p53 Suppresses c-Myb-induced trans-Activation and Transformation by Recruiting the Corepressor mSin3A


Autoria(s): Tanikawa, Jun; Nomura, Teruaki; Macmillan, Elizabeth M.; Shinagawa, Toshie; Jin, Wanzhu; Kokura, Kenji; Baba, Daichi; Shirakawa, Masahiro; Gonda, Thomas J.; Ishii, Shunsuke
Data(s)

01/01/2004

Resumo

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.

Identificador

http://espace.library.uq.edu.au/view/UQ:42099

Idioma(s)

eng

Publicador

Amer Soc Biochemistry Molecular Biology Inc

Palavras-Chave #Biochemistry & Molecular Biology #Dna-binding Domain #Transcriptional Activation #Hematopoietic-cells #V-myb #Negative Regulation #Functional Domain #Tumor Suppression #Expression #Gene #Apoptosis #320000 Medical and Health Sciences
Tipo

Journal Article