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

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 Accu...

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Detalles Bibliográficos
Autores principales: Chen, Ruhao, Tu, Zhen, He, Changzheng, Nie, Xianzhou, Li, Kun, Fei, Sitian, Song, Botao, Nie, Bihua, Xie, Conghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9531334/
https://www.ncbi.nlm.nih.gov/pubmed/36204208
http://dx.doi.org/10.1093/hr/uhac159
Descripción
Sumario: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 PVY(O) accumulation but not PVY(N:O) and PVY(NTN). 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 PVY(O) and PVY(N), exhibited strong and weak interactions with StnCBP, respectively, due to their different spatial conformation. Moreover, the accumulation of PVY(O) was mainly dependent on the stress granules (SGs) induced by StEXA1 and StnCBP, whereas PVY(N:O) and PVY(NTN) could induce SGs by HC-Pro(N) independently through an unknown mechanism. These results could explain why StEXA1 or StnCBP knockdown conferred resistance to PVY(O) but not to PVY(N:O) and PVY(NTN). 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.