A novel SREBP-1 splice variant: tissue abundance and transactivation potency

Biochim Biophys Acta. 2005 Oct 15;1731(1):41-7. doi: 10.1016/j.bbaexp.2005.08.004. Epub 2005 Aug 29.

Abstract

Sterol regulatory element binding proteins (SREBPs) belong to the family of basic helix-loop-helix-leucine zipper transcription factors. The SREBP-1 gene encodes two different isoforms, SREBP-1a and -1c, that are expressed at varying levels in different tissues and cultured cells and exhibit common and distinct functions. We identified an additional SREBP-1 isoform, termed SREBP-1ac, and determined its mRNA abundance in different human tissues and cell lines. SREBP-1ac mRNA was detectable in all tissues studied, although at lower levels than the major SREBP-1a and -1c isoforms. Transcription of the novel SREBP isoform was not induced by insulin or cholesterol depletion. SREBP-1ac did not transactivate the human LDLR and UCP2 promoters but robustly attenuated the transactivation capacity of SREBP-1a, -1c and -2 in cotransfection experiments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / metabolism
  • Alternative Splicing
  • Amino Acid Sequence
  • Brain / metabolism
  • Cell Line
  • Humans
  • Liver / metabolism
  • Male
  • Molecular Sequence Data
  • Protein Isoforms / chemistry
  • Protein Isoforms / metabolism
  • Sterol Regulatory Element Binding Protein 1 / chemistry
  • Sterol Regulatory Element Binding Protein 1 / genetics*
  • Sterol Regulatory Element Binding Protein 1 / metabolism*
  • Testis / metabolism
  • Tissue Distribution
  • Transcriptional Activation*
  • Transfection

Substances

  • Protein Isoforms
  • SREBF1 protein, human
  • Sterol Regulatory Element Binding Protein 1