A positive‐charged patch and stabilized hydrophobic core are essential for avirulence function of AvrPib in the rice blast fungus

  • Xin Zhang
    Ministry of Agriculture Key Laboratory of Pest Monitoring and Green Management College of Plant Protection China Agricultural University Beijing 100193 China
  • Dan He
    Ministry of Agriculture Key Laboratory of Pest Monitoring and Green Management College of Plant Protection China Agricultural University Beijing 100193 China
  • Yanxiang Zhao
    Ministry of Agriculture Key Laboratory of Pest Monitoring and Green Management College of Plant Protection China Agricultural University Beijing 100193 China
  • Xilan Cheng
    Ministry of Agriculture Key Laboratory of Pest Monitoring and Green Management College of Plant Protection China Agricultural University Beijing 100193 China
  • Wensheng Zhao
    Ministry of Agriculture Key Laboratory of Pest Monitoring and Green Management College of Plant Protection China Agricultural University Beijing 100193 China
  • Ian A. Taylor
    Macromolecular Structure Laboratory The Francis Crick Institute 1 Midland Road London NW1 1AT UK
  • Jun Yang
    Ministry of Agriculture Key Laboratory of Pest Monitoring and Green Management College of Plant Protection China Agricultural University Beijing 100193 China
  • Junfeng Liu
    Ministry of Agriculture Key Laboratory of Pest Monitoring and Green Management College of Plant Protection China Agricultural University Beijing 100193 China
  • You‐Liang Peng
    Ministry of Agriculture Key Laboratory of Pest Monitoring and Green Management College of Plant Protection China Agricultural University Beijing 100193 China

説明

<jats:title>Summary</jats:title><jats:p>Fungal avirulence effectors, a key weapon utilized by pathogens to promote their infection, are recognized by immune receptors to boost host R gene‐mediated resistance. Many avirulence effectors share sparse sequence homology to proteins with known functions, and their molecular and biochemical functions together with the evolutionary relationship among different members remain largely unknown. Here, the crystal structure of AvrPib, an avirulence effector from <jats:italic>Magnaporthe oryzae</jats:italic>, was determined and showed a high degree of similarity to the <jats:styled-content><jats:italic>M</jats:italic></jats:styled-content>. <jats:italic>oryzae</jats:italic> <jats:styled-content>A</jats:styled-content>vrs and To<jats:styled-content>x</jats:styled-content>B (<jats:styled-content style="fixed-case">MAX</jats:styled-content>) effectors. Compared with other <jats:styled-content style="fixed-case">MAX</jats:styled-content> effectors, AvrPib has a distinct positive‐charge patch formed by five positive‐charged residues (K29, K30, R50, K52 and K70) on the surface. These five key residues were essential to avirulence function of AvrPib and affected its nuclear localization into host cells. Moreover, residues V39 and V58, which locate in the hydrophobic core of the structure, cause loss of function of AvrPib by single‐point mutation in natural isolates. In comparison with the wild‐type AvrPib, the V39A or V58A mutations resulted in a partial or entire loss of secondary structure elements. Taken together, our results suggest that differences in the surface charge distribution of avirulence proteins could be one of the major bases for the variation in effector–receptor specificity, and that destabilization of the hydrophobic core is one of the major mechanisms employed by AvrPib for the fungus to evade recognition by resistance factors in the host cell.</jats:p>

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