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Guard cells control hypocotyl elongation through HXK1, HY5, and PIF4

The hypocotyls of germinating seedlings elongate in a search for light to enable autotrophic sugar production. Upon exposure to light, photoreceptors that are activated by blue and red light halt elongation by preventing the degradation of the hypocotyl-elongation inhibitor HY5 and by inhibiting the...

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Autores principales: Kelly, Gilor, Brandsma, Danja, Egbaria, Aiman, Stein, Ofer, Doron-Faigenboim, Adi, Lugassi, Nitsan, Belausov, Eduard, Zemach, Hanita, Shaya, Felix, Carmi, Nir, Sade, Nir, Granot, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217561/
https://www.ncbi.nlm.nih.gov/pubmed/34155329
http://dx.doi.org/10.1038/s42003-021-02283-y
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author Kelly, Gilor
Brandsma, Danja
Egbaria, Aiman
Stein, Ofer
Doron-Faigenboim, Adi
Lugassi, Nitsan
Belausov, Eduard
Zemach, Hanita
Shaya, Felix
Carmi, Nir
Sade, Nir
Granot, David
author_facet Kelly, Gilor
Brandsma, Danja
Egbaria, Aiman
Stein, Ofer
Doron-Faigenboim, Adi
Lugassi, Nitsan
Belausov, Eduard
Zemach, Hanita
Shaya, Felix
Carmi, Nir
Sade, Nir
Granot, David
author_sort Kelly, Gilor
collection PubMed
description The hypocotyls of germinating seedlings elongate in a search for light to enable autotrophic sugar production. Upon exposure to light, photoreceptors that are activated by blue and red light halt elongation by preventing the degradation of the hypocotyl-elongation inhibitor HY5 and by inhibiting the activity of the elongation-promoting transcription factors PIFs. The question of how sugar affects hypocotyl elongation and which cell types stimulate and stop that elongation remains unresolved. We found that overexpression of a sugar sensor, Arabidopsis hexokinase 1 (HXK1), in guard cells promotes hypocotyl elongation under white and blue light through PIF4. Furthermore, expression of PIF4 in guard cells is sufficient to promote hypocotyl elongation in the light, while expression of HY5 in guard cells is sufficient to inhibit the elongation of the hy5 mutant and the elongation stimulated by HXK1. HY5 exits the guard cells and inhibits hypocotyl elongation, but is degraded in the dark. We also show that the inhibition of hypocotyl elongation by guard cells’ HY5 involves auto-activation of HY5 expression in other tissues. It appears that guard cells are capable of coordinating hypocotyl elongation and that sugar and HXK1 have the opposite effect of light on hypocotyl elongation, converging at PIF4.
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spelling pubmed-82175612021-07-09 Guard cells control hypocotyl elongation through HXK1, HY5, and PIF4 Kelly, Gilor Brandsma, Danja Egbaria, Aiman Stein, Ofer Doron-Faigenboim, Adi Lugassi, Nitsan Belausov, Eduard Zemach, Hanita Shaya, Felix Carmi, Nir Sade, Nir Granot, David Commun Biol Article The hypocotyls of germinating seedlings elongate in a search for light to enable autotrophic sugar production. Upon exposure to light, photoreceptors that are activated by blue and red light halt elongation by preventing the degradation of the hypocotyl-elongation inhibitor HY5 and by inhibiting the activity of the elongation-promoting transcription factors PIFs. The question of how sugar affects hypocotyl elongation and which cell types stimulate and stop that elongation remains unresolved. We found that overexpression of a sugar sensor, Arabidopsis hexokinase 1 (HXK1), in guard cells promotes hypocotyl elongation under white and blue light through PIF4. Furthermore, expression of PIF4 in guard cells is sufficient to promote hypocotyl elongation in the light, while expression of HY5 in guard cells is sufficient to inhibit the elongation of the hy5 mutant and the elongation stimulated by HXK1. HY5 exits the guard cells and inhibits hypocotyl elongation, but is degraded in the dark. We also show that the inhibition of hypocotyl elongation by guard cells’ HY5 involves auto-activation of HY5 expression in other tissues. It appears that guard cells are capable of coordinating hypocotyl elongation and that sugar and HXK1 have the opposite effect of light on hypocotyl elongation, converging at PIF4. Nature Publishing Group UK 2021-06-21 /pmc/articles/PMC8217561/ /pubmed/34155329 http://dx.doi.org/10.1038/s42003-021-02283-y 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
Kelly, Gilor
Brandsma, Danja
Egbaria, Aiman
Stein, Ofer
Doron-Faigenboim, Adi
Lugassi, Nitsan
Belausov, Eduard
Zemach, Hanita
Shaya, Felix
Carmi, Nir
Sade, Nir
Granot, David
Guard cells control hypocotyl elongation through HXK1, HY5, and PIF4
title Guard cells control hypocotyl elongation through HXK1, HY5, and PIF4
title_full Guard cells control hypocotyl elongation through HXK1, HY5, and PIF4
title_fullStr Guard cells control hypocotyl elongation through HXK1, HY5, and PIF4
title_full_unstemmed Guard cells control hypocotyl elongation through HXK1, HY5, and PIF4
title_short Guard cells control hypocotyl elongation through HXK1, HY5, and PIF4
title_sort guard cells control hypocotyl elongation through hxk1, hy5, and pif4
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217561/
https://www.ncbi.nlm.nih.gov/pubmed/34155329
http://dx.doi.org/10.1038/s42003-021-02283-y
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