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Sugar signalling mediates cluster root formation and phosphorus starvation-induced gene expression in white lupin

Cluster root (CR) formation contributes much to the adaptation to phosphorus (P) deficiency. CR formation by white lupin (Lupinus albus L.) is affected by the P-limiting level in shoots, but not in roots. Thus, shoot-derived signals have been expected to transmit the message of P-deficiency to stimu...

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Autores principales: Zhou, Keqin, Yamagishi, Masumi, Osaki, Mitsuru, Masuda, Kiyoshi
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2486467/
https://www.ncbi.nlm.nih.gov/pubmed/18487637
http://dx.doi.org/10.1093/jxb/ern130
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author Zhou, Keqin
Yamagishi, Masumi
Osaki, Mitsuru
Masuda, Kiyoshi
author_facet Zhou, Keqin
Yamagishi, Masumi
Osaki, Mitsuru
Masuda, Kiyoshi
author_sort Zhou, Keqin
collection PubMed
description Cluster root (CR) formation contributes much to the adaptation to phosphorus (P) deficiency. CR formation by white lupin (Lupinus albus L.) is affected by the P-limiting level in shoots, but not in roots. Thus, shoot-derived signals have been expected to transmit the message of P-deficiency to stimulate CR formation. In this study, it is shown that sugars are required for a response to P starvation including CR formation and the expression of P starvation-induced genes. White lupin plants were grown in vitro on P-sufficient or P-deficient media supplemented with sucrose for 4 weeks. Sucrose supply stimulated CR formation in plants on both P-sufficient and P-deficient media, but no CR appeared on the P-sufficient medium without sucrose. Glucose and fructose also stimulated CR formation on the P-sufficient medium. On the medium with sucrose, a high concentration of inorganic phosphate in leaves did not suppress CR formation. Because sorbitol or organic acid in the media did not stimulate CR formation, the sucrose effect was not due to increased osmotic pressure or enriched energy source, that is, sucrose acted as a signal. Gene transcription induced by P starvation, LaPT1 and LaPEPC3, was magnified by the combination of P limitation and sucrose feeding, and that of LaSAP was stimulated by sucrose supply independently of P supply. These results suggest that at least two sugar-signalling mediating systems control P starvation responses in white lupin roots. One system regulates CR formation and LaSAP expression, which acts even when P is sufficient if roots receive sugar as a signal. The other system controls LaPT1 and LaPEPC3 expression, which acts when P is insufficient.
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spelling pubmed-24864672009-02-25 Sugar signalling mediates cluster root formation and phosphorus starvation-induced gene expression in white lupin Zhou, Keqin Yamagishi, Masumi Osaki, Mitsuru Masuda, Kiyoshi J Exp Bot Research Papers Cluster root (CR) formation contributes much to the adaptation to phosphorus (P) deficiency. CR formation by white lupin (Lupinus albus L.) is affected by the P-limiting level in shoots, but not in roots. Thus, shoot-derived signals have been expected to transmit the message of P-deficiency to stimulate CR formation. In this study, it is shown that sugars are required for a response to P starvation including CR formation and the expression of P starvation-induced genes. White lupin plants were grown in vitro on P-sufficient or P-deficient media supplemented with sucrose for 4 weeks. Sucrose supply stimulated CR formation in plants on both P-sufficient and P-deficient media, but no CR appeared on the P-sufficient medium without sucrose. Glucose and fructose also stimulated CR formation on the P-sufficient medium. On the medium with sucrose, a high concentration of inorganic phosphate in leaves did not suppress CR formation. Because sorbitol or organic acid in the media did not stimulate CR formation, the sucrose effect was not due to increased osmotic pressure or enriched energy source, that is, sucrose acted as a signal. Gene transcription induced by P starvation, LaPT1 and LaPEPC3, was magnified by the combination of P limitation and sucrose feeding, and that of LaSAP was stimulated by sucrose supply independently of P supply. These results suggest that at least two sugar-signalling mediating systems control P starvation responses in white lupin roots. One system regulates CR formation and LaSAP expression, which acts even when P is sufficient if roots receive sugar as a signal. The other system controls LaPT1 and LaPEPC3 expression, which acts when P is insufficient. Oxford University Press 2008-07 2008-05-17 /pmc/articles/PMC2486467/ /pubmed/18487637 http://dx.doi.org/10.1093/jxb/ern130 Text en © 2008 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. This paper is available online free of all access charges (see http://jxb.oxfordjournals.org/open_access.html for further details)
spellingShingle Research Papers
Zhou, Keqin
Yamagishi, Masumi
Osaki, Mitsuru
Masuda, Kiyoshi
Sugar signalling mediates cluster root formation and phosphorus starvation-induced gene expression in white lupin
title Sugar signalling mediates cluster root formation and phosphorus starvation-induced gene expression in white lupin
title_full Sugar signalling mediates cluster root formation and phosphorus starvation-induced gene expression in white lupin
title_fullStr Sugar signalling mediates cluster root formation and phosphorus starvation-induced gene expression in white lupin
title_full_unstemmed Sugar signalling mediates cluster root formation and phosphorus starvation-induced gene expression in white lupin
title_short Sugar signalling mediates cluster root formation and phosphorus starvation-induced gene expression in white lupin
title_sort sugar signalling mediates cluster root formation and phosphorus starvation-induced gene expression in white lupin
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2486467/
https://www.ncbi.nlm.nih.gov/pubmed/18487637
http://dx.doi.org/10.1093/jxb/ern130
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