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Two MAD tails: what the recent knockouts of Mad1 and Mxi1 tell us about the MYC/MAX/MAD network.

Foley, K P and Eisenman, R N (1999) Two MAD tails: what the recent knockouts of Mad1 and Mxi1 tell us about the MYC/MAX/MAD network. Biochimica et biophysica acta, 1423 (3). M37-M47. ISSN 0006-3002

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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.

Item Type: Article or Abstract
DOI: 10.1016/S0304-419X(99)00012-8
PubMed ID: 10382539
Grant Numbers: RO1CA57138, HL54881
Keywords or MeSH Headings: Animals; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors; Basic Helix-Loop-Helix Transcription Factors; Basic-Leucine Zipper Transcription Factors; Cell Differentiation; Cell Division; DNA-Binding Proteins/genetics; Gene Deletion; Genes, Tumor Suppressor; Granulocytes/metabolism; Mice; Mice, Knockout; Repressor Proteins; Trans-Activation (Genetics); Transcription Factors/genetics; Tumor Suppressor Proteins;
Subjects: Molecules > Proteins > Transcription factors
Cellular and Organismal Processes > Cell Physiology > Cell differentiation
Depositing User: Library Staff
Date Deposited: 25 Nov 2008 19:14
Last Modified: 28 Sep 2011 00:32

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