Duan H, Orth K, Chinnaiyan A M, Poirier G G, Froelich C J, He W W, Dixit V M
Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.
J Biol Chem. 1996 Jul 12;271(28):16720-4. doi: 10.1074/jbc.271.28.16720.
Members of the ICE/Ced-3 gene family are likely effector components of the cell death machinery. Here, we characterize a novel member of this family designated ICE-LAP6. By phylogenetic analysis, ICE-LAP6 is classified into the Ced-3 subfamily which includes Ced-3, Yama/CPP32/apopain, Mch2, and ICE-LAP3/Mch3/CMH-1. Interestingly, ICE-LAP6 contains an active site QACGG pentapeptide, rather than the QACRG pentapeptide shared by other family members. Overexpression of ICE-LAP6 induces apoptosis in MCF7 breast carcinoma cells. More importantly, ICE-LAP6 is proteolytically processed into an active cysteine protease by granzyme B, an important component of cytotoxic T cell-mediated apoptosis. Once activated, ICE-LAP6 is able to cleave the death substrate poly(ADP-ribose) polymerase into signature apoptotic fragments.
ICE/Ced-3基因家族的成员可能是细胞死亡机制的效应器组件。在此,我们鉴定了该家族一个名为ICE-LAP6的新成员。通过系统发育分析,ICE-LAP6被归类到Ced-3亚家族,该亚家族包括Ced-3、Yama/CPP32/凋亡蛋白酶、Mch2以及ICE-LAP3/Mch3/CMH-1。有趣的是,ICE-LAP6含有一个活性位点QACGG五肽,而非其他家族成员共有的QACRG五肽。ICE-LAP6的过表达诱导MCF7乳腺癌细胞凋亡。更重要的是,ICE-LAP6被细胞毒性T细胞介导的凋亡的重要组分颗粒酶B蛋白水解加工成一种活性半胱氨酸蛋白酶。一旦被激活,ICE-LAP6就能将死亡底物聚(ADP-核糖)聚合酶切割成典型的凋亡片段。