Cargando…

PHOSPHATE STARVATION RESPONSE transcription factors enable arbuscular mycorrhiza symbiosis

Arbuscular mycorrhiza (AM) is a widespread symbiosis between roots of the majority of land plants and Glomeromycotina fungi. AM is important for ecosystem health and functioning as the fungi critically support plant performance by providing essential mineral nutrients, particularly the poorly access...

Descripción completa

Detalles Bibliográficos
Autores principales: Das, Debatosh, Paries, Michael, Hobecker, Karen, Gigl, Michael, Dawid, Corinna, Lam, Hon-Ming, Zhang, Jianhua, Chen, Moxian, Gutjahr, Caroline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789775/
https://www.ncbi.nlm.nih.gov/pubmed/35078978
http://dx.doi.org/10.1038/s41467-022-27976-8
_version_ 1784639848132378624
author Das, Debatosh
Paries, Michael
Hobecker, Karen
Gigl, Michael
Dawid, Corinna
Lam, Hon-Ming
Zhang, Jianhua
Chen, Moxian
Gutjahr, Caroline
author_facet Das, Debatosh
Paries, Michael
Hobecker, Karen
Gigl, Michael
Dawid, Corinna
Lam, Hon-Ming
Zhang, Jianhua
Chen, Moxian
Gutjahr, Caroline
author_sort Das, Debatosh
collection PubMed
description Arbuscular mycorrhiza (AM) is a widespread symbiosis between roots of the majority of land plants and Glomeromycotina fungi. AM is important for ecosystem health and functioning as the fungi critically support plant performance by providing essential mineral nutrients, particularly the poorly accessible phosphate, in exchange for organic carbon. AM fungi colonize the inside of roots and this is promoted at low but inhibited at high plant phosphate status, while the mechanistic basis for this phosphate-dependence remained obscure. Here we demonstrate that a major transcriptional regulator of phosphate starvation responses in rice PHOSPHATE STARVATION RESPONSE 2 (PHR2) regulates AM. Root colonization of phr2 mutants is drastically reduced, and PHR2 is required for root colonization, mycorrhizal phosphate uptake, and yield increase in field soil. PHR2 promotes AM by targeting genes required for pre-contact signaling, root colonization, and AM function. Thus, this important symbiosis is directly wired to the PHR2-controlled plant phosphate starvation response.
format Online
Article
Text
id pubmed-8789775
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-87897752022-02-07 PHOSPHATE STARVATION RESPONSE transcription factors enable arbuscular mycorrhiza symbiosis Das, Debatosh Paries, Michael Hobecker, Karen Gigl, Michael Dawid, Corinna Lam, Hon-Ming Zhang, Jianhua Chen, Moxian Gutjahr, Caroline Nat Commun Article Arbuscular mycorrhiza (AM) is a widespread symbiosis between roots of the majority of land plants and Glomeromycotina fungi. AM is important for ecosystem health and functioning as the fungi critically support plant performance by providing essential mineral nutrients, particularly the poorly accessible phosphate, in exchange for organic carbon. AM fungi colonize the inside of roots and this is promoted at low but inhibited at high plant phosphate status, while the mechanistic basis for this phosphate-dependence remained obscure. Here we demonstrate that a major transcriptional regulator of phosphate starvation responses in rice PHOSPHATE STARVATION RESPONSE 2 (PHR2) regulates AM. Root colonization of phr2 mutants is drastically reduced, and PHR2 is required for root colonization, mycorrhizal phosphate uptake, and yield increase in field soil. PHR2 promotes AM by targeting genes required for pre-contact signaling, root colonization, and AM function. Thus, this important symbiosis is directly wired to the PHR2-controlled plant phosphate starvation response. Nature Publishing Group UK 2022-01-25 /pmc/articles/PMC8789775/ /pubmed/35078978 http://dx.doi.org/10.1038/s41467-022-27976-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Das, Debatosh
Paries, Michael
Hobecker, Karen
Gigl, Michael
Dawid, Corinna
Lam, Hon-Ming
Zhang, Jianhua
Chen, Moxian
Gutjahr, Caroline
PHOSPHATE STARVATION RESPONSE transcription factors enable arbuscular mycorrhiza symbiosis
title PHOSPHATE STARVATION RESPONSE transcription factors enable arbuscular mycorrhiza symbiosis
title_full PHOSPHATE STARVATION RESPONSE transcription factors enable arbuscular mycorrhiza symbiosis
title_fullStr PHOSPHATE STARVATION RESPONSE transcription factors enable arbuscular mycorrhiza symbiosis
title_full_unstemmed PHOSPHATE STARVATION RESPONSE transcription factors enable arbuscular mycorrhiza symbiosis
title_short PHOSPHATE STARVATION RESPONSE transcription factors enable arbuscular mycorrhiza symbiosis
title_sort phosphate starvation response transcription factors enable arbuscular mycorrhiza symbiosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789775/
https://www.ncbi.nlm.nih.gov/pubmed/35078978
http://dx.doi.org/10.1038/s41467-022-27976-8
work_keys_str_mv AT dasdebatosh phosphatestarvationresponsetranscriptionfactorsenablearbuscularmycorrhizasymbiosis
AT pariesmichael phosphatestarvationresponsetranscriptionfactorsenablearbuscularmycorrhizasymbiosis
AT hobeckerkaren phosphatestarvationresponsetranscriptionfactorsenablearbuscularmycorrhizasymbiosis
AT giglmichael phosphatestarvationresponsetranscriptionfactorsenablearbuscularmycorrhizasymbiosis
AT dawidcorinna phosphatestarvationresponsetranscriptionfactorsenablearbuscularmycorrhizasymbiosis
AT lamhonming phosphatestarvationresponsetranscriptionfactorsenablearbuscularmycorrhizasymbiosis
AT zhangjianhua phosphatestarvationresponsetranscriptionfactorsenablearbuscularmycorrhizasymbiosis
AT chenmoxian phosphatestarvationresponsetranscriptionfactorsenablearbuscularmycorrhizasymbiosis
AT gutjahrcaroline phosphatestarvationresponsetranscriptionfactorsenablearbuscularmycorrhizasymbiosis