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Mating and Pathogenic Development of the Smut Fungus Ustilago maydis Are Regulated by One Mitogen-Activated Protein Kinase Cascade

机译:黑穗病菌Utilago maydis的交配和致病性发育受一种丝裂原活化的蛋白激酶级联的调节。

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In the phytopathogenic fungus Ustilago maydis, pheromone-mediated cell fusion is a prerequisite for the generation of the infectious dikaryon. The pheromone signal elevates transcription of the pheromone genes and elicits formation of conjugation hyphae. Cyclic AMP and mitogen-activated protein kinase (MAPK) signaling are involved in this process. The MAPK cascade is presumed to be composed of Ubc4 (MAPK kinase kinase), Fuz7 (MAPK kinase), and Ubc3/Kpp2 (MAPK). We isolated the kpp4 gene and found it to be allelic to ubc4. Epistasis analyses with constitutively active alleles of kpp4 and fuz7 substantiate that Kpp4, Fuz7, and Kpp2/Ubc3 are components of the same module. Moreover, we demonstrate that Fuz7 activates Kpp2 and shows interactions in vitro. Signaling via this cascade regulates expression of pheromone-responsive genes, presumably through acting on the transcription factor Prf1. Interestingly, the same cascade is needed for conjugation tube formation, and this process does not involve Prf1. In addition, fuz7 as well as kpp4 deletion strains are nonpathogenic, while kpp2 deletion mutants are only attenuated in pathogenesis. Here we show that strains expressing the unphosphorylatable allele kpp2T182A/Y184F are severely affected in tumor induction and display defects in early infection-related differentiation.
机译:在植物致病性真菌 Ustilago maydis 中,信息素介导的细胞融合是产生双核传染性的前提。信息素信号提高信息素基因的转录并引发共轭菌丝的形成。循环AMP和有丝分裂原激活的蛋白激酶(MAPK)信号参与此过程。推测MAPK级联由Ubc4(MAPK激酶激酶),Fuz7(MAPK激酶)和Ubc3 / Kpp2(MAPK)组成。我们分离了 kpp4 基因,发现它与 ubc4 等位基因。用 kpp4 fuz7 的组成型活性等位基因进行上位性分析,证明Kpp4,Fuz7和Kpp2 / Ubc3是同一模块的组成部分。此外,我们证明Fuz7激活Kpp2并显示体外相互作用。通过这种级联的信号传导可能通过作用于转录因子Prf1来调节信息素应答基因的表达。有趣的是,共轭管的形成需要相同的级联,并且此过程不涉及Prf1。此外, fuz7 以及 kpp4 缺失菌株均无病原性,而 kpp2 缺失突变体仅在发病机理中减毒。在这里,我们表明表达不可磷酸化等位基因 kpp2 T182A / Y184F 的菌株在肿瘤诱导中受到严重影响,并在早期感染相关的分化中表现出缺陷。

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