Complete sequence of human fast‐type and slow‐type muscle myosin‐binding‐protein C (MyBP‐C)
- 1 September 1993
- journal article
- Published by Wiley in European Journal of Biochemistry
- Vol. 216 (2), 661-669
- https://doi.org/10.1111/j.1432-1033.1993.tb18186.x
Abstract
Myosin-binding-protein C (MyBP-C) is a myosin-associated protein of unknown function found in the cross-bridge-bearing zone (C region) of A bands in striated muscle. Using a cDNA clone encoding the fast-type isoform of chicken MyBP-C, we screened a human fetal muscle cDNA library and isolated clones encoding the full-length human fast-type isoform of MyBP-C. cDNA clones encoding the slow-type isoform of human MyBP-C, were also isolated and fully sequenced. Northern-blot analysis demonstrated skeletal muscle-specific expression of these gene products. Using human/hamster somatic-cell hybrids, we were able to map the slow-type MyBP-C to human chromosome 12, and the fast-type MyBP-C to chromosome 19. The cDNA for human fast-type MyBP-C encodes a polypeptide of 1142 amino acids with an expected molecular mass of 128.1 kDa. Comparison of this cDNA with other members of the MyBP family reveals extensive primary-sequence conservation. Each MyBP-C contains seven immunoglobulin C2 motifs and three fibronectin type-III repeats in the arrangement C2-C2-C2-C2-C2-III-III-C2-III-C2. Regions of high identity shared by the chicken and the two human proteins are not restricted to the immunoglobulin and fibronectin motifs. Sequence comparison of all three proteins has allowed us to map a highly conserved region between the first and second C2 motifs, the only large spacer sequence present between motifs in these proteins.Keywords
This publication has 48 references indexed in Scilit:
- Human Myosin-Binding Protein H (MyBP-H): Complete Primary Sequence, Genomic Organization, and Chromospinal LocalizationGenomics, 1993
- Size and charge heterogeneity of C-protein isoforms in avian skeletal muscle. Expression of six different isoforms in chicken muscleJournal of Muscle Research and Cell Motility, 1989
- The Immunoglobulin Superfamily—Domains for Cell Surface RecognitionAnnual Review of Immunology, 1988
- The Immunoglobulin Superfamily: Domains For Cell Surface RecognitionAnnual Review of Immunology, 1988
- Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individualsCell, 1987
- The ultrastructural location of C-protein, X-protein and H-protein in rabbit muscleJournal of Muscle Research and Cell Motility, 1986
- H-protein and X-proteinJournal of Molecular Biology, 1983
- Phosphorylation of a myofibrillar protein of Mr 150 000 in perfused rat heart, and the tentative identification of this as C‐proteinFEBS Letters, 1980
- The binding of skeletal muscle C-protein to F-actin, and its relation to the interaction of actin with myosin subfragment-1Journal of Molecular Biology, 1978
- A new protein of the thick filaments of vertebrate skeletal myofibrilsJournal of Molecular Biology, 1973