The suppression of MAD1 by Akt-mediated phosphorylation activates MAD1 target genes transcription.

ASIA unversity > 醫學暨健康學院 > 生物科技學系 > 期刊論文 > Item 310904400/16136

請使用永久網址來引用或連結此文件: http://asiair.asia.edu.tw/ir/handle/310904400/16136

題名:	The suppression of MAD1 by Akt-mediated phosphorylation activates MAD1 target genes transcription.
作者:	;Chou, C-K.;Lee, D-F;Sun, H-L;李龍緣;Li, Long-Yuan;Lin, C-Y;黃偉謙;Huang, W-C;Hsu, J-M;Kuo, H-P;Yamaguchi, H;Wang, Y-N;Liu, M;Wu, H-Y;Liao, P-C;Yen, C-J;洪明奇;Hung, Mien-Chie
貢獻者:	生物科技學系
關鍵詞:	AKT;MAD1;hTERT
日期:	2009
上傳時間:	2012-11-23 09:09:01 (UTC+0)
摘要:	MAX dimerization protein 1 (MAD1) is a transcription suppressor that antagonizes MYC-mediated transcription activation, and the inhibition mechanism occurs mainly through the competition of target genes' promoter MYC binding sites by MAD1. The promoter binding proteins switch between MYC and MAD1 affects cell proliferation and differentiation. However, little is known about MAD1's regulation process in cancer cells. Here, we present evidence that AKT inhibits MAD1-mediated transcription repression by physical interaction with and phosphorylation of MAD1. Phosphorylation reduces the binding affinity between MAD1 and its target genes' promoter and thereby abolishes its transcription suppression function. Mutation of the phosphorylation site from serine to alanine rescues the DNA-binding ability in the presence of activated AKT. In addition, AKT inhibits MAD1 mediated target genes (hTERT and ODC) transcription repression and promotes cell cycle and cell growth. However, mutated S145A MAD1 abrogates the inhibition by AKT. Thus, our results suggest that phosphorylation of MAD1 by AKT inhibits MAD1-mediated transcription suppression and subsequently activates the transcription of MAD1 target genes
關聯:	MOLECULAR CARCINOGENESIS
顯示於類別:	[生物科技學系] 期刊論文

文件中的檔案:

檔案	描述	大小	格式	瀏覽次數
index.html		0Kb	HTML	494	檢視/開啟

在ASIAIR中所有的資料項目都受到原著作權保護.

資料載入中.....