Cargando…

A transcriptional activator from Rhizophagus irregularis regulates phosphate uptake and homeostasis in AM symbiosis during phosphorous starvation

INTRODUCTION: Phosphorus (P) is one of the most important nutrient elements for plant growth and development. Under P starvation, arbuscular mycorrhizal (AM) fungi can promote phosphate (Pi) uptake and homeostasis within host plants. However, the underlying mechanisms by which AM fungal symbiont reg...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Shuyuan, Nie, Yuying, Fan, Xiaoning, Wei, Wei, Chen, Hui, Xie, Xianan, Tang, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9895418/
https://www.ncbi.nlm.nih.gov/pubmed/36741887
http://dx.doi.org/10.3389/fmicb.2022.1114089
_version_ 1784881903618228224
author Zhang, Shuyuan
Nie, Yuying
Fan, Xiaoning
Wei, Wei
Chen, Hui
Xie, Xianan
Tang, Ming
author_facet Zhang, Shuyuan
Nie, Yuying
Fan, Xiaoning
Wei, Wei
Chen, Hui
Xie, Xianan
Tang, Ming
author_sort Zhang, Shuyuan
collection PubMed
description INTRODUCTION: Phosphorus (P) is one of the most important nutrient elements for plant growth and development. Under P starvation, arbuscular mycorrhizal (AM) fungi can promote phosphate (Pi) uptake and homeostasis within host plants. However, the underlying mechanisms by which AM fungal symbiont regulates the AM symbiotic Pi acquisition from soil under P starvation are largely unknown. Here, we identify a HLH domain containing transcription factor RiPho4 from Rhizophagus irregularis. METHODS: To investigate the biological functions of the RiPho4, we combined the subcellular localization and Yeast One-Hybrid (Y1H) experiments in yeasts with gene expression and virus-induced gene silencing approach during AM symbiosis. RESULTS: The approach during AM symbiosis. The results indicated that RiPho4 encodes a conserved transcription factor among different fungi and is induced during the in planta phase. The transcription of RiPho4 is significantly up-regulated by P starvation. The subcellular localization analysis revealed that RiPho4 is located in the nuclei of yeast cells during P starvation. Moreover, knock-down of RiPho4 inhibits the arbuscule development and mycorrhizal Pi uptake under low Pi conditions. Importantly, RiPho4 can positively regulate the downstream components of the phosphate (PHO) pathway in R. irregularis. DISCUSSION: In summary, these new findings reveal that RiPho4 acts as a transcriptional activator in AM fungus to maintain arbuscule development and regulate Pi uptake and homeostasis in the AM symbiosis during Pi starvation.
format Online
Article
Text
id pubmed-9895418
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-98954182023-02-04 A transcriptional activator from Rhizophagus irregularis regulates phosphate uptake and homeostasis in AM symbiosis during phosphorous starvation Zhang, Shuyuan Nie, Yuying Fan, Xiaoning Wei, Wei Chen, Hui Xie, Xianan Tang, Ming Front Microbiol Microbiology INTRODUCTION: Phosphorus (P) is one of the most important nutrient elements for plant growth and development. Under P starvation, arbuscular mycorrhizal (AM) fungi can promote phosphate (Pi) uptake and homeostasis within host plants. However, the underlying mechanisms by which AM fungal symbiont regulates the AM symbiotic Pi acquisition from soil under P starvation are largely unknown. Here, we identify a HLH domain containing transcription factor RiPho4 from Rhizophagus irregularis. METHODS: To investigate the biological functions of the RiPho4, we combined the subcellular localization and Yeast One-Hybrid (Y1H) experiments in yeasts with gene expression and virus-induced gene silencing approach during AM symbiosis. RESULTS: The approach during AM symbiosis. The results indicated that RiPho4 encodes a conserved transcription factor among different fungi and is induced during the in planta phase. The transcription of RiPho4 is significantly up-regulated by P starvation. The subcellular localization analysis revealed that RiPho4 is located in the nuclei of yeast cells during P starvation. Moreover, knock-down of RiPho4 inhibits the arbuscule development and mycorrhizal Pi uptake under low Pi conditions. Importantly, RiPho4 can positively regulate the downstream components of the phosphate (PHO) pathway in R. irregularis. DISCUSSION: In summary, these new findings reveal that RiPho4 acts as a transcriptional activator in AM fungus to maintain arbuscule development and regulate Pi uptake and homeostasis in the AM symbiosis during Pi starvation. Frontiers Media S.A. 2023-01-20 /pmc/articles/PMC9895418/ /pubmed/36741887 http://dx.doi.org/10.3389/fmicb.2022.1114089 Text en Copyright © 2023 Zhang, Nie, Fan, Wei, Chen, Xie and Tang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Zhang, Shuyuan
Nie, Yuying
Fan, Xiaoning
Wei, Wei
Chen, Hui
Xie, Xianan
Tang, Ming
A transcriptional activator from Rhizophagus irregularis regulates phosphate uptake and homeostasis in AM symbiosis during phosphorous starvation
title A transcriptional activator from Rhizophagus irregularis regulates phosphate uptake and homeostasis in AM symbiosis during phosphorous starvation
title_full A transcriptional activator from Rhizophagus irregularis regulates phosphate uptake and homeostasis in AM symbiosis during phosphorous starvation
title_fullStr A transcriptional activator from Rhizophagus irregularis regulates phosphate uptake and homeostasis in AM symbiosis during phosphorous starvation
title_full_unstemmed A transcriptional activator from Rhizophagus irregularis regulates phosphate uptake and homeostasis in AM symbiosis during phosphorous starvation
title_short A transcriptional activator from Rhizophagus irregularis regulates phosphate uptake and homeostasis in AM symbiosis during phosphorous starvation
title_sort transcriptional activator from rhizophagus irregularis regulates phosphate uptake and homeostasis in am symbiosis during phosphorous starvation
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9895418/
https://www.ncbi.nlm.nih.gov/pubmed/36741887
http://dx.doi.org/10.3389/fmicb.2022.1114089
work_keys_str_mv AT zhangshuyuan atranscriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT nieyuying atranscriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT fanxiaoning atranscriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT weiwei atranscriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT chenhui atranscriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT xiexianan atranscriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT tangming atranscriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT zhangshuyuan transcriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT nieyuying transcriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT fanxiaoning transcriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT weiwei transcriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT chenhui transcriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT xiexianan transcriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation
AT tangming transcriptionalactivatorfromrhizophagusirregularisregulatesphosphateuptakeandhomeostasisinamsymbiosisduringphosphorousstarvation