A novel beta 1 integrin isoform produced by alternative splicing: unique expression in cardiac and skeletal muscle

FEBS Lett. 1995 Aug 7;369(2-3):340-4. doi: 10.1016/0014-5793(95)00814-p.

Abstract

The mRNA's of several integrin subunits are alternatively spliced in the region encoding cytoplasmic domains, that may potentially provide alternative integrin-cytoskeleton interactions and transmembrane signaling pathways. We identified a novel cytoplasmic tail variant of the human beta 1 subunit by reverse transcriptase polymerase chain reaction. This fourth beta 1 variant, named beta 1D, is specific for skeletal and cardiac muscle. The determined genomic organization of the 3'-region of the human beta 1 gene reveals that beta 1D is produced by alternative splicing of mRNA. In addition, we show that the expression of beta 1D is developmentally regulated during murine myoblast differentiation, suggesting a role for beta 1D in myogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing*
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cell Differentiation
  • Cells, Cultured
  • Cloning, Molecular
  • Cytoplasm / chemistry
  • Gene Expression Regulation, Developmental*
  • Genes / genetics
  • Humans
  • Integrin beta1
  • Integrins / chemistry
  • Integrins / genetics*
  • Mice
  • Molecular Sequence Data
  • Muscle, Skeletal / chemistry*
  • Myocardium / chemistry*
  • Organ Specificity
  • Polymerase Chain Reaction / methods
  • RNA, Messenger / analysis
  • Sequence Analysis, DNA

Substances

  • Integrin beta1
  • Integrins
  • RNA, Messenger

Associated data

  • GENBANK/U28252