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Cdk8 调节转录因子 Phd1 的稳定性,以控制酿酒酵母的假菌丝分化。

Cdk8 regulates stability of the transcription factor Phd1 to control pseudohyphal differentiation of Saccharomyces cerevisiae.

机构信息

Department of Biochemistry and Molecular Biology, Molecular Epigenetics, LSI, University of British Columbia, Vancouver, British Columbia, Canada.

出版信息

Mol Cell Biol. 2012 Feb;32(3):664-74. doi: 10.1128/MCB.05420-11. Epub 2011 Nov 28.

Abstract

The yeast Saccharomyces differentiates into filamentous pseudohyphae when exposed to a poor source of nitrogen in a process involving a collection of transcription factors regulated by nutrient signaling pathways. Phd1 is important for this process in that it regulates expression of most other transcription factors involved in differentiation and can induce filamentation on its own when overproduced. In this article, we show that Phd1 is an unstable protein whose degradation is initiated through phosphorylation by Cdk8 of the RNA polymerase II mediator subcomplex. Phd1 is stabilized by cdk8 disruption, and the naturally filamenting Σ1278b strain was found to have a sequence polymorphism that eliminates a Cdk8 phosphorylation site, which both stabilizes the protein and contributes to enhanced differentiation. In nitrogen-starved cells, PHD1 expression is upregulated and the Phd1 protein becomes stabilized, which causes its accumulation during differentiation. PHD1 expression is partially dependent upon Ste12, which was also previously shown to be destabilized by Cdk8-dependent phosphorylations, but to a significantly smaller extent than Phd1. These observations demonstrate the central role that Cdk8 plays in initiation of differentiation. Cdk8 activity is inhibited in cells shifted to limiting nutrient conditions, and we argue that this effect drives the initiation of differentiation through stabilization of multiple transcription factors, including Phd1, that cause activation of genes necessary for filamentous response.

摘要

酵母 Saccharomyces 在暴露于氮源不足的环境中时会分化为丝状假菌丝,这一过程涉及一系列转录因子的集合,这些转录因子受营养信号通路调控。Phd1 在此过程中非常重要,因为它调节大多数其他参与分化的转录因子的表达,并且在过量产生时可以自行诱导丝状生长。在本文中,我们表明 Phd1 是一种不稳定的蛋白质,其降解是通过 RNA 聚合酶 II 介导亚基复合物的 Cdk8 磷酸化启动的。Phd1 通过 cdk8 破坏而稳定,并且发现自然丝状的 Σ1278b 菌株存在消除 Cdk8 磷酸化位点的序列多态性,这既稳定了蛋白质,又促进了分化。在氮饥饿的细胞中,PHD1 的表达上调,Phd1 蛋白变得稳定,这导致其在分化过程中的积累。PHD1 的表达部分依赖于 Ste12,Ste12 先前也被证明是由 Cdk8 依赖性磷酸化所不稳定的,但程度明显小于 Phd1。这些观察结果表明 Cdk8 在起始分化中起着核心作用。当细胞转移到限制营养条件下时,Cdk8 的活性受到抑制,我们认为这种效应通过稳定多个转录因子(包括 Phd1)来启动分化,这些转录因子导致丝状反应所需基因的激活。

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