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秀丽隐杆线虫的MAC-1是ATP酶AAA家族的一个必需成员,它可以结合CED-4并阻止细胞死亡。

C. elegans MAC-1, an essential member of the AAA family of ATPases, can bind CED-4 and prevent cell death.

作者信息

Wu D, Chen P J, Chen S, Hu Y, Nuñez G, Ellis R E

机构信息

Department of Pathology and Comprehensive Cancer Center, University of Michigan Medical School, The University of Michigan, Ann Arbor, Michigan 48109, USA.

出版信息

Development. 1999 May;126(9):2021-31. doi: 10.1242/dev.126.9.2021.

Abstract

In the nematode Caenorhabditis elegans, CED-4 plays a central role in the regulation of programmed cell death. To identify proteins with essential or pleiotropic activities that might also regulate cell death, we used the yeast two-hybrid system to screen for CED-4-binding proteins. We identified MAC-1, a member of the AAA family of ATPases that is similar to Smallminded of Drosophila. Immunoprecipitation studies confirm that MAC-1 interacts with CED-4, and also with Apaf-1, the mammalian homologue of CED-4. Furthermore, MAC-1 can form a multi-protein complex that also includes CED-3 or CED-9. A MAC-1 transgene under the control of a heat shock promoter prevents some natural cell deaths in C. elegans, and this protection is enhanced in a ced-9(n1950sd)/+ genetic background. We observe a similar effect in mammalian cells, where expression of MAC-1 can prevent CED-4 and CED-3 from inducing apoptosis. Finally, mac-1 is an essential gene, since inactivation by RNA-mediated interference causes worms to arrest early in larval development. This arrest is similar to that observed in Smallminded mutants, but is not related to the ability of MAC-1 to bind CED-4, since it still occurs in ced-3 or ced-4 null mutants. These results suggest that MAC-1 identifies a new class of proteins that are essential for development, and which might regulate cell death in specific circumstances.

摘要

在秀丽隐杆线虫中,CED - 4在程序性细胞死亡的调控中起核心作用。为了鉴定可能也调控细胞死亡的具有重要或多效性活性的蛋白质,我们利用酵母双杂交系统筛选与CED - 4结合的蛋白质。我们鉴定出MAC - 1,它是AAA型ATP酶家族的成员,与果蝇的Smallminded相似。免疫沉淀研究证实MAC - 1与CED - 4相互作用,也与CED - 4的哺乳动物同源物Apaf - 1相互作用。此外,MAC - 1能形成一个还包括CED - 3或CED - 9的多蛋白复合物。在热休克启动子控制下的MAC - 1转基因可防止秀丽隐杆线虫中的一些自然细胞死亡,并且在ced - 9(n1950sd)/+遗传背景下这种保护作用增强。我们在哺乳动物细胞中观察到类似的效应,其中MAC - 1的表达可防止CED - 4和CED - 3诱导细胞凋亡。最后,mac - 1是一个必需基因,因为RNA介导的干扰使其失活会导致线虫在幼虫发育早期停滞。这种停滞类似于在Smallminded突变体中观察到的情况,但与MAC - 1结合CED - 4的能力无关,因为它在ced - 3或ced - 4缺失突变体中仍然发生。这些结果表明MAC - 1鉴定出了一类对发育至关重要且可能在特定情况下调控细胞死亡的新蛋白质。

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