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The small GTPase MoYpt7 is required for membrane fusion in autophagy and pathogenicity of Magnaporthe oryzae

Summary Rab GTPases are required for vesicle–vacuolar fusion during vacuolar biogenesis in fungi. To date, little is known about the biological functions of the Rab small GTPase components in Magnaporthe oryzae. In this study, we investigated MoYpt7 of M. oryzae, a homologue of the small Ras‐like GT...

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Published in:Environmental microbiology 2015-11, Vol.17 (11), p.4495-4510
Main Authors: Liu, Xiao-Hong, Chen, Si-Miao, Gao, Hui-Min, Ning, Guo-Ao, Shi, Huan-Bin, Wang, Yao, Dong, Bo, Qi, Yao-Yao, Zhang, Dong-Mei, Lu, Guo-Dong, Wang, Zong-Hua, Zhou, Jie, Lin, Fu-Cheng
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container_issue 11
container_start_page 4495
container_title Environmental microbiology
container_volume 17
creator Liu, Xiao-Hong
Chen, Si-Miao
Gao, Hui-Min
Ning, Guo-Ao
Shi, Huan-Bin
Wang, Yao
Dong, Bo
Qi, Yao-Yao
Zhang, Dong-Mei
Lu, Guo-Dong
Wang, Zong-Hua
Zhou, Jie
Lin, Fu-Cheng
description Summary Rab GTPases are required for vesicle–vacuolar fusion during vacuolar biogenesis in fungi. To date, little is known about the biological functions of the Rab small GTPase components in Magnaporthe oryzae. In this study, we investigated MoYpt7 of M. oryzae, a homologue of the small Ras‐like GTPase Ypt7 in Saccharomyces cerevisiae. Cellular localization assays showed that MoYpt7 was predominantly localized to vacuolar membranes. Using a targeted gene disruption strategy, a ΔMoYPT7 mutant was generated that exhibited defects in mycelial growth and production of conidia. The conidia of the ΔMoYPT7 mutant were malformed and defective in the formation of appressoria. Consequently, the ΔMoYPT7 mutant failed to cause disease in rice and barley. Furthermore, the ΔMoYPT7 mutant showed impairment in autophagy, breached cell wall integrity, and higher sensitivity to both calcium and heavy metal stress. Transformants constitutively expressing an active MoYPT7 allele (MoYPT7‐CA, Gln67Leu) exhibited distinct phenotypes from the ΔMoYPT7 mutant. Expression of MoYPT7‐CA in MoYpt7 reduced pathogenicity and produced more appressoria‐forming single‐septum conidia. These results indicate that MoYPT7 is required for fungal morphogenesis, vacuole fusion, autophagy, stress resistance and pathogenicity in M. oryzae.
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To date, little is known about the biological functions of the Rab small GTPase components in Magnaporthe oryzae. In this study, we investigated MoYpt7 of M. oryzae, a homologue of the small Ras‐like GTPase Ypt7 in Saccharomyces cerevisiae. Cellular localization assays showed that MoYpt7 was predominantly localized to vacuolar membranes. Using a targeted gene disruption strategy, a ΔMoYPT7 mutant was generated that exhibited defects in mycelial growth and production of conidia. The conidia of the ΔMoYPT7 mutant were malformed and defective in the formation of appressoria. Consequently, the ΔMoYPT7 mutant failed to cause disease in rice and barley. Furthermore, the ΔMoYPT7 mutant showed impairment in autophagy, breached cell wall integrity, and higher sensitivity to both calcium and heavy metal stress. Transformants constitutively expressing an active MoYPT7 allele (MoYPT7‐CA, Gln67Leu) exhibited distinct phenotypes from the ΔMoYPT7 mutant. Expression of MoYPT7‐CA in MoYpt7 reduced pathogenicity and produced more appressoria‐forming single‐septum conidia. These results indicate that MoYPT7 is required for fungal morphogenesis, vacuole fusion, autophagy, stress resistance and pathogenicity in M. oryzae.</description><identifier>ISSN: 1462-2912</identifier><identifier>EISSN: 1462-2920</identifier><identifier>DOI: 10.1111/1462-2920.12903</identifier><identifier>PMID: 25991510</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Amino Acid Sequence ; Autophagy ; Autophagy - genetics ; Calcium - pharmacology ; Cell Wall - metabolism ; Fungal Proteins - genetics ; Fungal Proteins - metabolism ; Hordeum - microbiology ; Hordeum vulgare ; Magnaporthe - genetics ; Magnaporthe - pathogenicity ; Membrane Fusion - genetics ; Membrane Fusion - physiology ; Metals, Heavy - pharmacology ; Molecular Sequence Data ; Oryza - microbiology ; Phenotype ; Plant Diseases - microbiology ; rab GTP-Binding Proteins - genetics ; rab GTP-Binding Proteins - metabolism ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - genetics ; Spores, Fungal - genetics ; Spores, Fungal - metabolism ; Stress, Physiological - genetics ; Vacuoles - metabolism ; Virulence - genetics</subject><ispartof>Environmental microbiology, 2015-11, Vol.17 (11), p.4495-4510</ispartof><rights>2015 Society for Applied Microbiology and John Wiley &amp; Sons Ltd</rights><rights>2015 Society for Applied Microbiology and John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2015 Society for Applied Microbiology and John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25991510$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Xiao-Hong</creatorcontrib><creatorcontrib>Chen, Si-Miao</creatorcontrib><creatorcontrib>Gao, Hui-Min</creatorcontrib><creatorcontrib>Ning, Guo-Ao</creatorcontrib><creatorcontrib>Shi, Huan-Bin</creatorcontrib><creatorcontrib>Wang, Yao</creatorcontrib><creatorcontrib>Dong, Bo</creatorcontrib><creatorcontrib>Qi, Yao-Yao</creatorcontrib><creatorcontrib>Zhang, Dong-Mei</creatorcontrib><creatorcontrib>Lu, Guo-Dong</creatorcontrib><creatorcontrib>Wang, Zong-Hua</creatorcontrib><creatorcontrib>Zhou, Jie</creatorcontrib><creatorcontrib>Lin, Fu-Cheng</creatorcontrib><title>The small GTPase MoYpt7 is required for membrane fusion in autophagy and pathogenicity of Magnaporthe oryzae</title><title>Environmental microbiology</title><addtitle>Environ Microbiol</addtitle><description>Summary Rab GTPases are required for vesicle–vacuolar fusion during vacuolar biogenesis in fungi. To date, little is known about the biological functions of the Rab small GTPase components in Magnaporthe oryzae. In this study, we investigated MoYpt7 of M. oryzae, a homologue of the small Ras‐like GTPase Ypt7 in Saccharomyces cerevisiae. Cellular localization assays showed that MoYpt7 was predominantly localized to vacuolar membranes. Using a targeted gene disruption strategy, a ΔMoYPT7 mutant was generated that exhibited defects in mycelial growth and production of conidia. The conidia of the ΔMoYPT7 mutant were malformed and defective in the formation of appressoria. Consequently, the ΔMoYPT7 mutant failed to cause disease in rice and barley. Furthermore, the ΔMoYPT7 mutant showed impairment in autophagy, breached cell wall integrity, and higher sensitivity to both calcium and heavy metal stress. Transformants constitutively expressing an active MoYPT7 allele (MoYPT7‐CA, Gln67Leu) exhibited distinct phenotypes from the ΔMoYPT7 mutant. Expression of MoYPT7‐CA in MoYpt7 reduced pathogenicity and produced more appressoria‐forming single‐septum conidia. 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To date, little is known about the biological functions of the Rab small GTPase components in Magnaporthe oryzae. In this study, we investigated MoYpt7 of M. oryzae, a homologue of the small Ras‐like GTPase Ypt7 in Saccharomyces cerevisiae. Cellular localization assays showed that MoYpt7 was predominantly localized to vacuolar membranes. Using a targeted gene disruption strategy, a ΔMoYPT7 mutant was generated that exhibited defects in mycelial growth and production of conidia. The conidia of the ΔMoYPT7 mutant were malformed and defective in the formation of appressoria. Consequently, the ΔMoYPT7 mutant failed to cause disease in rice and barley. Furthermore, the ΔMoYPT7 mutant showed impairment in autophagy, breached cell wall integrity, and higher sensitivity to both calcium and heavy metal stress. Transformants constitutively expressing an active MoYPT7 allele (MoYPT7‐CA, Gln67Leu) exhibited distinct phenotypes from the ΔMoYPT7 mutant. Expression of MoYPT7‐CA in MoYpt7 reduced pathogenicity and produced more appressoria‐forming single‐septum conidia. These results indicate that MoYPT7 is required for fungal morphogenesis, vacuole fusion, autophagy, stress resistance and pathogenicity in M. oryzae.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>25991510</pmid><doi>10.1111/1462-2920.12903</doi><tpages>16</tpages></addata></record>
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subjects Amino Acid Sequence
Autophagy
Autophagy - genetics
Calcium - pharmacology
Cell Wall - metabolism
Fungal Proteins - genetics
Fungal Proteins - metabolism
Hordeum - microbiology
Hordeum vulgare
Magnaporthe - genetics
Magnaporthe - pathogenicity
Membrane Fusion - genetics
Membrane Fusion - physiology
Metals, Heavy - pharmacology
Molecular Sequence Data
Oryza - microbiology
Phenotype
Plant Diseases - microbiology
rab GTP-Binding Proteins - genetics
rab GTP-Binding Proteins - metabolism
Saccharomyces cerevisiae
Saccharomyces cerevisiae - genetics
Spores, Fungal - genetics
Spores, Fungal - metabolism
Stress, Physiological - genetics
Vacuoles - metabolism
Virulence - genetics
title The small GTPase MoYpt7 is required for membrane fusion in autophagy and pathogenicity of Magnaporthe oryzae
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