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Light triggers PILS-dependent reduction in nuclear auxin signalling for growth transition
The phytohormone auxin induces or represses growth depending on its concentration and the underlying tissue type. However, it remains unknown how auxin signalling is modulated to allow tissues transiting between repression and promotion of growth. Here we used apical hook development as a model for...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524181/ https://www.ncbi.nlm.nih.gov/pubmed/28714973 http://dx.doi.org/10.1038/nplants.2017.105 |
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author | Béziat, Chloé Barbez, Elke Feraru, Mugurel I. Lucyshyn, Doris Kleine-Vehn, Jürgen |
author_facet | Béziat, Chloé Barbez, Elke Feraru, Mugurel I. Lucyshyn, Doris Kleine-Vehn, Jürgen |
author_sort | Béziat, Chloé |
collection | PubMed |
description | The phytohormone auxin induces or represses growth depending on its concentration and the underlying tissue type. However, it remains unknown how auxin signalling is modulated to allow tissues transiting between repression and promotion of growth. Here we used apical hook development as a model for growth transitions in plants. A PIN-FORMED (PIN)-dependent intercellular auxin transport module defines an auxin maximum that is causal for growth repression during the formation of the apical hook. Our data illustrates that growth transition for apical hook opening is largely independent of this PIN module, but requires the PIN-LIKES (PILS) putative auxin carriers at the endoplasmic reticulum. PILS proteins reduce nuclear auxin signalling in the apical hook, leading to the de-repression of growth and the onset of hook opening. We also show that the phytochrome (phy) B-reliant light-signalling pathway directly regulates PILS gene activity, thereby enabling light perception to repress nuclear auxin signalling and to control growth. We propose a novel mechanism, in which PILS proteins allow external signals to alter tissue sensitivity to auxin, defining differential growth rates. |
format | Online Article Text |
id | pubmed-5524181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-55241812018-01-17 Light triggers PILS-dependent reduction in nuclear auxin signalling for growth transition Béziat, Chloé Barbez, Elke Feraru, Mugurel I. Lucyshyn, Doris Kleine-Vehn, Jürgen Nat Plants Article The phytohormone auxin induces or represses growth depending on its concentration and the underlying tissue type. However, it remains unknown how auxin signalling is modulated to allow tissues transiting between repression and promotion of growth. Here we used apical hook development as a model for growth transitions in plants. A PIN-FORMED (PIN)-dependent intercellular auxin transport module defines an auxin maximum that is causal for growth repression during the formation of the apical hook. Our data illustrates that growth transition for apical hook opening is largely independent of this PIN module, but requires the PIN-LIKES (PILS) putative auxin carriers at the endoplasmic reticulum. PILS proteins reduce nuclear auxin signalling in the apical hook, leading to the de-repression of growth and the onset of hook opening. We also show that the phytochrome (phy) B-reliant light-signalling pathway directly regulates PILS gene activity, thereby enabling light perception to repress nuclear auxin signalling and to control growth. We propose a novel mechanism, in which PILS proteins allow external signals to alter tissue sensitivity to auxin, defining differential growth rates. 2017-07-17 /pmc/articles/PMC5524181/ /pubmed/28714973 http://dx.doi.org/10.1038/nplants.2017.105 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Béziat, Chloé Barbez, Elke Feraru, Mugurel I. Lucyshyn, Doris Kleine-Vehn, Jürgen Light triggers PILS-dependent reduction in nuclear auxin signalling for growth transition |
title | Light triggers PILS-dependent reduction in nuclear auxin signalling for growth transition |
title_full | Light triggers PILS-dependent reduction in nuclear auxin signalling for growth transition |
title_fullStr | Light triggers PILS-dependent reduction in nuclear auxin signalling for growth transition |
title_full_unstemmed | Light triggers PILS-dependent reduction in nuclear auxin signalling for growth transition |
title_short | Light triggers PILS-dependent reduction in nuclear auxin signalling for growth transition |
title_sort | light triggers pils-dependent reduction in nuclear auxin signalling for growth transition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524181/ https://www.ncbi.nlm.nih.gov/pubmed/28714973 http://dx.doi.org/10.1038/nplants.2017.105 |
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