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鉴定影响粟酒裂殖酵母有丝分裂到间期转变的cDNA,包括编码spi1p-GTP结合蛋白的sbp1。

The identification of cDNAs that affect the mitosis-to-interphase transition in Schizosaccharomyces pombe, including sbp1, which encodes a spi1p-GTP-binding protein.

作者信息

He X, Hayashi N, Walcott N G, Azuma Y, Patterson T E, Bischoff F R, Nishimoto T, Sazer S

机构信息

Verna and Marrs McLean Department of Biochemistry, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Genetics. 1998 Feb;148(2):645-56. doi: 10.1093/genetics/148.2.645.

Abstract

Perturbations of the spi1p GTPase system in fission yeast, caused by mutation or overexpression of several regulatory proteins, result in a unique terminal phenotype that includes condensed chromosomes, a wide medial septum, and a fragmented nuclear envelope. To identify potential regulators or targets of the spi1p GTPase system, a screen for cDNAs whose overexpression results in this terminal phenotype was conducted, and seven clones that represent three genes, named med1, med2, and med3 (mitotic exit defect), were identified. Their genetic interaction with the spi1p GTPase system was established by showing that the spi1p guanine nucleotide exchange factor mutant pim1-d1ts was hypersensitive to their overexpression. med1 encodes a homologue of the human Ran-binding protein, RanBP1, and has been renamed sbp1 (spi1-binding protein). sbp1p binds to spi1p-GTP and costimulates the GTPase-activating protein (GAP)-catalyzed GTPase activity. Cells in which sbp1p is depleted or overproduced phenocopy cells in which the balance between spi1p-GTP and spi1p-GDP is perturbed by other means. Therefore, sbp1p mediates and/or regulates the essential functions of the spi1p GTPase system. med2 and med3 encode novel fission yeast proteins that, based on our phenotypic analyses, are likely to identify additional regulators or effectors of the spi1p GTPase system.

摘要

裂殖酵母中spi1p GTP酶系统的扰动,由几种调节蛋白的突变或过表达引起,会导致一种独特的终末表型,包括染色体浓缩、宽的中间隔膜和破碎的核膜。为了鉴定spi1p GTP酶系统的潜在调节因子或靶点,我们进行了一项筛选,寻找过表达会导致这种终末表型的cDNA,结果鉴定出了七个代表三个基因的克隆,分别命名为med1、med2和med3(有丝分裂退出缺陷)。通过证明spi1p鸟嘌呤核苷酸交换因子突变体pim1-d1ts对它们的过表达高度敏感,确定了它们与spi1p GTP酶系统的遗传相互作用。med1编码人类Ran结合蛋白RanBP1的同源物,现已重新命名为sbp1(spi1结合蛋白)。sbp1p与spi1p-GTP结合,并协同刺激GTP酶激活蛋白(GAP)催化的GTP酶活性。sbp1p缺失或过量产生的细胞,其表型类似于通过其他方式扰乱spi1p-GTP和spi1p-GDP平衡的细胞。因此,sbp1p介导和/或调节spi1p GTP酶系统的基本功能。med2和med3编码新型裂殖酵母蛋白,根据我们的表型分析,它们可能会鉴定出spi1p GTP酶系统的其他调节因子或效应器。

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