Galvin Brendan D, Kim Saechin, Horvitz H Robert
Department of Biology, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Genetics. 2008 May;179(1):403-17. doi: 10.1534/genetics.108.087221. Epub 2008 May 5.
Two types of cell death have been studied extensively in Caenorhabditis elegans, programmed cell death and necrosis. We describe a novel type of cell death that occurs in animals containing mutations in either of two genes, lin-24 and lin-33. Gain-of-function mutations in lin-24 and lin-33 cause the inappropriate deaths of many of the Pn.p hypodermal blast cells and prevent the surviving Pn.p cells from expressing their normal developmental fates. The abnormal Pn.p cells in lin-24 and lin-33 mutant animals are morphologically distinct from the dying cells characteristic of C. elegans programmed cell deaths and necrotic cell deaths. lin-24 encodes a protein with homology to bacterial toxins. lin-33 encodes a novel protein. The cytotoxicity caused by mutation of either gene requires the function of the other. An evolutionarily conserved set of genes required for the efficient engulfment and removal of both apoptotic and necrotic cell corpses is required for the full cell-killing effect of mutant lin-24 and lin-33 genes, suggesting that engulfment promotes these cytotoxic cell deaths.
在秀丽隐杆线虫中,两种类型的细胞死亡已得到广泛研究,即程序性细胞死亡和坏死。我们描述了一种新型细胞死亡,它发生在两种基因(lin - 24和lin - 33)之一发生突变的动物中。lin - 24和lin - 33的功能获得性突变导致许多Pn.p皮下前体细胞不适当死亡,并阻止存活的Pn.p细胞表达其正常发育命运。lin - 24和lin - 33突变动物中的异常Pn.p细胞在形态上不同于秀丽隐杆线虫程序性细胞死亡和坏死性细胞死亡所特有的垂死细胞。lin - 24编码一种与细菌毒素具有同源性的蛋白质。lin - 33编码一种新型蛋白质。任一基因的突变所引起的细胞毒性都需要另一个基因的功能。突变的lin - 24和lin - 33基因产生完全的细胞杀伤效应需要一组在进化上保守的基因,这些基因对于有效吞噬和清除凋亡及坏死细胞尸体是必需的,这表明吞噬作用促进了这些细胞毒性细胞死亡。