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Actin, alpha skeletal muscle

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Actin, alpha skeletal muscle
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Actin, alpha skeletal muscle is a protein that in humans is encoded by the ACTA1 gene.[5][6]

Quick Facts ACTA1, Available structures ...
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Actin alpha 1 which is expressed in skeletal muscle is one of six different actin isoforms which have been identified. Actins are highly conserved proteins that are involved in cell motility, structure and integrity. Alpha actins are a major constituent of the contractile apparatus.[7]

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Skeletal actin gene expression

Skeletal alpha actin expression is induced by stimuli and conditions known to cause muscle formation.[8] Such conditions result in fusion of committed cells (satellite cells) into myotubes, to form muscle fibers. Skeletal actin itself, when expressed, causes expression of several other "myogenic genes", which are essential to muscle formation.[9] One key transcription factor that activates skeletal actin gene expression is Serum Response Factor ("SRF"), a protein that binds to specific sites on the promoter DNA of the actin gene.[10] SRF may bring a number of other proteins to the promoter of skeletal actin, such as androgen receptor, and thereby contribute to induction of skeletal actin gene expression by androgenic (often termed "anabolic") steroids.[11]

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Interactions

Actin, alpha 1 has been shown to interact with TMSB4X,[12][13] MIB2[14] and PRKCE.[15]

Clinical significance

Mutations in the ACTA1 gene are known to cause the following conditions:[16]

  • Nemaline myopathy 3 (NEM3);
  • Myopathy, actin, congenital, with excess of thin myofilaments (MPCETM);
  • Myopathy, congenital, with fiber-type disproportion (CFTD);
  • Myopathy, scapulohumeroperoneal (SHPM).

See also

References

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Further reading

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