Human TAF(parallel to)105 is a cell type-specific TFIID subunit related to hTAF(parallel to)130

被引:151
作者
Dikstein, R
Zhou, S
Tjian, R
机构
[1] Howard Hughes Medical Institute, Dept. of Molecular and Cell Biology, University of California, Berkeley
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0092-8674(00)81330-6
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
We previously characterized Drosophila and human TAF subunits that make up the core TFIID complex found in all cells. Here, we report that differentiated B cells contain a novel substoichiometric TAF of 105 kDa not found associated with TFIID isolated from other cell types. The cDNA encoding hTAF(II)105 reveals a highly conserved C-terminal domain shared by hTAF(II)130 and dTAF(II)110, while the N-terminal coactivator domain has diverged significantly. All cells tested express TAF(II)105 mRNA, but only B cells contain significant levels of protein associated with TFIID. Transient overexpression of hTAF(II)105 selectively squelches the transcription of some genes in B cells. These properties suggest that TAF(II)105 is a cell type-specific subunit of TFIID that may be responsible for mediating transcription by a subset of activators in B cells.
引用
收藏
页码:137 / 146
页数:10
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