Ekert Paul G, Vaux David L
The Walter and Eliza Hall Institute, 1G Royal Parade Parkville, Victoria 3050, Australia.
Curr Opin Cell Biol. 2005 Dec;17(6):626-30. doi: 10.1016/j.ceb.2005.09.001. Epub 2005 Oct 10.
Since the discovery that formation of the apoptosome in mammalian cells is triggered by cytochrome c released from the mitochondria, many other mitochondrial proteins have been suspected to be part of a conspiracy to cause cell death. AIF, EndoG, ANT, cyclophilin D, Bit1, p53AIP, GRIM-19, DAP3, Nur77/TR3/NGFB-1, HtrA2/Omi and Smac/Diablo have all been convicted as killers, but new genetic technology is raising questions about their guilt. Gene knockout experiments suggest that many were wrongly convicted on circumstantial evidence, and just happened to be in the wrong place at the wrong time.
自从发现哺乳动物细胞中凋亡小体的形成是由线粒体释放的细胞色素c触发以来,许多其他线粒体蛋白被怀疑参与了导致细胞死亡的阴谋。凋亡诱导因子(AIF)、核酸内切酶G(EndoG)、腺嘌呤核苷酸转运体(ANT)、亲环蛋白D、Bit1、p53凋亡诱导蛋白(p53AIP)、GRIM-19、死亡相关蛋白3(DAP3)、 Nur77/TR3/NGFβ-1、HtrA2/Omi和Smac/Diablo都被判定为杀手,但新的基因技术正在对它们的“罪行”提出质疑。基因敲除实验表明,许多蛋白是基于间接证据被错误定罪的,只是在错误的时间出现在了错误的地点。