Both a ubiquitous factor mTEF-1 and a distinct muscle-specific factor bind to the M-CAT motif of the myosin heavy chain β gene
Open Access
- 1 January 1993
- journal article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 21 (17) , 4103-4110
- https://doi.org/10.1093/nar/21.17.4103
Abstract
The A element, a fourteen base pair sequence in the rabbit myosin heavy chain (HC) β promoter (-276/- 263), contains the M-CAT motif, a cis-acting element found in several muscle-specific genes. The A element is essential for muscle-specific transcription of the myosin HCβ gene. Recently, we have identified both muscle-specific and ubiquitous factors (A1 and A2 factors, respectively) that bind to the A element. Since the sequence of the A element is very similar to the GTIIC motif In the SV40 enhancer, we examined the relationship between A-element-binding factors and a GTIIC binding factor TEF-1, recently isolated from HeLa cells. The GTIIC motif was bound by the A1 and A2 factors in muscle nuclear extracts and competed with the A element for DNA-protein complex formation. Antibody against human TEF-1 'supershifted' the ubiquitous A2 factor- DNA complex, but did not alter the mobility of the muscle-specific A1 factor-DNA complex. We Isolated a murine cDNA clone (mTEF-1) from a cardiac cDNA library. The clone is highly homologous to Hela cell TEF-1. The In vitro transcription/translation product of mTEF-1 cDNA bound to the A element, and the DNA binding property of mTEF-1 was Identical to that of the A2 factor. Transfection of mTEF-1 cDNA into muscle and non-muscle cells confirmed that mTEF-1 corresponds to A2, but not to A1 factors. The mTEF-1 mRNA Is expressed abundantly in skeletal and cardiac muscles, kidney and lung, but it is also expressed at lower levels in other tissues. These results suggest that the M-CAT binding factors consist of two different factors; the ubiquitous A2 Is encoded by mTEF-1, but the muscle-specific A1 factor is distinct from mTEF-1.Keywords
This publication has 39 references indexed in Scilit:
- Serum response factor p67SRF is expressed and required during myogenic differentiation of both mouse C2 and rat L6 muscle cell lines.The Journal of cell biology, 1992
- Cloning, expression, and transcriptional properties of the human enhancer factor TEF-1Cell, 1991
- The myoD Gene Family: Nodal Point During Specification of the Muscle Cell LineageScience, 1991
- A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutationPublished by Elsevier ,1990
- A molecular basis for familial hypertrophic cardiomyopathy: An αβ cardiac myosin heavy chain hybrid geneCell, 1990
- Myogenin, a factor regulating myogenesis, has a domain homologous to MyoDCell, 1989
- Expression of a single transfected cDNA converts fibroblasts to myoblastsPublished by Elsevier ,1987
- Isolation of biologically active ribonucleic acid from sources enriched in ribonucleaseBiochemistry, 1979
- Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.Proceedings of the National Academy of Sciences, 1979
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970