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PMID: 2249844 Published · ppublish English Comparative Study Journal Article

The complete sequence of the human beta-myosin heavy chain gene and a comparative analysis of its product.

Genomics ·Vol. 8 ·No. 2 ·1990-10-00 ·Pages 194-206

Jaenicke T, Diederich KW, Haas W, Schleich J, Lichter P, Pfordt M, Bach A, Vosberg HP

Abstract

We have isolated and sequenced the gene and the cDNA coding for the human cardiac beta-myosin heavy chain (designated MYH7). The gene is 22,883 bp long. The 1935 amino acids of this protein (Mr223,111) are encoded by 38 exons. The 5' untranslated region (86 bp) is split by two introns. The 3' untranslated region is 114 bp long. Three Alu repeats were identified within the gene and a fourth one in the 3' flanking intergenic region. The molecular organization of this gene reflects the conservative pattern with respect to size, coding ratio, and number or position of introns characteristic of vertebrate sarcomeric myosin heavy chain genes. The protein sequence of the human beta-heavy chain was compared with corresponding (homologous) sequences of rabbit, rat, and hamster as well as with the (heterologous) embryonic heavy chain sequences of rat, chicken, and man. The results show that protein subregions responsible for basic functions of myosin heavy chains (nucleotide binding and actin binding) are very similar in homologous and heterologous heavy chains. Regions that differ in their primary sequences in heterologous heavy chains appear to be highly conserved within mammalian beta-myosin heavy chains. Constant and variable subregions of heavy chains are discussed in terms of functional significance and evolutionary relatedness.

MeSH Terms
Amino Acid Sequence Animals Base Sequence DNA/genetics Genes Humans Mammals/genetics Molecular Sequence Data Myosins/genetics Phylogeny Regulatory Sequences, Nucleic Acid Sequence Homology, Nucleic Acid Species Specificity
Chemicals
DNA Myosins
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Jaenicke T
Max-Planck-Institut for Medical Research, Department of Cell Physiology, Heidelberg, Federal Republic of Germany.
Diederich K W
Haas W
Schleich J
Lichter P
Pfordt M
Bach A
Vosberg H P
Article Info
Journal
Genomics
Abbr.
Genomics
ISSN
0888-7543
Published
1990-10-00
Pages
194-206
Language
English
Region
United States
NLM ID
8800135
Subset
IM
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M57965, M58018
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