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Distinct roles of the YPEL gene family in development and pathogenicity in the ascomycete fungus Magnaporthe oryzae.

Members of the Yippee-like (YPEL) gene family are highly conserved in eukaryotes and are homologous to the Drosophila yippee gene. In this study, we functionally characterized two YPEL-homologous genes, MoYPEL1 and MoYPEL2, in the rice blast pathogen Magnaporthe oryzae using the deletion mutants ΔMoypel1ΔMoypel2, and ΔΔMoypel1,2. The MoYPEL1 deletion mutant was significantly defective in conidiation and unable to undergo appressorium development;

Han JHShin JHLee YHKim KS.

Sci Rep. 2018 Sep 27;8(1):14461. doi: 10.1038/s41598-018-32633-6.

Abstract

Members of the Yippee-like (YPEL) gene family are highly conserved in eukaryotes and are homologous to the Drosophila yippee gene. In this study, we functionally characterized two YPEL-homologous genes, MoYPEL1 and MoYPEL2, in the rice blast pathogen Magnaporthe oryzae using the deletion mutants ΔMoypel1ΔMoypel2, and ΔΔMoypel1,2. The MoYPEL1 deletion mutant was significantly defective in conidiation and unable to undergo appressorium development; however, deletion of MoYPEL2 resulted in a significant increase in conidiation and the abnormal development of two appressoria per conidium. These data demonstrate the opposite roles of each member of the YPEL gene family during the development of Moryzae. The double mutant was phenotypically similar to the ΔMoypel1 mutant in conidiation, but similar to the ΔMoypel2 mutant in appressorium development. Subcellular localization of the MoYPEL1 protein was dynamic during appressorium development, while the MoYPEL2 protein consistently localized within the nuclei during developmental stages. Our studies indicate that the two YPEL gene family members play distinct roles in the developmental stages of Moryzae, furthering our understanding of disease dissemination and development in fungi.

 

See https://www.ncbi.nlm.nih.gov/pubmed/30262874

 

Figure 3: Subcellular localization of MoYPEL protein in Moryzae. (A) A dynamic change in MoYPEL1:sGFP localization. Briefly, the MoYPEL1:sGFP fusion protein was initially localized in conidium cytoplasm, followed by aggregation next to nuclei and diffuse distribution in the cytoplasm. Newly aggregated MoYPEL1:sGFP protein emerged at both sides of the nucleus during germ tube development. An aggregated form of MoYPEL1:sGFP protein subsequently appeared in the appressorium initial, and disappeared following nuclear division during appressorium development. Conidia were observed on coverslips at the indicated time points during appressorium development. (B) Localization of MoYPEL2:sGFP. The obvious colocalization (orange) of MoYPEL2:sGFP and histone HI:RFP fusion proteins was observed during appressorium development and hyphal growth. Scale bars = 20 µm.

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