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通过功能基因组学剖析复杂表型揭示了酵母细胞周期蛋白依赖性蛋白激酶Pho85在应激适应和细胞完整性中的作用。

Dissection of a complex phenotype by functional genomics reveals roles for the yeast cyclin-dependent protein kinase Pho85 in stress adaptation and cell integrity.

作者信息

Huang Dongqing, Moffat Jason, Andrews Brenda

机构信息

Department of Medical Genetics and Microbiology, University of Toronto, Toronto, Ontario, Canada M5S 1A8.

出版信息

Mol Cell Biol. 2002 Jul;22(14):5076-88. doi: 10.1128/MCB.22.14.5076-5088.2002.

Abstract

Cyclin-dependent kinases (Cdks) are key regulators of the cell division cycle. Pho85 is a multifunctional Cdk in budding yeast involved in aspects of metabolism, the cell cycle, cell polarity, and gene expression. Consistent with a broad spectrum of functions, Pho85 associates with a family of 10 cyclins and deletion of PHO85 causes a pleiotropic phenotype. Discovering the physiological substrates of protein kinases is a major challenge, and we have pursued a number of genomics approaches to reveal the processes regulated by Pho85 and to understand the root cause of reduced cellular fitness in pho85Delta mutant strains. We used a functional-genomics approach called synthetic genetic array (SGA) analysis to systematically identify strain backgrounds in which PHO85 is required for viability. In parallel, we used DNA microarrays to examine the genome-wide transcriptional consequences of deleting PHO85 or members of the Pho85 cyclin family. Using this pairwise approach coupled with phenotypic tests, we uncovered clear roles for Pho85 in cell integrity and the response to adverse growth conditions. Importantly, our combined approach allowed us to ascribe new aspects of the complex pho85 phenotype to particular cyclins; our data highlight a cell integrity function for the Pcl1,2 subgroup of Pho85 Cdks that is independent of a role for the Pho80-Pho85 kinase in the response to stress. Using a modification of the SGA technique to screen for suppressors of pho85Delta strain growth defects, we found that deletion of putative vacuole protein gene VTC4 suppressed the sensitivity of the pho85Delta strain to elevated CaCl(2) and many other stress conditions. Expression of VTC4 is regulated by Pho4, a transcription factor that is inhibited by the Pho80-Pho85 kinase. Genetic tests and electron microscopy experiments suggest that VTC4 is a key target of Pho4 and that Pho80-Pho85-mediated regulation of VTC4 expression is required for proper vacuole function and for yeast cell survival under a variety of suboptimal conditions. The integration of multiple genomics approaches is likely to be a generally useful strategy for extracting functional information from pleiotropic mutant phenotypes.

摘要

细胞周期蛋白依赖性激酶(Cdks)是细胞分裂周期的关键调节因子。Pho85是芽殖酵母中的一种多功能Cdk,参与代谢、细胞周期、细胞极性和基因表达等多个方面。与广泛的功能一致,Pho85与10种细胞周期蛋白家族成员相关联,PHO85的缺失会导致多效性表型。发现蛋白激酶的生理底物是一项重大挑战,我们采用了多种基因组学方法来揭示由Pho85调节的过程,并了解pho85Delta突变菌株细胞适应性降低的根本原因。我们使用了一种称为合成遗传阵列(SGA)分析的功能基因组学方法,系统地鉴定PHO85对生存力至关重要的菌株背景。同时,我们使用DNA微阵列来检查删除PHO85或Pho85细胞周期蛋白家族成员后的全基因组转录后果。通过这种成对方法结合表型测试,我们发现Pho85在细胞完整性和对不利生长条件的反应中具有明确作用。重要的是,我们的联合方法使我们能够将复杂的pho85表型的新方面归因于特定的细胞周期蛋白;我们的数据突出了Pho85 Cdk的Pcl1,2亚组在细胞完整性方面的功能,该功能独立于Pho80-Pho85激酶在应激反应中的作用。通过对SGA技术进行改进以筛选pho85Delta菌株生长缺陷的抑制因子,我们发现假定的液泡蛋白基因VTC4的缺失抑制了pho85Delta菌株对升高的CaCl2和许多其他应激条件的敏感性。VTC4的表达受Pho4调节,Pho4是一种受Pho80-Pho85激酶抑制的转录因子。遗传测试和电子显微镜实验表明,VTC4是Pho4的关键靶点,Pho80-Pho85介导的VTC4表达调控对于液泡的正常功能以及酵母细胞在各种次优条件下的存活是必需的。整合多种基因组学方法可能是从多效性突变体表型中提取功能信息的一种普遍有用的策略。

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