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首页> 外文期刊>Apoptosis >The murine cytomegalovirus cell death suppressor m38.5 binds Bax and blocks Bax-mediated mitochondrial outer membrane permeabilization
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The murine cytomegalovirus cell death suppressor m38.5 binds Bax and blocks Bax-mediated mitochondrial outer membrane permeabilization

机译:小鼠巨细胞病毒细胞死亡抑制剂m38.5结合Bax并阻断Bax介导的线粒体外膜通透性

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Apoptosis is increasingly implicated as an early line of defense against viral infections. Viruses have devised numerous strategies to delay apoptosis of infected cells. Many viruses encode cell death suppressors that target mitochondrial apoptotic signaling pathway, indicating the importance of this pathway in the anti-viral response. Human and primate cytomegaloviruses encode the viral mitochondria-localized inhibitor of apoptosis vMIA, but no overt homologue of vMIA was identified in any non-primate cytomegalovirus. Here we report that m38.5 protein encoded by murine cytomegalovirus, which is unrelated to vMIA in its amino acid sequence, delays death receptor ligation-induced cell death, and that m38.5 associates with Bax, recruits it to mitochondria, and blocks Bax-mediated but not Bak-mediated mitochondrial outer membrane permeabilization. Thus, primate and murine cytomegaloviruses have evolved non-homologous but functionally similar cell death suppressors selectively targeting the Bax-mediated branch of the mitochondrial apoptotic signaling pathway, indicating the importance of this branch in the response of diverse host organisms against cytomegalovirus infections.
机译:凋亡越来越多地被认为是抵抗病毒感染的早期防线。病毒已经设计出许多策略来延迟被感染细胞的凋亡。许多病毒编码靶向线粒体凋亡信号通路的细胞死亡抑制剂,表明该通路在抗病毒反应中的重要性。人和灵长类巨细胞病毒编码病毒线粒体定位的凋亡vMIA抑制剂,但在任何非灵长类巨细胞病毒中均未发现vMIA的明显同源性。在这里,我们报道鼠巨细胞病毒编码的m38.5蛋白与vMIA的氨基酸序列无关,延迟了死亡受体连接诱导的细胞死亡,并且m38.5与Bax结合,将其募集到线粒体并阻断Bax介导但不是Bak介导的线粒体外膜通透性。因此,灵长类和鼠类巨细胞病毒已经进化出非同源但功能相似的细胞死亡抑制剂,选择性靶向线粒体凋亡信号通路的Bax介导的分支,表明该分支在多种宿主生物对巨细胞病毒感染的反应中的重要性。

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