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Identification and characterization of Bimγ, a novel proapoptotic BH3-only splice variant of Bim

  • Jun Wei Liu
  • , Dhyan Chandra
  • , Shao Hua Tang
  • , Dharam Chopra
  • , Dean G. Tang

Research output: Contribution to journal › Article › peer-review

Abstract

BH3 (Bcl-2 homology 3)-only proteins of the Bcl-2 family play an essential role in apoptosis. In this study, a novel human BH3-only protein, Bcl-2-interacting mediator (Bim)γ, was identified during our study of regulation of prostate cancer cell death by Bcl-2 family proteins. Bimγ shares the highest amino acid sequence homology to BimEL and BimL, two proapoptotic BH3-only Bcl-2 proteins derived from alternative mRNA splicing. Genomic studies indicate that Bimγ is a novel splice variant of Bim and is generated as a result of the retention of a 126-bp intron of the bim gene. Bimγ mRNA displays a tissue-specific expression pattern distinct from those of the other Bim isoforms. Subcellular fractionation studies indicate that Bimγ is localized both in intracellular membranes and cytosol. Interestingly, Bimγ mRNA, similar to the BimEL protein, is up-regulated in the majority of the prostate cancer cell lines studied, whereas several other proapoptotic Bcl-2 proteins, including Bax, Bak, and Bad, are down-regulated in prostate cancer cells. Functional studies indicate that Bimγ inhibits clonal growth in prostate cancer cells and promotes apoptosis, which is inhibited by overexpressing Bcl-2. Because both Bimγ and BimEL are proapoptotic BH3-only proteins and both are up-regulated in prostate cancer cells, they may play a unique role in prostate cancer development.

Original languageEnglish (US)
Pages (from-to)2976-2981
Number of pages6
JournalCancer Research
Volume62
Issue number10
StatePublished - May 15 2002

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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