Vascular smooth muscle expresses a truncated Na+,K+-ATPase α-1 subunit isoform

Russell M. Medford, Ronald Hyman, Mushtaq Ahmad, Julius C. Allen, Thomas A. Pressley, Paul D. Allen, Bernardo Nadal-Ginard

Research output: Contribution to journalArticle

44 Scopus citations

Abstract

By regulating transmembrane Na+ and K+ concentrations and membrane potential, the Na+,K+-ATPase plays an important role in regulating cardiac, skeletal, and smooth muscle function. A high degree of amino acid sequence and structural identity characterizes the three Mr 100,000 Na+,K+-ATPase α subunit isoforms expressed in cardiac and skeletal muscle. Strikingly, vascular smooth muscle utilizes alternative RNA processing of the α-1 gene to express a structurally distinct Mr ∼65,000 isoform, α-1-T (truncated). Analysis of both its mRNA and protein structure reveals that α-1-T encodes only the first 554 amino acids of α-1 to Gly554, then terminates with an intron-encoded 27-residue peptide. By Western blot analysis, α-1-T represents a major, evolutionarily conserved, truncated Na+,K+-ATPase isoform expressed in vascular smooth muscle. This demonstrates an unexpected complexity in the regulation of vascular smooth muscle Na+,K+-ATPase gene expression and suggests that a structurally novel, truncated a subunit may play a role in vascular smooth muscle active ion transport.

Original languageEnglish (US)
Pages (from-to)18308-18312
Number of pages5
JournalJournal of Biological Chemistry
Volume266
Issue number27
StatePublished - Sep 25 1991
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry

Fingerprint Dive into the research topics of 'Vascular smooth muscle expresses a truncated Na<sup>+</sup>,K<sup>+</sup>-ATPase α-1 subunit isoform'. Together they form a unique fingerprint.

  • Cite this

    Medford, R. M., Hyman, R., Ahmad, M., Allen, J. C., Pressley, T. A., Allen, P. D., & Nadal-Ginard, B. (1991). Vascular smooth muscle expresses a truncated Na+,K+-ATPase α-1 subunit isoform. Journal of Biological Chemistry, 266(27), 18308-18312.