An anti-sense c-erbA clone inhibits thyroid hormone-induced expression from the alpha-myosin heavy chain promoter

J Biol Chem. 1990 Apr 15;265(11):6489-93.

Abstract

The effects of thyroid hormone on expression of cardiac myosin heavy chain genes generally are thought to be mediated by nuclear 3,5,3'-triiodo-L-thyronine (T3) receptors that have been identified as the products of the protooncogene, c-erbA. This hypothesis has been tested by transfection of cardiomyocytes in primary culture with a plasmid, pRSVhEACAT-, expressing anti-sense c-erbA mRNA. Because only a low percentage of cells (20%) could be transfected in primary culture an alpha-myosin heavy chain-chloramphenicol acetyltransferase fusion construct was used as a reporter gene. The results indicate that the anti-sense plasmid almost completely blocks T3-induced activity of the reporter gene (less than 1% control) while transfection of a similar amount of the sense construct, pRSVhEACAT+, has no effect. When the c-erbA plasmids were cotransfected with constructs containing T3-independent promoters, no effects on expression were observed. The combined use of an anti-sense construct and a report gene provides a means of studying the role of c-erbA products in intracellular signal transduction even in differentiated, nondividing cells like those of the heart.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cells, Cultured
  • Cloning, Molecular
  • Female
  • Gene Expression Regulation*
  • Genes / drug effects*
  • Humans
  • Major Histocompatibility Complex
  • Myocardium / metabolism
  • Myosin Subfragments / genetics*
  • Placenta / metabolism
  • Plasmids
  • Pregnancy
  • Promoter Regions, Genetic*
  • Protein-Tyrosine Kinases / genetics
  • Proto-Oncogene Proteins / genetics*
  • Proto-Oncogenes*
  • RNA / genetics*
  • RNA, Antisense
  • RNA, Messenger / antagonists & inhibitors
  • Rats
  • Receptors, Thyroid Hormone / genetics*
  • Transfection
  • Triiodothyronine / pharmacology*

Substances

  • Myosin Subfragments
  • Proto-Oncogene Proteins
  • RNA, Antisense
  • RNA, Messenger
  • Receptors, Thyroid Hormone
  • Triiodothyronine
  • RNA
  • Protein-Tyrosine Kinases