PKC zeta controls DNA topoisomerase-dependent human caspase-2 pre-mRNA splicing

被引:10
|
作者
Solier, Stephanie [2 ,3 ]
De Cian, Marie Cecile [1 ]
Bettaleb, Ali [2 ,4 ]
Desoche, Lydie [2 ]
Solary, Eric [2 ]
Corcos, Laurent [1 ,2 ]
机构
[1] Fac Med, Inserm U613 EA948, F-29238 Brest 3, France
[2] Fac Med, Inserm U517, Dijon, France
[3] CHRU Le Bocage, Serv Hematol Clin, Dijon, France
[4] Ecole Prat Hautes Etud, Paris, France
关键词
caspase-2; mRNA splicing; PKC zeta; topoisomerase; cell cycle;
D O I
10.1016/j.febslet.2007.12.032
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
Caspase-2 exists as two main isoforms: the caspase-2L long isoform, which is pro-apoptotic, and the caspase-2S short isoform, which may be anti-apoptotic. Topoisomerase inhibitors drive inclusion of exon 9, specific for Casp-2S mRNA, and lower Casp-2S mRNA and protein. With cell lines engineered to express various PKC isoforms, we demonstrate that PKC zeta, but not PKCalpha, positively regulates Casp-2S mRNA assembly triggered by topoisomerase inhibitors. In addition, exon 9 inclusion is lowered in mitosis but increased in the G1/S phase. Hence, the control of caspase-2 exon 9 inclusion by topoisomerase inhibitors depends on phosphorylation and/or dephosphorylation events, and on the cell cycle phase. (C) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:372 / 378
页数:7
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