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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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 |
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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 |
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