IEX-1-induced cell death requires BIM and is modulated by MCL-1 |
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Authors: | Seongmin Yoon Yong-Hak Kim Mira Park Kangseok Lee Jeehyeon Bae |
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Affiliation: | a Department of Biomedical Science, College of Life Science, CHA University, 222 Yatap-Dong, Seongnam 463-836, South Korea b Department of Life Science, College of Natural Science, Chung-Ang University, 221 Hueksok-Dong, Seoul 156-756, South Korea c Functional Proteomics Center, KISTS, Seoul 136-791, South Korea |
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Abstract: | MCL-1 (myeloid cell leukemia-1) is a distinguished and pivotal member of the pro-survival BCL-2 family of proteins, and we isolated IEX-1 (immediate early response gene X-1) as a MCL-1-interacting protein using the yeast two-hybrid system and confirmed their endogenous association in human cells. The underlying mechanisms by which IEX-1 affects cell survival and death are largely unknown. Ectopic expression of IEX-1-induced caspase-dependent apoptosis in 293T cells, and the response was significantly modulated by changes in the MCL-1 expression level in cells. Forced expression of IEX-1 was unable to induce cell death or to perturb mitochondrial membrane potential in BIM-depleted cells. Additionally, knockouts of NOXA or PUMA did not affect the activities of IEX-1, indicating that the pro-death action of IEX-1 specifically requires BIM. Our findings provide insight into a new regulatory circuit that controls cell death and survival by the coordinated action of MCL-1, IEX-1, and BIM. |
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Keywords: | Apoptosis BCL-2 family MCL-1 IEX-1 BIM |
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