4.7 Article

Susceptibility factor StEXA1 interacts with StnCBP to facilitate potato virus Y accumulation through the stress granule-dependent RNA regulatory pathway in potato

Journal

HORTICULTURE RESEARCH
Volume 9, Issue -, Pages -

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/hr/uhac159

Keywords

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Funding

  1. National Natural Science Foundation of China [31971989]
  2. China Agriculture Research System of MOF and MARA [CARS09-P07]

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Plant viruses depend on multiple host factors for translation, replication, and movement during infection. The EXA1 gene has been identified as a susceptibility gene for potexvirus, lolavirus, and bacterial and oomycete pathogens. Knockdown of StEXA1 in potato confers resistance to potato virus Y (PVY) in a strain-specific manner. StEXA1 interacts with PVY's HC-Pro protein through a member of eIF4Es and facilitates PVY accumulation through the stress granule-dependent RNA regulatory pathway.
Plant viruses recruit multiple host factors for translation, replication, and movement in the infection process. The loss-of-function mutation of the susceptibility genes will lead to the loss of susceptibility to viruses, which is referred to as 'recessive resistance'. Essential for potexvirus Accumulation 1 (EXA1) has been identified as a susceptibility gene required for potexvirus, lolavirus, and bacterial and oomycete pathogens. In this study, EXA1 knockdown in potato (StEXA1) was found to confer novel resistance to potato virus Y (PVY, potyvirus) in a strain-specific manner. It significantly compromised PVYO accumulation but not PVYN:O and PVYNTN. Further analysis revealed that StEXA1 is associated with the HC-Pro of PVY through a member of eIF4Es (StnCBP). HC-Pro(O) and HC-Pro(N), two HC-Pro proteins from PVYO and PVYN, exhibited strong and weak interactions with StnCBP, respectively, due to their different spatial conformation. Moreover, the accumulation of PVYO was mainly dependent on the stress granules (SGs) induced by StEXA1 and StnCBP, whereas PVYN:O and PVYNTN could induce SGs by HC-Pro(N) independently through an unknown mechanism. These results could explain why StEXA1 or StnCBP knockdown conferred resistance to PVYO but not to PVYN:O and PVYNTN. In summary, our results for the first time demonstrate that EXA1 can act as a susceptibility gene for PVY infection. Finally, a hypothetical model was proposed for understanding the mechanism by which StEXA1 interacts with StnCBP to facilitate PVY accumulation in potato through the SG-dependent RNA regulatory pathway.

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