HPS4/SABRE regulates plant responses to phosphate starvation through antagonistic interaction with ethylene signalling

The phytohormone ethylene plays important roles in regulating plant responses to phosphate (Pi) starvation. To date, however, no molecular components have been identified that interact with ethylene signalling in regulating such responses. In this work, an Arabidopsis mutant, hps4, was characterized...

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Détails bibliographiques
Publié dans:Journal of experimental botany. - 1985. - 63(2012), 12 vom: 18. Juli, Seite 4527-38
Auteur principal: Yu, Hailan (Auteur)
Autres auteurs: Luo, Nan, Sun, Lichao, Liu, Dong
Format: Article en ligne
Langue:English
Publié: 2012
Accès à la collection:Journal of experimental botany
Sujets:Journal Article Research Support, Non-U.S. Gov't Anthocyanins Arabidopsis Proteins Ethylenes HPS4 protein, Arabidopsis Indoleacetic Acids Intracellular Signaling Peptides and Proteins Phosphates Plant Growth Regulators plus... indoleacetic acid 6U1S09C61L ethylene 91GW059KN7 Acid Phosphatase EC 3.1.3.2
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Résumé:The phytohormone ethylene plays important roles in regulating plant responses to phosphate (Pi) starvation. To date, however, no molecular components have been identified that interact with ethylene signalling in regulating such responses. In this work, an Arabidopsis mutant, hps4, was characterized that exhibits enhanced responses to Pi starvation, including increased inhibition of primary root growth, enhanced expression of Pi starvation-induced genes, and overproduction of root-associated acid phosphatases. Molecular cloning indicated that hps4 is a new allele of SABRE, which was previously identified as an important regulator of cell expansion in Arabidopsis. HPS4/SABRE antagonistically interacts with ethylene signalling to regulate plant responses to Pi starvation. Furthermore, it is shown that Pi-starved hps4 mutants accumulate more auxin in their root tips than the wild type, which may explain the increased inhibition of their primary root growth when grown under Pi deficiency
Description:Date Completed 17.04.2013
Date Revised 10.04.2022
published: Print-Electronic
Citation Status MEDLINE
ISSN:1460-2431
DOI:10.1093/jxb/ers131