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LPCAT1 controls phosphate homeostasis in a zinc-dependent manner

All living organisms require a variety of essential elements for their basic biological functions. While the homeostasis of nutrients is highly intertwined, the molecular and genetic mechanisms of these dependencies remain poorly understood. Here, we report a discovery of a molecular pathway that co...

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Autores principales: Kisko, Mushtak, Bouain, Nadia, Safi, Alaeddine, Medici, Anna, Akkers, Robert C, Secco, David, Fouret, Gilles, Krouk, Gabriel, Aarts, Mark GM, Busch, Wolfgang, Rouached, Hatem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5826268/
https://www.ncbi.nlm.nih.gov/pubmed/29453864
http://dx.doi.org/10.7554/eLife.32077
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author Kisko, Mushtak
Bouain, Nadia
Safi, Alaeddine
Medici, Anna
Akkers, Robert C
Secco, David
Fouret, Gilles
Krouk, Gabriel
Aarts, Mark GM
Busch, Wolfgang
Rouached, Hatem
author_facet Kisko, Mushtak
Bouain, Nadia
Safi, Alaeddine
Medici, Anna
Akkers, Robert C
Secco, David
Fouret, Gilles
Krouk, Gabriel
Aarts, Mark GM
Busch, Wolfgang
Rouached, Hatem
author_sort Kisko, Mushtak
collection PubMed
description All living organisms require a variety of essential elements for their basic biological functions. While the homeostasis of nutrients is highly intertwined, the molecular and genetic mechanisms of these dependencies remain poorly understood. Here, we report a discovery of a molecular pathway that controls phosphate (Pi) accumulation in plants under Zn deficiency. Using genome-wide association studies, we first identified allelic variation of the Lyso-PhosphatidylCholine (PC) AcylTransferase 1 (LPCAT1) gene as the key determinant of shoot Pi accumulation under Zn deficiency. We then show that regulatory variation at the LPCAT1 locus contributes significantly to this natural variation and we further demonstrate that the regulation of LPCAT1 expression involves bZIP23 TF, for which we identified a new binding site sequence. Finally, we show that in Zn deficient conditions loss of function of LPCAT1 increases the phospholipid Lyso-PhosphatidylCholine/PhosphatidylCholine ratio, the expression of the Pi transporter PHT1;1, and that this leads to shoot Pi accumulation.
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spelling pubmed-58262682018-02-28 LPCAT1 controls phosphate homeostasis in a zinc-dependent manner Kisko, Mushtak Bouain, Nadia Safi, Alaeddine Medici, Anna Akkers, Robert C Secco, David Fouret, Gilles Krouk, Gabriel Aarts, Mark GM Busch, Wolfgang Rouached, Hatem eLife Plant Biology All living organisms require a variety of essential elements for their basic biological functions. While the homeostasis of nutrients is highly intertwined, the molecular and genetic mechanisms of these dependencies remain poorly understood. Here, we report a discovery of a molecular pathway that controls phosphate (Pi) accumulation in plants under Zn deficiency. Using genome-wide association studies, we first identified allelic variation of the Lyso-PhosphatidylCholine (PC) AcylTransferase 1 (LPCAT1) gene as the key determinant of shoot Pi accumulation under Zn deficiency. We then show that regulatory variation at the LPCAT1 locus contributes significantly to this natural variation and we further demonstrate that the regulation of LPCAT1 expression involves bZIP23 TF, for which we identified a new binding site sequence. Finally, we show that in Zn deficient conditions loss of function of LPCAT1 increases the phospholipid Lyso-PhosphatidylCholine/PhosphatidylCholine ratio, the expression of the Pi transporter PHT1;1, and that this leads to shoot Pi accumulation. eLife Sciences Publications, Ltd 2018-02-17 /pmc/articles/PMC5826268/ /pubmed/29453864 http://dx.doi.org/10.7554/eLife.32077 Text en © 2018, Kisko et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Plant Biology
Kisko, Mushtak
Bouain, Nadia
Safi, Alaeddine
Medici, Anna
Akkers, Robert C
Secco, David
Fouret, Gilles
Krouk, Gabriel
Aarts, Mark GM
Busch, Wolfgang
Rouached, Hatem
LPCAT1 controls phosphate homeostasis in a zinc-dependent manner
title LPCAT1 controls phosphate homeostasis in a zinc-dependent manner
title_full LPCAT1 controls phosphate homeostasis in a zinc-dependent manner
title_fullStr LPCAT1 controls phosphate homeostasis in a zinc-dependent manner
title_full_unstemmed LPCAT1 controls phosphate homeostasis in a zinc-dependent manner
title_short LPCAT1 controls phosphate homeostasis in a zinc-dependent manner
title_sort lpcat1 controls phosphate homeostasis in a zinc-dependent manner
topic Plant Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5826268/
https://www.ncbi.nlm.nih.gov/pubmed/29453864
http://dx.doi.org/10.7554/eLife.32077
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