首页> 外文期刊>Plant and cell physiology >Cryptogein-Induced Cell Cycle Arrest at G(2) Phase is Associated with Inhibition of Cyclin-Dependent Kinases, Suppression of Expression of Cell Cycle-Related Genes and Protein Degradation in Synchronized Tobacco BY-2 Cells
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Cryptogein-Induced Cell Cycle Arrest at G(2) Phase is Associated with Inhibition of Cyclin-Dependent Kinases, Suppression of Expression of Cell Cycle-Related Genes and Protein Degradation in Synchronized Tobacco BY-2 Cells

机译:在G(2)期Cryptogein诱导的细胞周期阻滞与细胞周期蛋白依赖性激酶的抑制,细胞周期相关基因表达的抑制和同步烟草BY-2细胞蛋白降解相关。

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摘要

Induction of defense responses by pathogens or elicitors is often accompanied by growth inhibition in planta, but its molecular mechanisms are poorly understood. In this report, we characterized the molecular events that occur during cryptogein-induced cell cycle arrest at G(2) phase in synchronously cultured tobacco Bright Yellow-2 (BY-2) cells. Concomitant with the proteinaceous elicitor-induced G(2) arrest, we observed inhibition of the histone H1 kinase activity of cyclin-dependent kinases (CDKs), which correlated with a decrease in mRNA and protein levels of CDKB1. In contrast, the amount of CDKA was almost unaffected by cryptogein even at M phase. Cryptogein rapidly inhibited the expression not only of positive, e.g. A- and B-type cyclins and NtCAK, but also of negative cell cycle regulators such as WEE1, suggesting that cryptogein affects multiple targets to inactivate CDKA to induce G(2) arrest by mechanisms distinct from known checkpoint regulation. Moreover, we show that CDKB1 and cyclin proteins are also rapidly degraded by cryptogein and that the proteasome-dependent protein degradation has a crucial role in the control of cryptogein-induced hypersensitive cell death.
机译:病原体或激发子诱导防御反应通常伴随植物中的生长抑制,但对其分子机制了解甚少。在此报告中,我们表征了在同步培养的烟草Bright Yellow-2(BY-2)细胞中在G(2)阶段由隐壁蛋白诱导的细胞周期停滞期间发生的分子事件。与蛋白质引发剂诱导的G(2)逮捕,我们观察到细胞周期蛋白依赖性激酶(CDKs)的组蛋白H1激酶活性的抑制,这与CDKB1的mRNA和蛋白质水平的降低有关。相反,即使在M期,CDKA的量几乎不受密码素的影响。隐gegegein不仅迅速抑制了阳性表达,例如抑制了其表达。 A型和B型细胞周期蛋白和NtCAK,以及负细胞周期调节剂(例如WEE1),表明隐血球蛋白影响多个目标,以通过不同于已知检查点调节的机制使CDKA失活以诱导G(2)阻滞。此外,我们显示CDKB1和细胞周期蛋白也被隐蛋白快速降解,并且蛋白酶体依赖性蛋白降解在控制隐蛋白诱导的超敏细胞死亡中具有关键作用。

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