Autophagy-associated alpha-arrestin signaling is required for conidiogenous cell development in Magnaporthe oryzae

Conidiation patterning is evolutionarily complex and mechanism concerning conidiogenous cell differentiation remains largely unknown. Magnaporthe oryzae conidiates in a sympodial way and uses its conidia to infect host and disseminate blast disease. Arrestins are multifunctional proteins that modula...

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Main Authors: Dong, Bo, Xu, Xiaojin, Chen, Guoqing, Zhang, Dandan, Tang, Mingzhi, Xu, Fei, Liu, Xiaohong, Wang, Hua, Zhou, Bo
Format: Journal Article
Language:Inglés
Published: Springer 2016
Online Access:https://hdl.handle.net/10568/165223
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author Dong, Bo
Xu, Xiaojin
Chen, Guoqing
Zhang, Dandan
Tang, Mingzhi
Xu, Fei
Liu, Xiaohong
Wang, Hua
Zhou, Bo
author_browse Chen, Guoqing
Dong, Bo
Liu, Xiaohong
Tang, Mingzhi
Wang, Hua
Xu, Fei
Xu, Xiaojin
Zhang, Dandan
Zhou, Bo
author_facet Dong, Bo
Xu, Xiaojin
Chen, Guoqing
Zhang, Dandan
Tang, Mingzhi
Xu, Fei
Liu, Xiaohong
Wang, Hua
Zhou, Bo
author_sort Dong, Bo
collection Repository of Agricultural Research Outputs (CGSpace)
description Conidiation patterning is evolutionarily complex and mechanism concerning conidiogenous cell differentiation remains largely unknown. Magnaporthe oryzae conidiates in a sympodial way and uses its conidia to infect host and disseminate blast disease. Arrestins are multifunctional proteins that modulate receptor down-regulation and scaffold components of intracellular trafficking routes. We here report an alpha-arrestin that regulates patterns of conidiation and contributes to pathogenicity in M. oryzae. We show that disruption of ARRDC1 generates mutants which produce conidia in an acropetal array and ARRDC1 significantly affects expression profile of CCA1, a virulence-related transcription factor required for conidiogenous cell differentiation. Although germ tubes normally develop appressoria, penetration peg formation is dramatically impaired and Δarrdc1 mutants are mostly nonpathogenic. Fluorescent analysis indicates that EGFP-ARRDC1 puncta are well colocalized with DsRed2-Atg8, and this distribution profile could not be altered in Δatg9 mutants, suggesting ARRDC1 enters into autophagic flux before autophagosome maturation. We propose that M. oryzae employs ARRDC1 to regulate specific receptors in response to conidiation-related signals for conidiogenous cell differentiation and utilize autophagosomes for desensitization of conidiogenous receptor, which transmits extracellular signal to the downstream elements of transcription factors. Our investigation extends novel significance of autophagy-associated alpha-arrestin signaling to fungal parasites.
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spelling CGSpace1652232024-12-19T14:12:08Z Autophagy-associated alpha-arrestin signaling is required for conidiogenous cell development in Magnaporthe oryzae Dong, Bo Xu, Xiaojin Chen, Guoqing Zhang, Dandan Tang, Mingzhi Xu, Fei Liu, Xiaohong Wang, Hua Zhou, Bo Conidiation patterning is evolutionarily complex and mechanism concerning conidiogenous cell differentiation remains largely unknown. Magnaporthe oryzae conidiates in a sympodial way and uses its conidia to infect host and disseminate blast disease. Arrestins are multifunctional proteins that modulate receptor down-regulation and scaffold components of intracellular trafficking routes. We here report an alpha-arrestin that regulates patterns of conidiation and contributes to pathogenicity in M. oryzae. We show that disruption of ARRDC1 generates mutants which produce conidia in an acropetal array and ARRDC1 significantly affects expression profile of CCA1, a virulence-related transcription factor required for conidiogenous cell differentiation. Although germ tubes normally develop appressoria, penetration peg formation is dramatically impaired and Δarrdc1 mutants are mostly nonpathogenic. Fluorescent analysis indicates that EGFP-ARRDC1 puncta are well colocalized with DsRed2-Atg8, and this distribution profile could not be altered in Δatg9 mutants, suggesting ARRDC1 enters into autophagic flux before autophagosome maturation. We propose that M. oryzae employs ARRDC1 to regulate specific receptors in response to conidiation-related signals for conidiogenous cell differentiation and utilize autophagosomes for desensitization of conidiogenous receptor, which transmits extracellular signal to the downstream elements of transcription factors. Our investigation extends novel significance of autophagy-associated alpha-arrestin signaling to fungal parasites. 2016-08-08 2024-12-19T12:54:50Z 2024-12-19T12:54:50Z Journal Article https://hdl.handle.net/10568/165223 en Open Access Springer Dong, Bo; Xu, Xiaojin; Chen, Guoqing; Zhang, Dandan; Tang, Mingzhi; Xu, Fei; Liu, Xiaohong; Wang, Hua and Zhou, Bo. 2016. Autophagy-associated alpha-arrestin signaling is required for conidiogenous cell development in Magnaporthe oryzae. Sci Rep, Volume 6, no. 1
spellingShingle Dong, Bo
Xu, Xiaojin
Chen, Guoqing
Zhang, Dandan
Tang, Mingzhi
Xu, Fei
Liu, Xiaohong
Wang, Hua
Zhou, Bo
Autophagy-associated alpha-arrestin signaling is required for conidiogenous cell development in Magnaporthe oryzae
title Autophagy-associated alpha-arrestin signaling is required for conidiogenous cell development in Magnaporthe oryzae
title_full Autophagy-associated alpha-arrestin signaling is required for conidiogenous cell development in Magnaporthe oryzae
title_fullStr Autophagy-associated alpha-arrestin signaling is required for conidiogenous cell development in Magnaporthe oryzae
title_full_unstemmed Autophagy-associated alpha-arrestin signaling is required for conidiogenous cell development in Magnaporthe oryzae
title_short Autophagy-associated alpha-arrestin signaling is required for conidiogenous cell development in Magnaporthe oryzae
title_sort autophagy associated alpha arrestin signaling is required for conidiogenous cell development in magnaporthe oryzae
url https://hdl.handle.net/10568/165223
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