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Enhanced apoptosis by a novel gene, Bak-like, that lacks the BH3 domain.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2004 Mar 26; Vol. 316 (1), pp. 18-23. - Publication Year :
- 2004
-
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.
- Subjects :
- Alternative Splicing
Amino Acid Sequence
Animals
Base Sequence
Gene Library
HeLa Cells
Humans
Membrane Proteins chemistry
Membrane Proteins metabolism
Mice
Mitochondria metabolism
Molecular Sequence Data
Neoplasms genetics
Neoplasms metabolism
Protein Structure, Tertiary
Protein Transport
Proto-Oncogene Proteins
RNA, Messenger metabolism
Sequence Alignment
bcl-2 Homologous Antagonist-Killer Protein
Apoptosis
Membrane Proteins genetics
Membrane Proteins physiology
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 316
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 15003505
- Full Text :
- https://doi.org/10.1016/j.bbrc.2004.01.173