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Regulation of plant phototropic growth by NPH3/RPT2-like substrate phosphorylation and 14-3-3 binding

Polarity underlies all directional growth responses in plants including growth towards the light (phototropism). The plasma-membrane associated protein, NON-PHOTOTROPIC HYPOCOTYL 3 (NPH3) is a key determinant of phototropic growth which is regulated by phototropin (phot) AGC kinases. Here we demonst...

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Autores principales: Sullivan, Stuart, Waksman, Thomas, Paliogianni, Dimitra, Henderson, Louise, Lütkemeyer, Melanie, Suetsugu, Noriyuki, Christie, John M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531357/
https://www.ncbi.nlm.nih.gov/pubmed/34675214
http://dx.doi.org/10.1038/s41467-021-26333-5
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author Sullivan, Stuart
Waksman, Thomas
Paliogianni, Dimitra
Henderson, Louise
Lütkemeyer, Melanie
Suetsugu, Noriyuki
Christie, John M.
author_facet Sullivan, Stuart
Waksman, Thomas
Paliogianni, Dimitra
Henderson, Louise
Lütkemeyer, Melanie
Suetsugu, Noriyuki
Christie, John M.
author_sort Sullivan, Stuart
collection PubMed
description Polarity underlies all directional growth responses in plants including growth towards the light (phototropism). The plasma-membrane associated protein, NON-PHOTOTROPIC HYPOCOTYL 3 (NPH3) is a key determinant of phototropic growth which is regulated by phototropin (phot) AGC kinases. Here we demonstrate that NPH3 is directly phosphorylated by phot1 within a conserved C-terminal consensus sequence (RxS) that is necessary to promote phototropism and petiole positioning in Arabidopsis. RxS phosphorylation also triggers 14-3-3 binding combined with changes in NPH3 phosphorylation and localisation status. Mutants of NPH3 that are unable to bind or constitutively bind 14-3-3 s show compromised functionality consistent with a model where phototropic curvature is established by signalling outputs arising from a gradient of NPH3 RxS phosphorylation across the stem. Our findings therefore establish that NPH3/RPT2-Like (NRL) proteins are phosphorylation targets for plant AGC kinases. Moreover, RxS phosphorylation is conserved in other members of the NRL family, suggesting a common mechanism of regulating plant growth to the prevailing light environment.
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spelling pubmed-85313572021-10-22 Regulation of plant phototropic growth by NPH3/RPT2-like substrate phosphorylation and 14-3-3 binding Sullivan, Stuart Waksman, Thomas Paliogianni, Dimitra Henderson, Louise Lütkemeyer, Melanie Suetsugu, Noriyuki Christie, John M. Nat Commun Article Polarity underlies all directional growth responses in plants including growth towards the light (phototropism). The plasma-membrane associated protein, NON-PHOTOTROPIC HYPOCOTYL 3 (NPH3) is a key determinant of phototropic growth which is regulated by phototropin (phot) AGC kinases. Here we demonstrate that NPH3 is directly phosphorylated by phot1 within a conserved C-terminal consensus sequence (RxS) that is necessary to promote phototropism and petiole positioning in Arabidopsis. RxS phosphorylation also triggers 14-3-3 binding combined with changes in NPH3 phosphorylation and localisation status. Mutants of NPH3 that are unable to bind or constitutively bind 14-3-3 s show compromised functionality consistent with a model where phototropic curvature is established by signalling outputs arising from a gradient of NPH3 RxS phosphorylation across the stem. Our findings therefore establish that NPH3/RPT2-Like (NRL) proteins are phosphorylation targets for plant AGC kinases. Moreover, RxS phosphorylation is conserved in other members of the NRL family, suggesting a common mechanism of regulating plant growth to the prevailing light environment. Nature Publishing Group UK 2021-10-21 /pmc/articles/PMC8531357/ /pubmed/34675214 http://dx.doi.org/10.1038/s41467-021-26333-5 Text en © The Author(s) 2021 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
Sullivan, Stuart
Waksman, Thomas
Paliogianni, Dimitra
Henderson, Louise
Lütkemeyer, Melanie
Suetsugu, Noriyuki
Christie, John M.
Regulation of plant phototropic growth by NPH3/RPT2-like substrate phosphorylation and 14-3-3 binding
title Regulation of plant phototropic growth by NPH3/RPT2-like substrate phosphorylation and 14-3-3 binding
title_full Regulation of plant phototropic growth by NPH3/RPT2-like substrate phosphorylation and 14-3-3 binding
title_fullStr Regulation of plant phototropic growth by NPH3/RPT2-like substrate phosphorylation and 14-3-3 binding
title_full_unstemmed Regulation of plant phototropic growth by NPH3/RPT2-like substrate phosphorylation and 14-3-3 binding
title_short Regulation of plant phototropic growth by NPH3/RPT2-like substrate phosphorylation and 14-3-3 binding
title_sort regulation of plant phototropic growth by nph3/rpt2-like substrate phosphorylation and 14-3-3 binding
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531357/
https://www.ncbi.nlm.nih.gov/pubmed/34675214
http://dx.doi.org/10.1038/s41467-021-26333-5
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