| Literature DB >> 15003505 |
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.Entities:
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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