MBP-1 physically associates with histone deacetylase for transcriptional repression

被引:22
作者
Ghosh, AK
Steele, R
Ray, RB
机构
[1] St Louis Univ, Dept Pathol, St Louis, MO 63104 USA
[2] St Louis Univ, Div Infect Dis & Immunol, St Louis, MO 63104 USA
关键词
D O I
10.1006/bbrc.1999.0921
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
MBP-1, a c-myc promoter binding protein, is a mammalian transcription factor with intriguing properties including transcriptional repression of cellular genes. Recently, we have identified and characterized two different repressor domains of MBP-1. In this report, we have demonstrated that MBP-1 physically associates with histone deacetylase (HDAC), thus promoting formation of neucleosomes that inhibit transcription. Trichostatin A, an inhibitor of histone deacetylase, significantly reduces MBP-1-mediated transcriptional repression. However, MBP-1-mediated repression on c-myc promoter is resistant to histone deacetylase activity. Our results suggest that MBP-1 represses transcription by recruiting histone deacetylase as one of the mechanisms, whereas the other mechanism is resistant to HDAC activity and probably related to direct binding of promoter sequences or interaction through yet unidentified factor, (C) 1999 Academic Press.
引用
收藏
页码:405 / 409
页数:5
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