and inhibits cyclin D-associated kinase activity. Miz-1 upregulates expression of the cyclin-dependent kinases (CDK) inhibitor p15(INK4b) by binding to the initiator element of the p15(INK4b) promoter. Myc and Max form a complex with Miz-1 at the p15 initiator and inhibit transcriptional activation by Miz-1. Expression of Myc in primary cells inhibits the accumulation of p15(INK4b) that is associated with cellular senescence; conversely deletion of c-myc in an established cell line activates p15(INK4b) expression. Alleles of c-myc that are unable to bind to Miz-1 fail to inhibit accumulation of p15(INK4b) messenger RNA in primary cells and are, as a consequence, deficient in immortalization.
引用
收藏
页码:392 / 399
页数:8
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