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IEX-1-induced cell death requires BIM and is modulated by MCL-1

Authors
Yoon, SeongminHa, Hye-JungKim, Yong-HakWon, MiaePark, MiraKo, Jeong-JaeLee, KangseokBae, Jeehyeon
Issue Date
May-2009
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Apoptosis; BCL-2 family; MCL-1; IEX-1; BIM
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.382, no.2, pp 400 - 404
Pages
5
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
382
Number
2
Start Page
400
End Page
404
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/23191
DOI
10.1016/j.bbrc.2009.03.037
ISSN
0006-291X
1090-2104
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. (C) 2009 Elsevier Inc. All rights reserved.
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자연과학대학 (생명과학과)
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