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鉴定粗糙脉孢菌中响应渗透胁迫、抗真菌剂咯菌腈和热激诱导的OS-2丝裂原活化蛋白激酶依赖性基因。

Identification of OS-2 MAP kinase-dependent genes induced in response to osmotic stress, antifungal agent fludioxonil, and heat shock in Neurospora crassa.

作者信息

Noguchi Rieko, Banno Shinpei, Ichikawa Ryota, Fukumori Fumiyasu, Ichiishi Akihiko, Kimura Makoto, Yamaguchi Isamu, Fujimura Makoto

机构信息

Faculty of Life Sciences, Toyo University, Itakura, Oura-Gun, Gunma, Japan.

出版信息

Fungal Genet Biol. 2007 Mar;44(3):208-18. doi: 10.1016/j.fgb.2006.08.003. Epub 2006 Sep 20.

Abstract

Two-component signal transduction comprising of OS-1 (histidine kinase), OS-4 (MAPKK kinase), OS-5 (MAPK kinase), and OS-2 (MAP kinase) plays an important role in osmotic regulation in Neurospora crassa. To identify the genes regulated downstream of OS-2 MAP kinase, quantitative real-time RT-PCR analysis was conducted in selected genes based on Hog1 MAP kinase regulated genes in yeast. In response to osmotic stress and fludioxonil, expression of six genes that for glycerol synthesis (gcy-1, gcy-3, and dak-1), gluconeogenesis (fbp-1 and pck-1), and catalase (ctt-1) was activated in the wild-type strain, but not in the os-2 mutant. A heat shock treatment also induced their expression in the same way. Consisting with the gene expression, the enzyme activity of glycerol dehydrogenase, but not glycerol-3-phosphate dehydrogenase, was increased in response to osmotic stress and fludioxonil in the wild-type strain. OS-2 was phosphorylated by the OS-1 cascade in response to relatively low osmotic stress and fludioxonil. However, OS-2 phosphorylation by heat shock and a higher osmotic stress was found in the os-1 mutant normally but not in the os-4 and os-5 mutants. These results suggested that non-OS-1 signaling activates OS-2 in an OS-4-dependent manner in such conditions.

摘要

由OS-1(组氨酸激酶)、OS-4(MAPKK激酶)、OS-5(MAPK激酶)和OS-2(MAP激酶)组成的双组分信号转导在粗糙脉孢菌的渗透调节中起重要作用。为了鉴定OS-2 MAP激酶下游调控的基因,基于酵母中Hog1 MAP激酶调控的基因,对选定的基因进行了定量实时RT-PCR分析。响应渗透胁迫和咯菌腈,野生型菌株中六个参与甘油合成(gcy-1、gcy-3和dak-1)、糖异生(fbp-1和pck-1)以及过氧化氢酶(ctt-1)的基因表达被激活,但在os-2突变体中未被激活。热休克处理也以同样的方式诱导了它们的表达。与基因表达一致,野生型菌株中,响应渗透胁迫和咯菌腈,甘油脱氢酶的酶活性增加,而甘油-3-磷酸脱氢酶的酶活性未增加。响应相对较低的渗透胁迫和咯菌腈,OS-2被OS-1级联磷酸化。然而,在os-1突变体中,热休克和较高渗透胁迫下能正常发现OS-2磷酸化,而在os-4和os-5突变体中则未发现。这些结果表明,在这些条件下,非OS-1信号以OS-4依赖的方式激活OS-2。

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