Sp1-mediated transcription regulation of TAF-Iα gene encoding a histone chaperone

被引:20
作者
Asaka, Masamitsu N.
Murano, Kensaku
Nagata, Kyosuke [1 ]
机构
[1] Univ Tsukuba, Dept Infect Biol, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki 3058575, Japan
关键词
Adenovirus; Chromatin remodeling; SET; TAF-I; Transcription factor;
D O I
10.1016/j.bbrc.2008.09.053
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
TAF-I, one of histone chaperones, consists of two subtypes, TAF-I alpha and TAF-I beta. The histone chaperone activity of TAF-I is regulated by dimer patterns of these subtypes. TAF-I beta is expressed ubiquitously, while the expression level of TAF-I alpha with less activity than TAF-I beta differs among cell types. It is, therefore, assumed that the expression level of TAF-I alpha in a cell is important for the TAF-I activity level. Here, we found that TAF-I alpha and TAF-I beta genes are under the control of distinct promoters. Reporter assays and gel shift assays demonstrated that Sp1 binds to three regions in the TAF-I alpha promoter and two or all mutaions of the three Sp1 binding regions reduced the TAF-I alpha promoter activity. ChIP assays demonstrated that Sp1 binds to the TAF-I alpha promoter in vivo. Furthermore, the expression level of TAF-I alpha mRNA was reduced by knockdown of Sp1 using siRNA method. These studies indicated that the TAF-I alpha promoter is under the control of Sp1. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:665 / 670
页数:6
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