Silke John, Vaux David L
The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia; Department of Medical Biology, University of Melbourne, Parkville, Victoria 3050, Australia.
Semin Cell Dev Biol. 2015 Mar;39:97-105. doi: 10.1016/j.semcdb.2014.12.004. Epub 2014 Dec 26.
Gene deletion studies have helped reveal the unique and overlapping roles played by IAP proteins. Crossing IAP mutant mice has helped unravel the complex feed-back regulatory circuits in which cIAP1, cIAP2 and XIAP allow innate defensive responses to microbial pathogens, without the development of auto-inflammatory syndromes. Deletion of genes for Survivin and its homologs in yeasts, invertebrates and mammals has shown that it functions differently, as it is not a regulator of innate immunity or apoptosis, but acts together with INCENP, aurora kinase B and Borealin to allow chromosome segregation during mitosis.
基因缺失研究有助于揭示IAP蛋白所发挥的独特及重叠作用。使IAP突变小鼠杂交有助于阐明复杂的反馈调节回路,其中cIAP1、cIAP2和XIAP可实现对微生物病原体的先天性防御反应,而不会引发自身炎症综合征。在酵母、无无无脊椎动物和哺乳动物中删除Survivin及其同源基因表明,其功能有所不同,因为它不是先天性免疫或细胞凋亡的调节因子,而是与INCENP、极光激酶B和Borealin共同作用,以在有丝分裂期间实现染色体分离。