Differential subcellular localization of functionally divergent survivin splice variants

被引:135
作者
Mahotka, C
Liebmann, J
Wenzel, M
Suschek, CV
Schmitt, M
Gabbert, HE
Gerharz, CD
机构
[1] Univ Dusseldorf, Inst Pathol, D-40225 Dusseldorf, Germany
[2] Univ Dusseldorf, Inst Immunobiol, D-40225 Dusseldorf, Germany
[3] Univ Dusseldorf, Dept Gastroenterol Hepatol & Infectiol, D-40225 Dusseldorf, Germany
关键词
survivin; apoptosis; alternative splicing; cancer;
D O I
10.1038/sj.cdd.4401091
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
Survivin is an inhibitor of apoptosis protein (IAP) that is markedly overexpressed in most cancers. We identified two novel functionally divergent splice variants, i.e. non-anti-apoptotic survivin-2B and antiapoptotic survivin-DeltaEx3. Because survivin-2B might be a naturally occurring antagonist of antiapoptotic survivin variants, we analyzed the subcellular distribution of these proteins. PSORT 11 analysis predicted a preferential cytoplasmic localization of survivin and survivin-2B, but a preferential nuclear localization of survivin-DeltaEx3. GFP-tagged survivin variants confirmed the predicted subcellular localization and additionally revealed a cell cycle-dependent nuclear accumulation of survivin-DeltaEx3 . Moreover, a bipartite nuclear localization signal found exclusively in survivin-DeltaEx3 may support cytoplasmic clearance of survivin-DeltaEx3. In contrast to the known association between survivin and microtubules or Centromeres during mitosis, no corresponding co-localization became evident for survivin-DeltaEx3 or survivin-2B. In conclusion, our study provided data on a differential subcellular localization of functionally divergent survivin variants, suggesting that survivin isoforms may perform different functions in distinct subcellular compartments and distinct phases of the cell cycle.
引用
收藏
页码:1334 / 1342
页数:9
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