An alternative pathway for gene regulation by Myc

被引:289
作者
Peukert, K
Staller, P
Schneider, A
Carmichael, G
Hanel, F
Eilers, M
机构
[1] HANS KNOLL INST NAT STOFF FORSCH,DEPT CELL & MOL BIOL,D-07745 JENA,GERMANY
[2] ZENTRUM MOL BIOL,D-69120 HEIDELBERG,GERMANY
[3] UNIV CONNECTICUT,CTR HLTH,DEPT MICROBIOL,FARMINGTON,CT 06030
关键词
gene repression; Miz-1; Myc; POZ domain;
D O I
10.1093/emboj/16.18.5672
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 c-Myc protein activates transcription as part of a heteromeric complex with Max, However, Myc-transformed cells are characterized by loss of expression of several genes, suggesting that Myc may also repress gene expression, Two-hybrid cloning identifies a novel POZ domain Zn finger protein (Mit-1; Myc-interacting Zn finger protein-1) that specifically interacts with Myc, but not with Max or USF. Miz-1 binds to start sites of the adenovirus major late and cyclin D1 promoters and activates transcription from both promoters. Miz-1 has a potent growth arrest function, Binding of Myc to Miz-1 requires the helix-loop-helix domain of Myc and a short amphipathic helix located in the carboxy-terminus of Miz-1, Expression of Myc inhibits transactivation, overcomes Miz-1-induced growth arrest and renders Miz-1 insoluble in vivo, These processes depend on Myc and Miz-1 association and on the integrity of the POZ domain of Miz-1, suggesting that Myc binding activates a latent inhibitory function of this domain, Fusion of a nuclear localization signal induces efficient nuclear transport of Miz-1 and impairs the ability of Myc to overcome transcriptional activation and growth arrest by Miz-1. Our data suggest a model for how gene repression by Myc may occur in vivo.
引用
收藏
页码:5672 / 5686
页数:15
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