Small mitochondrial ARF (smARF) is located in both the nucleus and cytoplasm, induces cell death, and activates p53 in mouse fibroblasts

被引:10
作者
Ueda, Yuko [1 ]
Koya, Terutsugu [1 ]
Yoneda-Kato, Noriko [1 ]
Kato, Jun-Ya [1 ]
机构
[1] Nara Inst Sci & Technol, Grad Sch Biol Sci, Nara 6300101, Japan
来源
FEBS LETTERS | 2008年 / 582卷 / 10期
关键词
smARF; p53; nuclear localization; MDM2;
D O I
10.1016/j.febslet.2008.03.032
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
The ARF transcript produces two proteins, the full-length ARF, p19(ARF), and a short mitochondrial version, smARF. To explore the functional difference between the two, we generated GFP-fused expression vectors for each protein and introduced them into NIH3T3 murine. broblasts, which sustains a global deletion in the INK4a locus but contains a functional p53 gene. GFP-p19(ARF) was located within the nucleolus as previously reported, whereas GFP-smARF was detected mainly in the nucleoplasm. GFP-smARF induced cell death although to a slightly lesser extent than p19 ARF. GFP-smARF stabilized p53 thereby inducing expression of the target genes, MDM2 and p21. We suggest that smARF has functions other than mitochondria-mediated autophagy, and induces p53 expression and cell death via a novel mechanism. (C) 2008 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1459 / 1464
页数:6
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