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Protein Kinases Involved in Mating and Osmotic Stress in the Yeast Kluyveromyces lactis

机译:蛋白激酶参与酵母克鲁维酵母的交配和渗透压。

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Systematic disruption of genes encoding kinases and mitogen-activated protein kinases (MAPKs) was performed in Kluyveromyces lactis haploid cells. The mutated strains were assayed by their capacity to mate and to respond to hyperosmotic stress. The K. lactis Ste11p (KlSte11p) MAPK kinase kinase (MAPKKK) was found to act in both mating and osmoresponse pathways while the scaffold KlSte5p and the MAPK KlFus3p appeared to be specific for mating. The p21-activated kinase KlSte20p and the kinase KlSte50p participated in both pathways. Protein association experiments showed interaction of KlSte50p and KlSte20p with Gα and Gβ, respectively, the G protein subunits involved in the mating pathway. Both KlSte50p and KlSte20p also showed interaction with KlSte11p. Disruption mutants of the K. lactis PBS2 (KlPBS2) and KlHOG1 genes of the canonical osmotic response pathway resulted in mutations sensitive to high salt and high sorbitol but dispensable for mating. Mutations that eliminate the MAPKK KlSte7p activity had a strong effect on mating and also showed sensitivity to osmotic stress. Finally, we found evidence of physical interaction between KlSte7p and KlHog1p, in addition to diminished Hog1p phosphorylation after a hyperosmotic shock in cells lacking KlSte7p. This study reveals novel roles for components of transduction systems in yeast.
机译:在乳酸克鲁维酵母单倍体细胞中对编码激酶和有丝分裂原活化蛋白激酶(MAPK)的基因进行了系统破坏。通过突变菌株的交配和对高渗胁迫的反应能力对其进行了分析。 K。乳酸Ste11p(KlSte11p)MAPK激酶激酶(MAPKKK)在交配和渗透反应途径中均起作用,而支架KlSte5p和MAPK KlFus3p似乎对交配具有特异性。 p21激活的激酶KlSte20p和激酶KlSte50p参与了这两个途径。蛋白质缔合实验显示,KlSte50p和KlSte20p分别与Gα和Gβ(参与交配途径的G蛋白亚基)相互作用。 KlSte50p和KlSte20p都显示出与KlSte11p的相互作用。 K的破坏突变体。典型的渗透反应途径的乳酸PBS2 (Kl PBS2 )和Kl HOG1 基因导致对高盐和高山梨醇敏感的突变,但可交配。消除MAPKK KlSte7p活性的突变对交配有很强的影响,并且还表现出对渗透胁迫的敏感性。最后,我们发现缺乏KlSte7p的细胞发生高渗休克后,除了减少了Hog1p的磷酸化外,KlSte7p和KlHog1p之间存在物理相互作用的证据。这项研究揭示了酵母中转导系统组件的新作用。

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