Literature DB >> 15003505

Enhanced apoptosis by a novel gene, Bak-like, that lacks the BH3 domain.

Jin Kyeoung Kim1, Kye Seong Kim, Jung Yong Ahn, Nam Keun Kim, Hyung Min Chung, Hwan Jung Yun, Kwang Yul Cha.   

Abstract

In a variety of physiological settings, cells are eliminated by apoptosis-a genetically encoded process of cellular suicide. Bak, a member of the Bcl-2 protein family, accelerates apoptosis by an unknown mechanism. We have found a novel cDNA encoding a 101-amino acid protein that possesses a Bak-like sequence in our full-length cDNA bank and termed it Bak-like. This protein shares the conserved domains BH1 and BH2 with other pro-apoptotic proteins, but lacks the BH3 domain. Database searches identified this gene on chromosome 6, which could account for the cloned bak and bak-like transcripts by alternative splicing. Bak-like is expressed in a wide variety of tissues. Bak-like is different from bak by Southern blots using probes with or without homology to bak. Despite the loss of the BH3 sequence, bak-like did enhance apoptosis, but was less potent than bak. Confocal microscopy of HeLa cells revealed that EGFP-Bak-like was located diffusely throughout the cytosol. However, upon induction of apoptosis, EGFP-Bak-like redistributed into a punctuate pattern, colocalizing with mitochondria. Like bak, the bak-like gene product directly enhanced apoptotic cell death following an appropriate stimulus.

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Year:  2004        PMID: 15003505     DOI: 10.1016/j.bbrc.2004.01.173

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  1 in total

1.  Bcl-X(L) specifically activates Bak to induce swelling and restructuring of the endoplasmic reticulum.

Authors:  Martina Klee; Felipe X Pimentel-Muiños
Journal:  J Cell Biol       Date:  2005-02-22       Impact factor: 10.539

  1 in total

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