MCL-1V, a novel mouse antiapoptotic MCL-1 variant, generated by RNA splicing at a non-canonical splicing pair

被引:8
|
作者
Kojima, Shogo [2 ]
Hyakutake, Akira [2 ]
Koshikawa, Nobuko [2 ]
Nakagawara, Akira [1 ]
Takenaga, Keizo [2 ,3 ]
机构
[1] Chiba Canc Res Inst, Div Biochem & Innovat Canc Therapeut, Chuoh Ku, Chiba 2608717, Japan
[2] Chiba Canc Res Inst, Lab Canc Metastasis, Chuoh Ku, Chiba 2608717, Japan
[3] Shimane Univ, Fac Med, Dept Life Sci, Izumo, Shimane 6938501, Japan
关键词
Mcl-1; Mcl-1V; Splicing variant; Non-canonical; Apoptosis; LEWIS LUNG-CARCINOMA; TUMOR-CELLS; EXPRESSION; APOPTOSIS; PHOSPHORYLATION; GENE; TANKYRASE-1; PROTEINS; DOMAIN; SITES;
D O I
10.1016/j.bbrc.2009.11.086
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Myeloid cell leukemia-1 (MCL-1) that belongs to BCL-2 family is essential for Survival of hematopoietic stein cells It is upregulated in various types of cancer and promotes cancer cell metastasis. It is known chat human MCL-1 gene undergoes differential splicing and yields three mRNAs encoding antiapoptotic MCL-1L and proapoptotic MCL-1S and MCL-1ES However, no MCL-1 variants have been reported in mousecells We report here anew splicing variant of mouse Mcl-1, Mc1-1V, that is expressed in a variety of mouse normal and tumor cell lines and tissues. Comparative sequence analysis of the full-length Mcl-1 and Mcl-1V cDNAs suggested that Mcl-1V mRNA results from splicing within the first coding exon of Mcl-1 gene at a non-canonical donor-acceptor pair. MCL-1V lacks 46 amino acid residues within the N-terminal region of MCL-1. It localizes in mitochondria and inhibits anoxia- and anticancer drug-induced apoptosis as potent as MCL-1, and decayed less rapidly than MCL-1 in the cells undergoing apoptosis. Collectively, our results show that mouse cells ubiquitously express antiapoptotic MCL-1V that may play a role in mitochondrial cell death. (C) 2009 Elsevier Inc All rights reserved.
引用
收藏
页码:492 / 497
页数:6
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