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参与酵母中合适生长位点选择的Rsr1/Bud1 GTP酶的定位

Localization of the Rsr1/Bud1 GTPase involved in selection of a proper growth site in yeast.

作者信息

Park Hay-Oak, Kang Pil Jung, Rachfal Amy Wilson

机构信息

Graduate Program in Molecular, Cellular, and Developmental Biology, Department of Molecular Genetics, The Ohio State University, 484 West 12th Avenue, Columbus, OH 43210-1292, USA.

出版信息

J Biol Chem. 2002 Jul 26;277(30):26721-4. doi: 10.1074/jbc.C200245200. Epub 2002 Jun 10.

Abstract

Yeast cells organize their actin cytoskeleton in a highly polarized manner during vegetative growth. The Ras-like GTPase Rsr1/Bud1 and its regulators are required for selection of a specific site for growth. Here we showed that Rsr1/Bud1 was broadly distributed on the plasma membrane and highly concentrated at the incipient bud site and polarized growth sites. We also showed that localization of Cdc24, a guanine nucleotide exchange factor for the Cdc42 GTPase, to the proper bud site was dependent on Rsr1/Bud1. Surprisingly, Rsr1/Bud1 also localized to intracellular membranes. A mutation in the lysine repeat in the hypervariable region of Rsr1/Bud1 specifically abolished its plasma membrane localization, whereas a mutation at the CAAX motif eliminated both plasma membrane and internal membrane association of Rsr1/Bud1. Thus the lysine repeat and the CAAX motif of Rsr1/Bud1 are important for its localization to the plasma membrane and to the polarized growth sites. This localization of Rsr1/Bud1 is essential for its function in proper bud site selection because both mutations resulted in random bud site selection.

摘要

酵母细胞在营养生长过程中以高度极化的方式组织其肌动蛋白细胞骨架。类Ras GTP酶Rsr1/Bud1及其调节因子是选择特定生长位点所必需的。在这里,我们表明Rsr1/Bud1广泛分布在质膜上,并高度集中在初始芽位点和极化生长位点。我们还表明,Cdc42 GTP酶的鸟嘌呤核苷酸交换因子Cdc24定位于合适的芽位点依赖于Rsr1/Bud1。令人惊讶的是,Rsr1/Bud1也定位于内膜。Rsr1/Bud1高变区赖氨酸重复序列中的一个突变特异性地消除了其质膜定位,而CAAX基序处的一个突变则消除了Rsr1/Bud1与质膜和内膜的结合。因此,Rsr1/Bud1的赖氨酸重复序列和CAAX基序对于其定位于质膜和极化生长位点很重要。Rsr1/Bud1的这种定位对于其在正确芽位点选择中的功能至关重要,因为这两个突变都导致了随机芽位点选择。

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