Gueth-Hallonet C, Weber K, Osborn M
Department of Biochemistry, Max Planck Institute for Biophysical Chemistry, Goettingen, Germany.
Exp Cell Res. 1997 May 25;233(1):21-4. doi: 10.1006/excr.1997.3557.
NuMA is a component of the nuclear matrix which may play a structural role in the architecture of the interphase nucleus. During apoptosis NuMA is redistributed within the nucleus and is proteolysed from a 238-kDa form to a 180- to 200-kDa form. Here we show that the cleavage site leading to the stable fragment occurs between residues 1701 and 1725. Both the changes in morphology associated with apoptosis and the cleavage of NuMA were retarded by treatment with TPCK but not by treatment by other protease inhibitors including ICE inhibitor II.
核有丝分裂器蛋白(NuMA)是核基质的一个组成部分,可能在间期细胞核的结构中起结构性作用。在细胞凋亡过程中,NuMA在细胞核内重新分布,并从238 kDa的形式被蛋白水解为180至200 kDa的形式。在此我们表明,导致稳定片段产生的切割位点位于1701和1725位残基之间。与细胞凋亡相关的形态变化以及NuMA的切割都因用对甲苯磺酰苯丙氨酰氯甲酮(TPCK)处理而延迟,但用包括ICE抑制剂II在内的其他蛋白酶抑制剂处理则无此效果。