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IEX-1-induced cell death requires BIM and is modulated by MCL-1
Authors:Seongmin Yoon  Yong-Hak Kim  Mira Park  Kangseok Lee  Jeehyeon Bae
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
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.
Keywords:Apoptosis   BCL-2 family   MCL-1   IEX-1   BIM
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