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Its8是Mcd4和Pig-n的裂殖酵母同源物,参与糖基磷脂酰肌醇(GPI)锚的合成,并在胞质分裂中与钙调神经磷酸酶具有重要功能。

Its8, a fission yeast homolog of Mcd4 and Pig-n, is involved in GPI anchor synthesis and shares an essential function with calcineurin in cytokinesis.

作者信息

Yada T, Sugiura R, Kita A, Itoh Y, Lu Y, Hong Y, Kinoshita T, Shuntoh H, Kuno T

机构信息

Department of Pharmacology, Kobe University School of Medicine, Kobe 650-0017, Japan.

出版信息

J Biol Chem. 2001 Apr 27;276(17):13579-86. doi: 10.1074/jbc.M009260200. Epub 2001 Jan 31.

Abstract

In fission yeast, calcineurin is required for cytokinesis and ion homeostasis; however, most of its physiological roles remain obscure. To identify genes that share an essential function with calcineurin, we screened for mutations that confer sensitivity to the calcineurin inhibitor FK506 and high temperature and isolated the mutant its8-1. its8(+) encodes a homolog of the budding yeast MCD4 and human Pig-n that are involved in glycosylphosphatidylinositol (GPI) anchor synthesis. Consistently, reduced inositol labeling of proteins suggested impaired GPI anchor synthesis in its8-1 mutants. The temperature upshift induced a further decrease in inositol labeling and caused dramatic increases in the frequency of septation in its8-1 mutants. BE49385A, an inhibitor of MCD4 and Pig-n, also increased the septation index of the wild-type cell. Osmotic stabilization suppressed these morphological defects, indicating that cell wall weakness caused by impaired GPI anchor synthesis resulted in abnormal cytokinesis. Furthermore, calcineurin-deleted cells exhibited hypersensitivity to BE49385A, and FK506 exacerbated the cytokinesis defects of the its8-1 mutant. Thus, calcineurin and Its8 may share an essential function in cytokinesis and cell viability through the regulation of cell wall integrity.

摘要

在裂殖酵母中,钙调神经磷酸酶对于胞质分裂和离子稳态是必需的;然而,其大多数生理功能仍不清楚。为了鉴定与钙调神经磷酸酶具有共同基本功能的基因,我们筛选了对钙调神经磷酸酶抑制剂FK506和高温敏感的突变体,并分离出了its8-1突变体。its8(+)编码与参与糖基磷脂酰肌醇(GPI)锚合成的芽殖酵母MCD4和人类Pig-n同源的蛋白。一致地,蛋白质的肌醇标记减少表明its8-1突变体中GPI锚合成受损。温度升高导致its8-1突变体中肌醇标记进一步减少,并导致隔膜形成频率显著增加。BE49385A是MCD4和Pig-n的抑制剂,它也增加了野生型细胞的隔膜指数。渗透稳定作用抑制了这些形态缺陷,表明GPI锚合成受损导致的细胞壁脆弱导致了异常的胞质分裂。此外,缺失钙调神经磷酸酶的细胞对BE49385A表现出超敏反应,FK506加剧了its8-1突变体的胞质分裂缺陷。因此,钙调神经磷酸酶和Its8可能通过调节细胞壁完整性在胞质分裂和细胞活力中共享基本功能。

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