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Extracellular Matrix Protein Gene, EMP1, Is Required for Appressorium Formation and Pathogenicity of the Rice Blast Fungus, Magnaporthe grisea

机译:稻瘟病菌稻瘟病菌的附着层形成和致病性需要细胞外基质蛋白基因EMP1

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Magnaporthe grisea, the causal fungus of rice blast, forms a specialized infection structure called an appressorium that is crucial for host plant penetration. A cDNA clone of M. grisea, showing strong sequence homology to FEM1 of Fusarium oxysporum and encoding an extracellular matrix protein, was isolated during an expressed sequence tag (EST) analysis of an appressorium cDNA library and named extracellular matrix protein 1 (EMP1). Sequence analysis of the corresponding genomic clone revealed that EMP1 contains an open reading frame of 685 nucleotides encoding 207 amino acids. The estimated molecular weight of the protein product was 20.5 kDa with a pI of 7.84. It contains an 18 amino acid N-terminal secretion signal sequence, as well as four potential N-glycosylation sites. At its C-terminus, the protein contains a 16 amino acid sequence with the characteristics of a glycosylphosphatidylinositol (GPI) anchor addition signal. Northern blot analysis showed that EMP1 transcripts accumulate during appressorium formation but not during vegetative growth. An EMP1 null mutant, emp1, generated by targeted gene disruption, exhibited reduced levels of appressorium formation and pathogenicity but no effect on mycelial growth rate or conidiation ability. These data suggest that EMP1 plays important roles in appressorium formation and the pathogenicity of M. grisea.
机译:稻瘟病的病原真菌稻瘟病菌(Magnaporthe grisea)形成了一种专门的感染结构,称为an虫,对宿主植物的渗透至关重要。显示了与尖孢镰刀菌FEM1的序列同源性很强并编码细胞外基质蛋白的稻瘟病菌的cDNA克隆,该过程在附子cDNA文库的表达序列标签(EST)分析中被分离出来,并命名为细胞外基质蛋白1(EMP1)。相应基因组克隆的序列分析表明,EMP1包含一个685个核苷酸的开放阅读框,编码207个氨基酸。蛋白质产物的估计分子量为20.5 kDa,pI为7.84。它包含一个18个氨基酸的N端分泌信号序列,以及四个潜在的N-糖基化位点。在其C端,该蛋白质包含16个氨基酸序列,具有糖基磷脂酰肌醇(GPI)锚定添加信号的特征。 Northern印迹分析表明,EMP1转录本在app形成期间积累,但在营养生长期间不积累。 EMP1空突变体emp1,由有针对性的基因破坏产生,表现出降低的ress形成和致病性,但对菌丝生长速率或分生能力没有影响。这些数据表明,EMP1在病原菌的形成和稻瘟病菌的致病性中起重要作用。

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