首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Complex Haploinsufficiency-Based Genetic Analysis of the NDR/Lats Kinase Cbk1 Provides Insight into Its Multiple Functions in Candida albicans
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Complex Haploinsufficiency-Based Genetic Analysis of the NDR/Lats Kinase Cbk1 Provides Insight into Its Multiple Functions in Candida albicans

机译:基于复杂单倍功能不足的NDR / Lats激酶Cbk1的遗传分析,可了解其在白色念珠菌中的多种功能

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摘要

Although the analysis of genetic interactions and networks is a powerful approach to understanding biology, it has not been applied widely to the pathogenic yeast Candida albicans . Here, we describe the use of both screening and directed genetic interaction studies based on complex haploinsufficiency to probe the function of the R egulation of A ce2 and M orphogenesis (RAM) pathway in C. albicans . A library of 5200 Tn7 -mutagenized derivatives of a parental strain heterozygous at CBK1 , the key kinase in the RAM pathway, was screened for alterations in serum-induced filamentation. Following confirmation of phenotypes and identification of insertion sites by sequencing, a set of 36 unique double heterozygous strains showing complex haploinsufficiency was obtained. In addition to a large set of genes regulated by the RAM transcription factor Ace2, genes related to cell wall biosynthesis, cell cycle, polarity, oxidative stress, and nitrogen utilization were identified. Follow-up analysis led to the first demonstration that the RAM pathway is required for oxidative stress tolerance in a manner related to the two-component-regulated kinase Chk1 and revealed a potential direct connection between the RAM pathway and the essential Mps1 spindle pole-related kinase. In addition, genetic interactions with CDC42 -related genes MSB1 , a putative scaffold protein, and RGD3 , a putative Rho GTPase-activating protein (GAP) were identified. We also provide evidence that Rgd3 is a GAP for Cdc42 and show that its localization and phosphorylation are dependent on Cbk1.
机译:尽管遗传相互作用和网络的分析是了解生物学的有力方法,但尚未广泛应用于致病性酵母白色念珠菌。在这里,我们描述了基于复杂单倍体不足的筛查和定向遗传相互作用研究,以探测白色念珠菌中A ce2和M造血(RAM)途径的调控功能。筛选了5200个Tn7突变的CBK1杂合子的亲本菌株衍生物,该文库是RAM途径中的关键激酶,用于血清诱导的丝化过程中的变化。在确认表型并通过测序鉴定插入位点后,获得了一组显示复杂单倍体不足的36个独特的双杂合菌株。除了由RAM转录因子Ace2调控的大量基因外,还鉴定了与细胞壁生物合成,细胞周期,极性,氧化应激和氮利用相关的基因。后续分析得出了第一个证明,即氧化应激耐受性需要RAM途径,该途径与双组分调节激酶Chk1有关,并揭示了RAM途径与必需的Mps1纺锤极相关的潜在直接联系。激酶。此外,鉴定了与CDC42相关基因MSB1,推定的支架蛋白和RGD3,推定的Rho GTPase激活蛋白(GAP)的遗传相互作用。我们还提供证据表明Rgd3是Cdc42的GAP,并表明其定位和磷酸化取决于Cbk1。

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