Complete primary structure and tissue expression of chicken pectoralis M-protein

Jiro Noguchi, Masashi Yanagisawa, Michihiro Imamura, Yoshitoshi Kasuya, Takeshi Sakurai, Takeshi Tanaka, Tomoh Masaki

Research output: Contribution to journalArticlepeer-review

46 Scopus citations

Abstract

M-Protein (165 kDa) is a structural constituent of myofibrillar M-band in striated muscle. We generated a monoclonal antibody which recognized a 165-kDa protein from chicken pectoralis muscle in immunoblot analysis and stained the M-band under immunofluorescence microscopy. By screening a λgt11 cDNA library from chicken embryonic pectoralis muscle with this antibody, we isolated a cDNA clone encoding the M-protein. Northern blot analysis showed that M-protein mRNA is expressed in pectoralis and cardiac muscle but not in gizzard smooth muscle or non-muscle tissues. Moreover, the anterior latissimus dorsi muscle, which consists almost exclusively of slow fiber types, contains no detectable levels of the mRNA. The full-length cDNA sequence predicted a 1,450-ammo acid polypeptide with a calculated molecular weight of 163 × 103. The encoded protein contains several copies of two different repetitive motifs: five copies of fibronectin type III repeats are in the middle part of the predicted molecule, and two and four copies of the immunoglobulin C2-type repeats are located toward the NH2-terminal and COOH-terminal regions, respectively. This indicates that M-protein, along with other thick filament-associated proteins such as C-protein, twichin, and titin, belongs to the superfamily of cytoskeletal proteins with immunoglobulin/fibronectin repeats.

Original languageEnglish (US)
Pages (from-to)20302-20310
Number of pages9
JournalJournal of Biological Chemistry
Volume267
Issue number28
StatePublished - Oct 5 1992

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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