MoSec61β, the beta subunit of Sec61, is involved in fungal development and pathogenicity, plant immunity, and ER-phagy in Magnaporthe oryzae

References

• Couch BC, Kohn LM. A multilocus gene genealogy concordant with host preference indicates segregation of a new species, Magnaporthe oryzae, from M. grisea. Mycologia. 2002;94:683–693. PMID:21156541.
   PubMed Web of Science ®Google Scholar
• Dean RA. Signal pathways and appressorium morphogenesis. Annu Rev Phytopathol. 1997;35:211–234. PMID:15012522.
   PubMed Web of Science ®Google Scholar
• Thines E, Weber RW, Talbot NJ. MAP kinase and protein kinase A-dependent mobilization of triacylglycerol and glycogen during appressorium turgor generation by Magnaporthe grisea. Plant Cell. 2000;12:1703–1718. PMID:11006342.
   PubMed Web of Science ®Google Scholar
• Peng Y, van Wersch R, Zhang Y. Convergent and divergent signaling in PAMP-triggered immunity and effector-triggered immunity. Mol Plant Microbe Interact. 2018;31:403–409. PMID:29135338.
   PubMed Web of Science ®Google Scholar
• Medzhitov R, Janeway CJ. Innate immunity: the virtues of a nonclonal system of recognition. CELL. 1997;91:295–298. PMID:9363937.
   PubMed Web of Science ®Google Scholar
• Zhou Z, Pang Z, Li G, et al. Endoplasmic reticulum membrane-bound MoSec62 is involved in the suppression of rice immunity and is essential for the pathogenicity of Magnaporthe oryzae. Mol Plant Pathol. 2016;17:1211–1222. PMID:26679839.
   PubMed Web of Science ®Google Scholar
• Wang C, Liu Y, Liu L, et al. The biotrophy-associated secreted protein 4 (BAS4) participates in the transition of Magnaporthe oryzae from the biotrophic to the necrotrophic phase. Saudi J Biol Sci. 2019;26:795–807. PMID:31049006.
   PubMed Web of Science ®Google Scholar
• Kankanala P, Czymmek K, Valent B. Roles for rice membrane dynamics and plasmodesmata during biotrophic invasion by the blast fungus. Plant Cell. 2007;19:706–724. PMID:17322409.
   PubMed Web of Science ®Google Scholar
• Khang CH, Berruyer R, Giraldo MC, et al. Translocation of Magnaporthe oryzae effectors into rice cells and their subsequent cell-to-cell movement. Plant Cell. 2010;22:1388–1403. PMID:20435900.
   PubMed Web of Science ®Google Scholar
• Giraldo MC, Dagdas YF, Gupta YK, et al. Two distinct secretion systems facilitate tissue invasion by the rice blast fungus Magnaporthe oryzae. Nat Commun. 2013;4:1996. PMID:23774898.
   PubMed Web of Science ®Google Scholar
• Wang Y, Wang Y. Trick or treat: microbial pathogens evolved apoplastic effectors modulating plant susceptibility to infection. Mol Plant Microbe Interact. 2018;31:6–12. PMID:29090656.
   PubMed Web of Science ®Google Scholar
• Mentlak TA, Kombrink A, Shinya T, et al. Effector-mediated suppression of chitin-triggered immunity by magnaporthe oryzae is necessary for rice blast disease. Plant Cell. 2012;24:322–335. PMID:22267486.
   PubMed Web of Science ®Google Scholar
• Viotti C. ER to golgi-dependent protein secretion: the conventional pathway. Methods Mol Biol. 2016;1459:3–29. PMID:27665548.
   PubMedGoogle Scholar
• Nie H, Zhang L, Zhuang H, et al. Secreted protein MoHrip2 is required for full virulence of Magnaporthe oryzae and modulation of rice immunity. Appl Microbiol Biotechnol. 2019;103:6153–6167. PMID:31154490.
   PubMed Web of Science ®Google Scholar
• Zhang S, Xu JR. Effectors and effector delivery in Magnaporthe oryzae. PLOS Pathog. 2014;10:e1003826. PMID:24391496.
   PubMed Web of Science ®Google Scholar
• Polgar N, Lee AJ, Lui VH, et al. The exocyst gene Sec10 regulates renal epithelial monolayer homeostasis and apoptotic sensitivity. Am J Physiol Cell Physiol. 2015;309:C190–201. PMID:26040895.
   PubMed Web of Science ®Google Scholar
• Bebok Z, Mazzochi C, King SA, et al. The mechanism underlying cystic fibrosis transmembrane conductance regulator transport from the endoplasmic reticulum to the proteasome includes Sec61beta and a cytosolic, deglycosylated intermediary. J Biol Chem. 1998;273:29873–29878. PMID:9792704.
   PubMed Web of Science ®Google Scholar
• Mothes W, Prehn S, Rapoport TA. Systematic probing of the environment of a translocating secretory protein during translocation through the ER membrane. Embo J. 1994;13:3973–3982. PMID:8076593.
   PubMed Web of Science ®Google Scholar
• Esnault Y, Blondel MO, Deshaies RJ, et al. The yeast SSS1 gene is essential for secretory protein translocation and encodes a conserved protein of the endoplasmic reticulum. Embo J. 1993;12:4083–4093. PMID:8223425.
   PubMed Web of Science ®Google Scholar
• Feng D, Zhao X, Soromani C, et al. The transmembrane domain is sufficient for Sbh1p function, its association with the Sec61 complex, and interaction with Rtn1p. Journal of Biological Chemistry. 2007;282(42):30618–30628. PMID:17699516.
   PubMed Web of Science ®Google Scholar
• Kelkar A, Dobberstein B. Sec61beta, a subunit of the Sec61 protein translocation channel at the endoplasmic reticulum, is involved in the transport of Gurken to the plasma membrane. Bmc Cell Biol. 2009;10:11. PMID:19226464.
   PubMedGoogle Scholar
• Zhang WJ, Hanisch S, Kwaaitaal M, et al. A component of the Sec61 ER protein transporting pore is required for plant susceptibility to powdery mildew. Front Plant Sci. 2013;4:127. PMID:23720664.
   PubMed Web of Science ®Google Scholar
• Wang ZY, Soanes DM, Kershaw MJ, et al. Functional analysis of lipid metabolism in Magnaporthe grisea reveals a requirement for peroxisomal fatty acid beta-oxidation during appressorium-mediated plant infection. Mol Plant Microbe Interact. 2007;20:475–491. PMID:17506326.
   PubMed Web of Science ®Google Scholar
• Li R, Jia Z, Trush MA. Defining ROS in biology and medicine. React Oxyg Species (Apex). 2016;1:9–21. PMID:29707643.
   PubMedGoogle Scholar
• Nakashita H, Yoshioka K, Takayama M, et al. Characterization of PBZ1, a probenazole-inducible gene, in suspension-cultured rice cells. Biosci Biotechnol Biochem. 2001;65:205–208. PMID:11272832.
   PubMed Web of Science ®Google Scholar
• Wang C, Li C, Duan G, et al. Overexpression of Magnaporthe oryzae systemic defense trigger 1 (MoSDT1) confers improved rice blast resistance in rice. Int J Mol Sci. 2019;20. PMID:31557947. DOI:https://doi.org/10.3390/ijms20194762.
   Google Scholar
• Luna E, Pastor V, Robert J, et al. Callose deposition: a multifaceted plant defense response. Mol Plant Microbe Interact. 2011;24:183–193. PMID:20955078.
   PubMed Web of Science ®Google Scholar
• Lang S, Pfeffer S, Lee PH, et al. An update on Sec61 channel functions, mechanisms, and related diseases. Front Physiol. 2017;8:887. PMID:29163222.
   PubMed Web of Science ®Google Scholar
• Chino H, Mizushima N. ER-Phagy: quality control and turnover of endoplasmic reticulum. Trends Cell Biol. 2020;30:384–398. PMID:32302550.
   PubMed Web of Science ®Google Scholar
• Hwang J, Qi L. Quality control in the endoplasmic reticulum: crosstalk between ERAD and UPR pathways. Trends Biochem Sci. 2018;43:593–605. PMID:30056836.
   PubMed Web of Science ®Google Scholar
• Tang W, Jiang H, Aron O, et al. Endoplasmic reticulum-associated degradation mediated by MoHrd1 and MoDer1 is pivotal for appressorium development and pathogenicity of Magnaporthe oryzae. Environ Microbiol. 2020. PMID:32410295. DOI:https://doi.org/10.1111/1462-2920.15069.
   Google Scholar
• Chen XL, Liu C, Tang B, et al. Quantitative proteomics analysis reveals important roles of N-glycosylation on ER quality control system for development and pathogenesis in Magnaporthe oryzae. Plos Pathog. 2020;16:e1008355. PMID:32092131.
   PubMed Web of Science ®Google Scholar
• Yi M, Chi MH, Khang CH, et al. The ER chaperone LHS1 is involved in asexual development and rice infection by the blast fungus Magnaporthe oryzae. Plant Cell. 2009;21:681–695. PMID:19252083.
   PubMed Web of Science ®Google Scholar
• Toikkanen JH, Miller KJ, Soderlund H, et al. The beta subunit of the Sec61p endoplasmic reticulum translocon interacts with the exocyst complex in Saccharomyces cerevisiae. J Biol Chem. 2003;278:20946–20953. PMID:12665530.
   PubMed Web of Science ®Google Scholar
• Liu XH, Lu JP, Zhang L, et al. Involvement of a Magnaporthe grisea serine/threonine kinase gene, MgATG1, in appressorium turgor and pathogenesis. Eukaryot Cell. 2007;6:997–1005. PMID:17416896.
   PubMedGoogle Scholar
• Romisch K. Endoplasmic reticulum-associated degradation. Annu Rev Cell Dev Biol. 2005;21:435–456. PMID:16212502.
   PubMed Web of Science ®Google Scholar
• Bernales S, Schuck S, Walter P. ER-phagy: selective autophagy of the endoplasmic reticulum. Autophagy. 2007;3:285–287. PMID:17351330.
   PubMed Web of Science ®Google Scholar
• Talbot NJ, Ebbole DJ, Hamer JE. Identification and characterization of MPG1, a gene involved in pathogenicity from the rice blast fungus Magnaporthe grisea. Plant Cell. 1993;5:1575–1590. PMID:8312740.
   PubMed Web of Science ®Google Scholar
• Cao H, Huang P, Zhang L, et al. Characterization of 47 Cys2 -His2 zinc finger proteins required for the development and pathogenicity of the rice blast fungus Magnaporthe oryzae. New Phytol. 2016;211:1035–1051. PMID:27041000.
   PubMed Web of Science ®Google Scholar
• Kim S, Ahn IP, Rho HS, et al. MHP1, a Magnaporthe grisea hydrophobin gene, is required for fungal development and plant colonization. Mol Microbiol. 2005;57:1224–1237. PMID:16101997.
   PubMed Web of Science ®Google Scholar
• Howard RJ, Ferrari MA, Roach DH, et al. Penetration of hard substrates by a fungus employing enormous turgor pressures. Proc Natl Acad Sci USA. 1991;88:11281–11284. PMID:1837147.
   PubMed Web of Science ®Google Scholar