Caspases mediate nucleoporin cleavage, but not early redistribution of nuclear transport factors and modulation of nuclear permeability in apoptosis

被引:89
作者
Ferrando-May, E
Cordes, V
Biller-Ckovric, I
Mirkovic, J
Görlich, D
Nicotera, P
机构
[1] Univ Konstanz, Dept Biol, Chair Mol Toxicol, D-78457 Constance, Germany
[2] Karolinska Inst, Med Nobel Inst, Dept Cellular & Mol Biol, S-17177 Stockholm, Sweden
[3] German Canc Res Ctr, Div Cell Biol, D-69120 Heidelberg, Germany
[4] Univ Heidelberg, Zentrum Mol Biol, D-69120 Heidelberg, Germany
[5] Univ Leicester, MRC, Toxicol Unit, Leicester LE1 9HN, Leics, England
关键词
caspase; nuclear pore complex; nuclear import; mRNA export; microinjection;
D O I
10.1038/sj.cdd.4400837
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
In eukaryotic cells, both soluble transport factors and components of the nuclear pore complex mediate protein and RNA trafficking between the nucleus and the cytoplasm, Here, we investigated whether caspases, the major execution system in apoptosis, target the nuclear pore or components of the nuclear transport machinery. Four nucleoporins, Nup153, RanBP2, Nup214 and Tpr are cleaved by caspases during apoptosis, In contrast, the nuclear transport factors, Ran, importin alpha and importin beta are not proteolytically processed, but redistribute across the nuclear envelope independently and prior to caspase activation. Also, mRNA accumulates into the nucleus before caspases become active. Microinjection experiments further revealed that early in apoptosis, the nucleus becomes permeable to dextran molecules of 70 kD molecular weight. Redistribution; of import factors and mRNA, as well as nuclear permeabilisation, occur prior to caspase-mediated nucleoporin cleavage, Our findings suggest that the apoptotic programme includes modifications in the machinery responsible for nucleocytoplasmic transport, which are independent from caspase-mediated degradation of nuclear proteins.
引用
收藏
页码:495 / 505
页数:11
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