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首页> 外文期刊>The Plant Cell >The Ustilago maydis Clp1 Protein Orchestrates Pheromone and b-Dependent Signaling Pathways to Coordinate the Cell Cycle and Pathogenic Development
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The Ustilago maydis Clp1 Protein Orchestrates Pheromone and b-Dependent Signaling Pathways to Coordinate the Cell Cycle and Pathogenic Development

机译:稻草乌贼(Ustilago maydis)Clp1蛋白可协调信息素和b依赖性信号通路来协调细胞周期和致病性发育

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摘要

Regulation of the cell cycle and morphogenetic switching during pathogenic and sexual development in Ustilago maydis is orchestrated by a concerted action of the a and b mating-type loci. Activation of either mating-type locus triggers the G2 cell cycle arrest that is a prerequisite for the formation of the infectious dikaryon; this cell cycle arrest is released only after penetration of the host plant. Here, we show that bW, one of the two homeodomain transcription factors encoded by the b mating-type locus, and the zinc-finger transcription factor Rbf1, a master regulator for pathogenic development, interact with Clp1 (clampless 1), a protein required for the distribution of nuclei during cell division of the dikaryon. In addition, we identify Cib1, a previously undiscovered bZIP transcription factor required for pathogenic development, as a Clp1-interacting protein. Clp1 interaction with bW blocks b-dependent functions, such as the b-dependent G2 cell cycle arrest and dimorphic switching. The interaction of Clp1 with Rbf1 results in the repression of the a-dependent pheromone pathway, conjugation tube formation, and the a-induced G2 cell cycle arrest. The concerted interaction of Clp1 with Rbf1 and bW coordinates a-and b-dependent cell cycle control and ensures cell cycle release and progression at the onset of biotrophic development.
机译:甲型和乙型交配型基因座的协同作用可调控Ustilago致病和性发育过程中细胞周期的调控和形态发生转换。任一个交配型基因座的激活都会触发G2细胞周期停滞,这是形成传染性双核细胞的前提条件。该细胞周期停滞仅在宿主植物穿透后才释放。在这里,我们显示bW(由b交配型基因座编码的两个同源域转录因子之一)和锌指转录因子Rbf1(致病性发育的主要调控因子)与Clp1(无钳位1)相互作用,Clp1(无钳位1)是一种蛋白质双核细胞分裂过程中细胞核的分布。此外,我们将Cib1(与病原体发育相关的先前未发现的bZIP转录因子)识别为Clp1相互作用蛋白。 Clp1与bW的相互作用会阻止b依赖性功能,例如b依赖性G2细胞周期停滞和双态转换。 Clp1与Rbf1的相互作用导致a依赖性信息素途径的抑制,结合管的形成以及a诱导的G2细胞周期停滞。 Clp1与Rbf1和bW的协调相互作用协调了a和b依赖的细胞周期控制,并确保了在生物营养发展开始时细胞周期的释放和进展。

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