Title of article :
Thyroid Hormone Regulates Slow Skeletal Troponin I Gene Inactivation in Cardiac Troponin I Null Mouse Hearts
Author/Authors :
Xupei Huang، نويسنده , , Kevin J. Lee، نويسنده , , Beth Riedel، نويسنده , , Chi Zhang، نويسنده , , Larry F. Lemanski، نويسنده , , Jeffery W. Walker، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2000
Pages :
8
From page :
2221
To page :
2228
Abstract :
Two main troponin I genes, cardiac (cTnI) and slow skeletal (ssTnI), are expressed in the mammalian heart under the control of a developmentally regulated program. ssTnI is expressed first in embryonic and fetal heart, and is then downregulated by an unknown mechanism after birth. Unlike other contractile protein genes, ssTnI is not re-expressed during hypertrophy or end-stage heart failure in rats and humans. In the present study, we also show that ssTnI re-expression does not occur in hypertrophic mouse heart. To investigate ssTnI downregulation further, cTnI knockout mice were used to examine a possible role for thyroid hormone. Northern blot analysis of euthyroid animals showed a time-dependent loss of ssTnI mRNA that was similar for wild-type, heterozygous and homozygous cTnI mutant mice. In cTnI null mice made hyperthyroid by -thyroxine, the duration of ssTnI expression assessed by both mRNA and protein content was abbreviated compared with the euthyroid group. Hyperthyroid cTnI null mice also died significantly earlier than euthyroids (postnatal day 14 v day 18). In cTnI null mice made hypothyroid by addition of phenylthiouracil to the drinking water, ssTnI expression was prolonged and mice survived until day 20 or 21. Overall, the results indicate that inactivation of the ssTnI gene occurs even in the absence of cTnI mRNA and protein indicating that these are not critical signals for ssTnI down regulation in the heart. In contrast, thyroid hormone influences the time course of ssTnI expression and the life span of cTnI null mice probably through a transcriptional regulation of ssTnI in the heart.
Keywords :
Isoform switching , Heart development. , Gene regulation , Troponin I , Thyroid hormone
Journal title :
Journal of Molecular and Cellular Cardiology
Serial Year :
2000
Journal title :
Journal of Molecular and Cellular Cardiology
Record number :
527361
Link To Document :
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