Negative regulation of the rat Na-K-ATPase alpha(3)-subunit gene promoter by thyroid hormone

被引:11
作者
He, HP
Chin, S
Zhuang, K
Ron, H
Apriletti, J
Gick, G
机构
[1] SUNY HLTH SCI CTR, DEPT BIOCHEM, BROOKLYN, NY 11203 USA
[2] UNIV CALIF SAN DIEGO, DEPT MED, DIV ENDOCRINOL & METAB, SAN DIEGO, CA 92103 USA
[3] UNIV CALIF SAN FRANCISCO, METAB RES UNIT, SAN FRANCISCO, CA 94143 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1996年 / 271卷 / 05期
关键词
retinoic acid; transcriptional control; nuclear receptors;
D O I
10.1152/ajpcell.1996.271.5.C1750
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Na-K-ATPase alpha(3)-subunit mRNA levels are both positively and negatively controlled by thyroid hormone [3,5,3'triiodothyronine (T-3)] in primary cultures of neonatal rat cardiac myocytes. In this study, transient transfection analysis indicated that two regions of the rat alpha(3) gene between nucleotides -116 and -6 and -6 and +80 conferred T-3-mediated inhibition of reporter gene expression. Electrophoretic mobility shift assays showed specific binding of T-3 receptor monomers and T-3 receptor-retinoid X receptor heterodimers at each alpha(3) gene negative T-3-response region. The alpha(3) gene region from -116 to -6 base pairs also mediates repression in response to retinoic acid (RA) and binds RA receptor. In the absence of ligand, reporter gene expression driven by the -116- to -6-base pair region is repressed with cotransfection of T-3 receptor, whereas it is unaffected by overexpression of RA receptor. These data demonstrate that the proximal promoter of the rat Na-K-ATPase alpha(3) gene contains sequence motifs that mediate repression of alpha(3) gene transcription in response to either T-3 or RA in neonatal rat cardiac myocytes.
引用
收藏
页码:C1750 / C1756
页数:7
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