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Publication : p53 suppresses c-Myb-induced trans-activation and transformation by recruiting the corepressor mSin3A.

First Author  Tanikawa J Year  2004
Journal  J Biol Chem Volume  279
Issue  53 Pages  55393-400
PubMed ID  15509555 Mgi Jnum  J:95035
Mgi Id  MGI:3522540 Doi  10.1074/jbc.M411658200
Citation  Tanikawa J, et al. (2004) p53 suppresses c-Myb-induced trans-activation and transformation by recruiting the corepressor mSin3A. J Biol Chem 279(53):55393-400
abstractText  p53 is known to repress transcription of a number of genes, but the mechanism of p53 recruitment to these target genes is unknown. The c-myb proto-oncogene product (c-Myb) positively regulates proliferation of immature hematopoietic cells, whereas p53 blocks cell cycle progression. Here, we demonstrate that p53 inhibits c-Myb-induced transcription and transformation by directly binding to c-Myb. The ability of c-Myb to maintain the undifferentiated state of M1 cells was also suppressed by p53. p53 did not affect the ability of c-Myb to bind to DNA but formed a ternary complex with the corepressor mSin3A and c-Myb. Thus, p53 antagonizes c-Myb by recruiting mSin3A to down-regulate specific Myb target genes.
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