An LXXLL motif in nuclear receptor corepressor mediates ligand-induced repression of the thyroid stimulating hormone-β gene

被引:5
|
作者
Loinder, K [1 ]
Söderström, M [1 ]
机构
[1] Linkoping Univ, Div Cell Biol, Dept Biomed & Surg, S-58185 Linkoping, Sweden
基金
瑞典研究理事会;
关键词
nuclear receptor; transcriptional regulation; repression; corepressor; coactivator; siRNA;
D O I
10.1016/j.jsbmb.2005.06.031
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
Nuclear receptor corepressor (N-CoR) regulates gene expression through interaction with DNA-bound nuclear receptors, recruiting multicomponent repressor complexes to the sites of target genes. We recently reported the presence of an LXXLL motif in N-CoR, and showed that this motif interacts in vitro and in vivo with retinoic acid receptor alpha (RAR alpha) and thyroid hormone receptor beta (TR beta). Transient transfection experiments now suggest that TR beta and N-CoR act synergistically and may both be required for ligand-induced repression from the negative TR response element in the thyroid stimulating hormone-beta (TSH beta) gene promoter. Mutation of the LXXLL motif in N-CoR abolished ligand-induced repression at this response element. Furthermore, in vitro binding of N-CoR to a complex between TR beta and the negative TR response element was strictly ligand-dependent. We conclude that N-CoR and TR beta cooperate in the regulation of the TSH beta gene and that the ligand-dependent repression is mediated by the LXXLL motif in N-CoR. (c) 2005 Published by Elsevier Ltd.
引用
收藏
页码:322 / 327
页数:6
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