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PKA 依赖性调控芽殖酵母中 Cdc25 RasGEF 的定位。

PKA-dependent regulation of Cdc25 RasGEF localization in budding yeast.

机构信息

Department of Biotechnology and Biosciences, University of Milano-Bicocca, Milan, Italy.

出版信息

FEBS Lett. 2011 Dec 15;585(24):3914-20. doi: 10.1016/j.febslet.2011.10.032. Epub 2011 Oct 25.

Abstract

In Saccharomyces cerevisiae the Cdc25/Ras/cAMP pathway is involved in cell growth and proliferation regulation. Ras proteins are regulated by Ira1/2 GTPase activating proteins (GAPs) and Cdc25/Sdc25 guanine nucleotide exchange factors (GEFs). Most of cytosolic Cdc25 protein was found on internal membranes in exponentially growing cells, while upon incubation in a buffer with no nutrients it is re-localized to plasma membrane. The overexpression of Tpk1 PKA catalytic subunit also induces Cdc25 export from the nucleus, involving two serine residues near the Nuclear Localization Site (NLS): mutation of Ser(825) and Ser(826) to glutamate is sufficient to exclude physiologically expressed Cdc25 from the nucleus, mimicking Tpk1 overproduction effect. Mutation of these Ser residues to Ala abolishes the effect of nuclear export induced by Tpk1 overexpression on a Cdc25eGFP fusion. Moreover, mutation of these residues affects PKA-related phenotypes such as heat shock resistance, glycogen content and cell volume.

摘要

在酿酒酵母中,CDC25/Ras/cAMP 途径参与细胞生长和增殖的调节。Ras 蛋白受 Ira1/2 GTP 酶激活蛋白(GAPs)和 CDC25/Sdc25 鸟嘌呤核苷酸交换因子(GEFs)调节。在指数生长期的细胞中,大多数细胞质 CDC25 蛋白位于内膜上,而在没有营养物质的缓冲液中孵育时,它被重新定位到质膜上。TPK1 PKA 催化亚基的过表达也会诱导 CDC25 从核内输出,涉及核定位信号(NLS)附近的两个丝氨酸残基:Ser(825)和 Ser(826)突变为谷氨酸足以将生理表达的 CDC25 排除在核外,模拟 TPK1 过表达的效果。将这些 Ser 残基突变为 Ala 会消除 Tpk1 过表达对 Cdc25eGFP 融合物诱导的核输出的影响。此外,这些残基的突变会影响与 PKA 相关的表型,如热休克抗性、糖原含量和细胞体积。

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