Triiodothyronine-mediated myosin heavy chain gene transcription in the heart

被引:43
作者
Danzi, S
Ojamaa, K
Klein, I
机构
[1] NYU, N Shore Univ Hosp, Sch Med, Div Endocrinol, Manhasset, NY 11030 USA
[2] NYU, N Shore Univ Hosp, Sch Med, Dept Med, Manhasset, NY 11030 USA
[3] NYU, Sch Med, Dept Cell Biol, New York, NY 10021 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2003年 / 284卷 / 06期
关键词
cardiac contractility; heterogeneous nuclear ribonucleic acid; thyroid hormone; thyroid disease;
D O I
10.1152/ajpheart.00860.2002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We developed an RT-PCR assay to study both the time course and the mechanism for the triiodothyronine (T-3)-induced transcription of the alpha- and beta-myosin heavy chain (MHC) genes in vivo on the basis of the quantity of specific heterogeneous nuclear RNA (hnRNA). The temporal relationship of changes in transcriptional activity to the amount of alpha-MHC mRNA and the coordinated regulation of transcription of more than one gene in response to T-3 are demonstrated here for the first time. Quantitation of alpha-MHC hnRNA demonstrated that T-3 induced alpha-MHC transcription in hypothyroid rats within 30 min of a single injection of T-3 (0.5 mug/100 g body wt). Maximal transcription rates (135% +/- 15.8 of euthyroid values) occurred 6 h after injection and subsequently declined in parallel with serum T-3 levels. The transcription of beta-MHC was reduced to 86% of peak hypothyroid levels 6 h after a single T-3 injection and reached a nadir of 59% of hypothyroid levels at 36 h. Analysis of the time course of T-3-mediated induction of alpha-MHC hnRNA and repression of beta-MHC hnRNA indicates that separate molecular mechanisms are involved in the coordinated regulation of these genes.
引用
收藏
页码:H2255 / H2262
页数:8
相关论文
共 39 条
[1]   EFFECT OF THYROID STATE ON MYOCARDIAL CONTRACTILITY AND VENTRICULAR EJECTION RATE IN MAN [J].
AMIDI, M ;
LEON, DF ;
DEGROOT, WJ ;
KROETZ, FW ;
LEONARD, JJ .
CIRCULATION, 1968, 38 (02) :229-&
[2]   Thyroid hormone regulation of myocardial Na/K-ATPase gene expression [J].
Awais, D ;
Shao, Y ;
Ismail-Beigi, F .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2000, 32 (11) :1969-1980
[3]   TIME COURSE OF THE INVIVO EFFECTS OF THYROID-HORMONE ON CARDIAC GENE-EXPRESSION [J].
BALKMAN, C ;
OJAMAA, K ;
KLEIN, I .
ENDOCRINOLOGY, 1992, 130 (04) :2001-2006
[4]  
BOHELER KR, 1992, J BIOL CHEM, V267, P12979
[5]  
BRENT GA, 1994, NEW ENGL J MED, V331, P847
[6]   A prospective randomized clinical study of thyroid hormone treatment after operations for complex congenital heart disease [J].
Chowdhury, D ;
Ojamaa, K ;
Parnell, VA ;
McMahon, C ;
Sison, CP ;
Klein, I .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2001, 122 (05) :1023-1025
[7]   NONINVASIVE EVALUATION OF CARDIAC-FUNCTION IN HYPOTHYROIDISM - RESPONSE TO GRADUAL THYROXINE REPLACEMENT [J].
CROWLEY, WF ;
RIDGWAY, EC ;
BOUGH, EW ;
FRANCIS, GS ;
DANIELS, GH ;
KOURIDES, IA ;
MYERS, GS ;
MALOOF, F .
NEW ENGLAND JOURNAL OF MEDICINE, 1977, 296 (01) :1-6
[8]   ACUTE CELLULAR ACTIONS OF THYROID-HORMONE AND MYOCARDIAL-FUNCTION [J].
DAVIS, PJ ;
DAVIS, FB .
ANNALS OF THORACIC SURGERY, 1993, 56 (01) :S16-S23
[9]   BIOCHEMICAL BASIS OF THYROID-HORMONE ACTION IN THE HEART [J].
DILLMANN, WH .
AMERICAN JOURNAL OF MEDICINE, 1990, 88 (06) :626-630
[10]  
Elferink CJ, 1996, BIOTECHNIQUES, V20, P470