Function of PoLAE2, a laeA homolog, in appressorium formation and cAMP signal transduction in Pyricularia oryzae

References

• Talbot NJ. On the trail of cereal killer: exploring the biology of Magnaporthe grisea. Annu Rev of Microbiol. 2003;57:177–202.
   PubMed Web of Science ®Google Scholar
• Ryder LS, Talbot NJ. Regulation of appressorium development in pathogenic fungi. Curr Opin Plant Biol. 2015;26:8–13.
   PubMed Web of Science ®Google Scholar
• Wilson RA, Talbot NJ. Under pressure; investigating the biology of plant infection by Magnaporthe oryzae. Microbiology. 2009;7:158–195.
   Web of Science ®Google Scholar
• Li G, Zhou X, Xu JR. The genetic control of infection-related development in Magnaporthe oryzae. Curr Opin Microbiol. 2012;15:678–684.
   PubMed Web of Science ®Google Scholar
• Palmer JM, Keller NP. Secondary metabolism in fungi: does chromosomal location matter? Curr Opin Microbiol. 2010;13:431–436.
   PubMed Web of Science ®Google Scholar
• Ö B, Krappmann S, Ni M, et al. VelB/VeA/LaeA complex coordinates light signal with fungal development and secondary metabolism. Science. 2008;320:1504–1506.
   PubMed Web of Science ®Google Scholar
• Chang PK, Scharfenstein LL, Ehrlich KC, et al. Effects of laeA deletion on Aspergillus flavus conidial development and hydrophobicity may contribute to loss of aflatoxin production. Fungal Biol. 2011;116:98–307.
   PubMed Web of Science ®Google Scholar
• Bok JW, Nancy PK. LaeA, a regulator of secondary metabolism in Aspergillus spp. Eukaryot Cell. 2004;3:527–535.
   PubMed Web of Science ®Google Scholar
• Jain S, Nancy PK. Insights to fungal biology through LaeA sleuthing. Fungal Biol Rev. 2013;27:51–59.
   Web of Science ®Google Scholar
• Saha P, Ghosh S, Roy-Barman S. MoLAEA regulates secondary metabolism in Magnaporthe oryzae. mSphere. 2020;5:1–22.
   Web of Science ®Google Scholar
• Abe A, Elegado EB, Sone T. Construction of pDESTR, a GATEWAY vector for gene disruption in filamentous fungi. Curr Microbiol. 2006;52:210–215.
   PubMed Web of Science ®Google Scholar
• Miki S, Matsui K, Kito H, et al. Molecular cloning and characterization of the AVR-Pia locus from a Japanese field isolate of Magnaporthe oryzae. Mol Plant Pathol. 2009;10:361–374.
   PubMed Web of Science ®Google Scholar
• Sone T, Abe T, Yoshida N, et al. DNA fingerprint and electrophoretic karyotyping of Japanese isolates of rice blast fungus. Ann Phytopathol Soc Jpn. 1997;63:155–163.
   Google Scholar
• Sornkom W, Asano K, Sone T. Use of native promoter-eGFP as a gene reporter on onion epidermis to analyze gene expression of AVR-Pia, an avirulence of rice blast pathogen. Engineer J. 2015;19:86–93.
   Google Scholar
• Sornkom W, Miki S, Takeuchi S, et al. Fluorescent reporter analysis revealed the timing and localization of AVR-Pia expression, an avirulence effector of Magnaporthe oryzae. Mol Plant Pathol. 2017;18:1138–1149.
   PubMed Web of Science ®Google Scholar
• Koga H, Dohi K, Nakayachi O, et al. A novel inoculation method of Magnaporthe grisea for cytological observation of the infection process using intact leaf sheaths of rice plants. Physiol Mol Plant Pathol. 2004;64:67–72.
   Web of Science ®Google Scholar
• Lee YH, Dean RA. cAMP regulates infection structure formation in the plant pathogenic fungus Magnaporthe grisea. Plant Cell. 1993;5:693–700.
   PubMed Web of Science ®Google Scholar
• Skamnioti P, Gurr SJ. Magnaporthe grisea cutinase 2 mediates appressorium differentiation and host penetration and is required for full virulence. Plant Cell. 2007;19:2674–2689.
   PubMed Web of Science ®Google Scholar
• Liu H, Suresh A, Willard FS, et al. Rgs1 regulates multiple Gα subunits in Magnaporthe pathogenesis, asexual growth and thigmotropism. Embo J. 2007;16:690–700.
   Google Scholar
• Spoto G, Whitehead E, Ferraro A, et al. A reverse-phase HPLC method for cAMP phosphodiesterase activity. Anal Biochem. 1991;196:207–210.
   PubMed Web of Science ®Google Scholar
• Choi W, Dean RA. The adenylate cyclase gene MAC1 of Magnaporthe grisea controls appressorium formation and other aspects of growth and development. Plant Cell. 1997;9:1973–1983.
   PubMed Web of Science ®Google Scholar
• Ramanujam R, Naqvi NI. PdeH, a high-affinity cAMP phosphodiesterase, is a key regulator of asexual and pathogenic differentiation in Magnaporthe oryzae. PLoS Pathog. 2010;6:1–23.
   Web of Science ®Google Scholar
• Yangyong L, Ang L, Zhai H, et al. Insight into the global regulation of laeA in Aspergillus flavus base on proteomic profiling. Int J Food Microbiol. 2018;284:11–21.
   PubMed Web of Science ®Google Scholar
• Izawa M, Takekawa O, Arie T, et al. Inhibition of histone deacetylase causes reduction of appressorium formation in rice blast fungus Magnaporthe oryzae. J Gen Appl Microbiol. 2009;55:489–498.
   PubMed Web of Science ®Google Scholar
• Lee J, Lee JJ, Jeon J. A histone deacetylase, MoHOS2 regulates asexual development and virulence in the rice blast fungus. J Microbiol. 2019;57:1115–1125.
   PubMed Web of Science ®Google Scholar