1. Human homologue of S. pombe Rad9 interacts with BCL-2/BCL-xL and promotes apoptosis.
- Author
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Komatsu K, Miyashita T, Hang H, Hopkins KM, Zheng W, Cuddeback S, Yamada M, Lieberman HB, and Wang HG
- Subjects
- Animals, Cell Cycle Proteins analysis, Cell Cycle Proteins genetics, Cell Cycle Proteins metabolism, Cell Nucleus chemistry, Cell Survival genetics, Flow Cytometry, Humans, Indicators and Reagents, Mammals, Molecular Sequence Data, Plasmids, Propidium, Proto-Oncogene Proteins c-bcl-2 analysis, Proto-Oncogene Proteins c-bcl-2 genetics, RNA, Antisense pharmacology, Schizosaccharomyces metabolism, Sequence Homology, Amino Acid, Signal Transduction physiology, Transfection, Two-Hybrid System Techniques, bcl-X Protein, Apoptosis genetics, Proto-Oncogene Proteins c-bcl-2 metabolism, Schizosaccharomyces cytology, Schizosaccharomyces genetics
- Abstract
DNA damage induces apoptosis through a signalling pathway that can be suppressed by the BCL-2 protein, but the mechanism by which DNA damage does this is unknown. Here, using yeast two-hybrid and co-immunoprecipitation studies, we show that RAD9, a human protein involved in the control of a cell-cycle checkpoint, interacts with the anti-apoptotic Bcl-2-family proteins BCL-2 and BCL-x L, but not with the pro-apoptotic BAX and BAD. When overexpressed in mammalian cells, RAD9 induces apoptosis that can be blocked by BCL-2 or BCL-x L. Conversely, antisense RAD9 RNA suppresses cell death induced by methyl methanesulphonate. These findings indicate that RAD9 may have a new role in regulating apoptosis after DNA damage, in addition to its previously described checkpoint-control and other radioresistance-promoting functions.
- Published
- 2000
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