Cargando…

Light-triggered and phosphorylation-dependent 14-3-3 association with NON-PHOTOTROPIC HYPOCOTYL 3 is required for hypocotyl phototropism

NON-PHOTOTROPIC HYPOCOTYL 3 (NPH3) is a key component of the auxin-dependent plant phototropic growth response. We report that NPH3 directly binds polyacidic phospholipids, required for plasma membrane association in darkness. We further demonstrate that blue light induces an immediate phosphorylati...

Descripción completa

Detalles Bibliográficos
Autores principales: Reuter, Lea, Schmidt, Tanja, Manishankar, Prabha, Throm, Christian, Keicher, Jutta, Bock, Andrea, Droste-Borel, Irina, Oecking, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531446/
https://www.ncbi.nlm.nih.gov/pubmed/34675219
http://dx.doi.org/10.1038/s41467-021-26332-6
_version_ 1784586860127846400
author Reuter, Lea
Schmidt, Tanja
Manishankar, Prabha
Throm, Christian
Keicher, Jutta
Bock, Andrea
Droste-Borel, Irina
Oecking, Claudia
author_facet Reuter, Lea
Schmidt, Tanja
Manishankar, Prabha
Throm, Christian
Keicher, Jutta
Bock, Andrea
Droste-Borel, Irina
Oecking, Claudia
author_sort Reuter, Lea
collection PubMed
description NON-PHOTOTROPIC HYPOCOTYL 3 (NPH3) is a key component of the auxin-dependent plant phototropic growth response. We report that NPH3 directly binds polyacidic phospholipids, required for plasma membrane association in darkness. We further demonstrate that blue light induces an immediate phosphorylation of a C-terminal 14-3-3 binding motif in NPH3. Subsequent association of 14-3-3 proteins is causal for the light-induced release of NPH3 from the membrane and accompanied by NPH3 dephosphorylation. In the cytosol, NPH3 dynamically transitions into membraneless condensate-like structures. The dephosphorylated state of the 14-3-3 binding site and NPH3 membrane recruitment are recoverable in darkness. NPH3 variants that constitutively localize either to the membrane or to condensates are non-functional, revealing a fundamental role of the 14-3-3 mediated dynamic change in NPH3 localization for auxin-dependent phototropism. This regulatory mechanism might be of general nature, given that several members of the NPH3-like family interact with 14-3-3 via a C-terminal motif.
format Online
Article
Text
id pubmed-8531446
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-85314462021-11-15 Light-triggered and phosphorylation-dependent 14-3-3 association with NON-PHOTOTROPIC HYPOCOTYL 3 is required for hypocotyl phototropism Reuter, Lea Schmidt, Tanja Manishankar, Prabha Throm, Christian Keicher, Jutta Bock, Andrea Droste-Borel, Irina Oecking, Claudia Nat Commun Article NON-PHOTOTROPIC HYPOCOTYL 3 (NPH3) is a key component of the auxin-dependent plant phototropic growth response. We report that NPH3 directly binds polyacidic phospholipids, required for plasma membrane association in darkness. We further demonstrate that blue light induces an immediate phosphorylation of a C-terminal 14-3-3 binding motif in NPH3. Subsequent association of 14-3-3 proteins is causal for the light-induced release of NPH3 from the membrane and accompanied by NPH3 dephosphorylation. In the cytosol, NPH3 dynamically transitions into membraneless condensate-like structures. The dephosphorylated state of the 14-3-3 binding site and NPH3 membrane recruitment are recoverable in darkness. NPH3 variants that constitutively localize either to the membrane or to condensates are non-functional, revealing a fundamental role of the 14-3-3 mediated dynamic change in NPH3 localization for auxin-dependent phototropism. This regulatory mechanism might be of general nature, given that several members of the NPH3-like family interact with 14-3-3 via a C-terminal motif. Nature Publishing Group UK 2021-10-21 /pmc/articles/PMC8531446/ /pubmed/34675219 http://dx.doi.org/10.1038/s41467-021-26332-6 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
Reuter, Lea
Schmidt, Tanja
Manishankar, Prabha
Throm, Christian
Keicher, Jutta
Bock, Andrea
Droste-Borel, Irina
Oecking, Claudia
Light-triggered and phosphorylation-dependent 14-3-3 association with NON-PHOTOTROPIC HYPOCOTYL 3 is required for hypocotyl phototropism
title Light-triggered and phosphorylation-dependent 14-3-3 association with NON-PHOTOTROPIC HYPOCOTYL 3 is required for hypocotyl phototropism
title_full Light-triggered and phosphorylation-dependent 14-3-3 association with NON-PHOTOTROPIC HYPOCOTYL 3 is required for hypocotyl phototropism
title_fullStr Light-triggered and phosphorylation-dependent 14-3-3 association with NON-PHOTOTROPIC HYPOCOTYL 3 is required for hypocotyl phototropism
title_full_unstemmed Light-triggered and phosphorylation-dependent 14-3-3 association with NON-PHOTOTROPIC HYPOCOTYL 3 is required for hypocotyl phototropism
title_short Light-triggered and phosphorylation-dependent 14-3-3 association with NON-PHOTOTROPIC HYPOCOTYL 3 is required for hypocotyl phototropism
title_sort light-triggered and phosphorylation-dependent 14-3-3 association with non-phototropic hypocotyl 3 is required for hypocotyl phototropism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8531446/
https://www.ncbi.nlm.nih.gov/pubmed/34675219
http://dx.doi.org/10.1038/s41467-021-26332-6
work_keys_str_mv AT reuterlea lighttriggeredandphosphorylationdependent1433associationwithnonphototropichypocotyl3isrequiredforhypocotylphototropism
AT schmidttanja lighttriggeredandphosphorylationdependent1433associationwithnonphototropichypocotyl3isrequiredforhypocotylphototropism
AT manishankarprabha lighttriggeredandphosphorylationdependent1433associationwithnonphototropichypocotyl3isrequiredforhypocotylphototropism
AT thromchristian lighttriggeredandphosphorylationdependent1433associationwithnonphototropichypocotyl3isrequiredforhypocotylphototropism
AT keicherjutta lighttriggeredandphosphorylationdependent1433associationwithnonphototropichypocotyl3isrequiredforhypocotylphototropism
AT bockandrea lighttriggeredandphosphorylationdependent1433associationwithnonphototropichypocotyl3isrequiredforhypocotylphototropism
AT drosteborelirina lighttriggeredandphosphorylationdependent1433associationwithnonphototropichypocotyl3isrequiredforhypocotylphototropism
AT oeckingclaudia lighttriggeredandphosphorylationdependent1433associationwithnonphototropichypocotyl3isrequiredforhypocotylphototropism