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通过比较 S. pombe 和 S. cerevisiae 的遗传相互作用揭示功能重用途。

Functional repurposing revealed by comparing S. pombe and S. cerevisiae genetic interactions.

机构信息

Department of Biochemistry, Huntsman Cancer Institute, University of Utah, School of Medicine, Salt Lake City, 84112, USA.

出版信息

Cell. 2012 Jun 8;149(6):1339-52. doi: 10.1016/j.cell.2012.04.028.

Abstract

We present a genetic interaction map of pairwise measures including ∼40% of nonessential S. pombe genes. By comparing interaction maps for fission and budding yeast, we confirmed widespread conservation of genetic relationships within and between complexes and pathways. However, we identified an important subset of orthologous complexes that have undergone functional "repurposing": the evolution of divergent functions and partnerships. We validated three functional repurposing events in S. pombe and mammalian cells and discovered that (1) two lumenal sensors of misfolded ER proteins, the kinase/nuclease Ire1 and the glucosyltransferase Gpt1, act together to mount an ER stress response; (2) ESCRT factors regulate spindle-pole-body duplication; and (3) a membrane-protein phosphatase and kinase complex, the STRIPAK complex, bridges the cis-Golgi, the centrosome, and the outer nuclear membrane to direct mitotic progression. Each discovery opens new areas of inquiry and-together-have implications for model organism-based research and the evolution of genetic systems.

摘要

我们呈现了一个包括大约 40%非必需 S. pombe 基因的成对测量的遗传相互作用图谱。通过比较裂殖酵母和芽殖酵母的相互作用图谱,我们确认了在复合物和途径内和之间遗传关系的广泛保守性。然而,我们确定了一个重要的同源复合物子集,这些复合物经历了功能“重新定位”:功能和伙伴关系的分歧进化。我们在 S. pombe 和哺乳动物细胞中验证了三个功能重新定位事件,并发现 (1) 两种错误折叠内质网蛋白的腔传感器,激酶/核酸内切酶 Ire1 和葡萄糖基转移酶 Gpt1,共同作用以引发内质网应激反应;(2) ESCRT 因子调节纺锤体极体复制;以及 (3) 一种膜蛋白磷酸酶和激酶复合物,STRIPAK 复合物,连接顺式高尔基体、中心体和外核膜,以指导有丝分裂进程。每一个发现都开辟了新的研究领域,并且——共同——对基于模式生物的研究和遗传系统的进化具有影响。

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