Cargando…

Nitrate triggered phosphoproteome changes and a PIN2 phosphosite modulating root system architecture

Nitrate commands genome‐wide gene expression changes that impact metabolism, physiology, plant growth, and development. In an effort to identify new components involved in nitrate responses in plants, we analyze the Arabidopsis thaliana root phosphoproteome in response to nitrate treatments via liqu...

Descripción completa

Detalles Bibliográficos
Autores principales: Vega, Andrea, Fredes, Isabel, O’Brien, José, Shen, Zhouxin, Ötvös, Krisztina, Abualia, Rashed, Benkova, Eva, Briggs, Steven P, Gutiérrez, Rodrigo A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447600/
https://www.ncbi.nlm.nih.gov/pubmed/34357701
http://dx.doi.org/10.15252/embr.202051813
_version_ 1784569050731380736
author Vega, Andrea
Fredes, Isabel
O’Brien, José
Shen, Zhouxin
Ötvös, Krisztina
Abualia, Rashed
Benkova, Eva
Briggs, Steven P
Gutiérrez, Rodrigo A
author_facet Vega, Andrea
Fredes, Isabel
O’Brien, José
Shen, Zhouxin
Ötvös, Krisztina
Abualia, Rashed
Benkova, Eva
Briggs, Steven P
Gutiérrez, Rodrigo A
author_sort Vega, Andrea
collection PubMed
description Nitrate commands genome‐wide gene expression changes that impact metabolism, physiology, plant growth, and development. In an effort to identify new components involved in nitrate responses in plants, we analyze the Arabidopsis thaliana root phosphoproteome in response to nitrate treatments via liquid chromatography coupled to tandem mass spectrometry. 176 phosphoproteins show significant changes at 5 or 20 min after nitrate treatments. Proteins identified by 5 min include signaling components such as kinases or transcription factors. In contrast, by 20 min, proteins identified were associated with transporter activity or hormone metabolism functions, among others. The phosphorylation profile of NITRATE TRANSPORTER 1.1 (NRT1.1) mutant plants was significantly altered as compared to wild‐type plants, confirming its key role in nitrate signaling pathways that involves phosphorylation changes. Integrative bioinformatics analysis highlights auxin transport as an important mechanism modulated by nitrate signaling at the post‐translational level. We validated a new phosphorylation site in PIN2 and provide evidence that it functions in primary and lateral root growth responses to nitrate.
format Online
Article
Text
id pubmed-8447600
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-84476002021-09-27 Nitrate triggered phosphoproteome changes and a PIN2 phosphosite modulating root system architecture Vega, Andrea Fredes, Isabel O’Brien, José Shen, Zhouxin Ötvös, Krisztina Abualia, Rashed Benkova, Eva Briggs, Steven P Gutiérrez, Rodrigo A EMBO Rep Articles Nitrate commands genome‐wide gene expression changes that impact metabolism, physiology, plant growth, and development. In an effort to identify new components involved in nitrate responses in plants, we analyze the Arabidopsis thaliana root phosphoproteome in response to nitrate treatments via liquid chromatography coupled to tandem mass spectrometry. 176 phosphoproteins show significant changes at 5 or 20 min after nitrate treatments. Proteins identified by 5 min include signaling components such as kinases or transcription factors. In contrast, by 20 min, proteins identified were associated with transporter activity or hormone metabolism functions, among others. The phosphorylation profile of NITRATE TRANSPORTER 1.1 (NRT1.1) mutant plants was significantly altered as compared to wild‐type plants, confirming its key role in nitrate signaling pathways that involves phosphorylation changes. Integrative bioinformatics analysis highlights auxin transport as an important mechanism modulated by nitrate signaling at the post‐translational level. We validated a new phosphorylation site in PIN2 and provide evidence that it functions in primary and lateral root growth responses to nitrate. John Wiley and Sons Inc. 2021-08-06 2021-09-06 /pmc/articles/PMC8447600/ /pubmed/34357701 http://dx.doi.org/10.15252/embr.202051813 Text en © 2020 The Authors. Published under the terms of the CC BY NC ND 4.0 license 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 Articles
Vega, Andrea
Fredes, Isabel
O’Brien, José
Shen, Zhouxin
Ötvös, Krisztina
Abualia, Rashed
Benkova, Eva
Briggs, Steven P
Gutiérrez, Rodrigo A
Nitrate triggered phosphoproteome changes and a PIN2 phosphosite modulating root system architecture
title Nitrate triggered phosphoproteome changes and a PIN2 phosphosite modulating root system architecture
title_full Nitrate triggered phosphoproteome changes and a PIN2 phosphosite modulating root system architecture
title_fullStr Nitrate triggered phosphoproteome changes and a PIN2 phosphosite modulating root system architecture
title_full_unstemmed Nitrate triggered phosphoproteome changes and a PIN2 phosphosite modulating root system architecture
title_short Nitrate triggered phosphoproteome changes and a PIN2 phosphosite modulating root system architecture
title_sort nitrate triggered phosphoproteome changes and a pin2 phosphosite modulating root system architecture
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447600/
https://www.ncbi.nlm.nih.gov/pubmed/34357701
http://dx.doi.org/10.15252/embr.202051813
work_keys_str_mv AT vegaandrea nitratetriggeredphosphoproteomechangesandapin2phosphositemodulatingrootsystemarchitecture
AT fredesisabel nitratetriggeredphosphoproteomechangesandapin2phosphositemodulatingrootsystemarchitecture
AT obrienjose nitratetriggeredphosphoproteomechangesandapin2phosphositemodulatingrootsystemarchitecture
AT shenzhouxin nitratetriggeredphosphoproteomechangesandapin2phosphositemodulatingrootsystemarchitecture
AT otvoskrisztina nitratetriggeredphosphoproteomechangesandapin2phosphositemodulatingrootsystemarchitecture
AT abualiarashed nitratetriggeredphosphoproteomechangesandapin2phosphositemodulatingrootsystemarchitecture
AT benkovaeva nitratetriggeredphosphoproteomechangesandapin2phosphositemodulatingrootsystemarchitecture
AT briggsstevenp nitratetriggeredphosphoproteomechangesandapin2phosphositemodulatingrootsystemarchitecture
AT gutierrezrodrigoa nitratetriggeredphosphoproteomechangesandapin2phosphositemodulatingrootsystemarchitecture