Two MAD tails:: what the recent knockouts of Madl and Mxil tell us about the MYC/MAX/MAD network

被引:45
作者
Foley, KP [1 ]
Eisenman, RN [1 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 1999年 / 1423卷 / 03期
关键词
cancer; knockout mouse; MAD; MAX; MYC; targeted gene disruption; transcriptional repression; tumorigenesis; tumor suppressor;
D O I
10.1016/S0304-419X(99)00012-8
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
Members of the MAD/MXI protein family heterodimerize with MAX and repress transcription by recruiting a chromatin-modifying co-repressor complex to specific DNA target genes. Repression mediated by MAD is thought to antagonize the transcriptional activation and proliferation-promoting functions of MYC-MAX heterodimers. Because they are induced during differentiation, it has been suggested that MAD proteins act to limit cell proliferation during terminal differentiation. There is also controversial evidence that these proteins may function as tumor suppressors. Recently, targeted gene deletions of two members of this gene family, Mad1 and Mxi1, have been carried out in mice. Although these animals display what appear to be quite different phenotypes, further analysis supports the view that both these proteins function in cell-cycle exit during terminal differentiation, and that at least MXI1 can act as a tumor suppressor. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:M37 / M47
页数:11
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