Cargando…
Serendipita bescii promotes winter wheat growth and modulates the host root transcriptome under phosphorus and nitrogen starvation
Serendipita vermifera ssp. bescii, hereafter referred to as S. bescii, is a root‐associated fungus that promotes plant growth in both its native switchgrass host and a variety of monocots and dicots. Winter wheat (Triticum aestivum L.), a dual‐purpose crop, used for both forage and grain production,...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247352/ https://www.ncbi.nlm.nih.gov/pubmed/32959463 http://dx.doi.org/10.1111/1462-2920.15242 |
_version_ | 1783716505728319488 |
---|---|
author | Ray, Prasun Guo, Yingqing Chi, Myoung‐Hwan Krom, Nick Saha, Malay C. Craven, Kelly D. |
author_facet | Ray, Prasun Guo, Yingqing Chi, Myoung‐Hwan Krom, Nick Saha, Malay C. Craven, Kelly D. |
author_sort | Ray, Prasun |
collection | PubMed |
description | Serendipita vermifera ssp. bescii, hereafter referred to as S. bescii, is a root‐associated fungus that promotes plant growth in both its native switchgrass host and a variety of monocots and dicots. Winter wheat (Triticum aestivum L.), a dual‐purpose crop, used for both forage and grain production, significantly contributes to the agricultural economies of the Southern Great Plains, USA. In this study, we investigated the influence of S. bescii on growth and transcriptome regulation of nitrogen (N) and phosphorus (P) metabolism in winter wheat. Serendipita bescii significantly improved lateral root growth and forage biomass under a limited N or P regime. Further, S. bescii activated sets of host genes regulating N and P starvation responses. These genes include, root‐specific auxin transport, strigolactone and gibberellin biosynthesis, degradation of phospholipids and biosynthesis of glycerolipid, downregulation of ammonium transport and nitrate assimilation, restriction of protein degradation by autophagy and subsequent N remobilization. All these genes are hypothesized to regulate acquisition, assimilation and remobilization of N and P. Based on transcriptional level gene regulation and physiological responses to N or P limitation, we suggest S. bescii plays a critical role in modulating stress imposed by limitation of these two critical nutrients in winter wheat. |
format | Online Article Text |
id | pubmed-8247352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82473522021-07-02 Serendipita bescii promotes winter wheat growth and modulates the host root transcriptome under phosphorus and nitrogen starvation Ray, Prasun Guo, Yingqing Chi, Myoung‐Hwan Krom, Nick Saha, Malay C. Craven, Kelly D. Environ Microbiol Research Articles Serendipita vermifera ssp. bescii, hereafter referred to as S. bescii, is a root‐associated fungus that promotes plant growth in both its native switchgrass host and a variety of monocots and dicots. Winter wheat (Triticum aestivum L.), a dual‐purpose crop, used for both forage and grain production, significantly contributes to the agricultural economies of the Southern Great Plains, USA. In this study, we investigated the influence of S. bescii on growth and transcriptome regulation of nitrogen (N) and phosphorus (P) metabolism in winter wheat. Serendipita bescii significantly improved lateral root growth and forage biomass under a limited N or P regime. Further, S. bescii activated sets of host genes regulating N and P starvation responses. These genes include, root‐specific auxin transport, strigolactone and gibberellin biosynthesis, degradation of phospholipids and biosynthesis of glycerolipid, downregulation of ammonium transport and nitrate assimilation, restriction of protein degradation by autophagy and subsequent N remobilization. All these genes are hypothesized to regulate acquisition, assimilation and remobilization of N and P. Based on transcriptional level gene regulation and physiological responses to N or P limitation, we suggest S. bescii plays a critical role in modulating stress imposed by limitation of these two critical nutrients in winter wheat. John Wiley & Sons, Inc. 2020-10-05 2021-04 /pmc/articles/PMC8247352/ /pubmed/32959463 http://dx.doi.org/10.1111/1462-2920.15242 Text en © 2020 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Ray, Prasun Guo, Yingqing Chi, Myoung‐Hwan Krom, Nick Saha, Malay C. Craven, Kelly D. Serendipita bescii promotes winter wheat growth and modulates the host root transcriptome under phosphorus and nitrogen starvation |
title |
Serendipita bescii promotes winter wheat growth and modulates the host root transcriptome under phosphorus and nitrogen starvation |
title_full |
Serendipita bescii promotes winter wheat growth and modulates the host root transcriptome under phosphorus and nitrogen starvation |
title_fullStr |
Serendipita bescii promotes winter wheat growth and modulates the host root transcriptome under phosphorus and nitrogen starvation |
title_full_unstemmed |
Serendipita bescii promotes winter wheat growth and modulates the host root transcriptome under phosphorus and nitrogen starvation |
title_short |
Serendipita bescii promotes winter wheat growth and modulates the host root transcriptome under phosphorus and nitrogen starvation |
title_sort | serendipita bescii promotes winter wheat growth and modulates the host root transcriptome under phosphorus and nitrogen starvation |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247352/ https://www.ncbi.nlm.nih.gov/pubmed/32959463 http://dx.doi.org/10.1111/1462-2920.15242 |
work_keys_str_mv | AT rayprasun serendipitabesciipromoteswinterwheatgrowthandmodulatesthehostroottranscriptomeunderphosphorusandnitrogenstarvation AT guoyingqing serendipitabesciipromoteswinterwheatgrowthandmodulatesthehostroottranscriptomeunderphosphorusandnitrogenstarvation AT chimyounghwan serendipitabesciipromoteswinterwheatgrowthandmodulatesthehostroottranscriptomeunderphosphorusandnitrogenstarvation AT kromnick serendipitabesciipromoteswinterwheatgrowthandmodulatesthehostroottranscriptomeunderphosphorusandnitrogenstarvation AT sahamalayc serendipitabesciipromoteswinterwheatgrowthandmodulatesthehostroottranscriptomeunderphosphorusandnitrogenstarvation AT cravenkellyd serendipitabesciipromoteswinterwheatgrowthandmodulatesthehostroottranscriptomeunderphosphorusandnitrogenstarvation |