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Vacuole integrity maintained by DUF300 proteins is required for brassinosteroid signaling regulation

  • Brassinosteroid (BR) hormone signaling controls multiple processes during plant growth and development and is initiated at the plasma membrane through the receptor kinase BRASSINOSTEROID INSENSITIVE1 (BRI1) together with co-receptors such as BRI1-ASSOCIATED RECEPTOR KINASE1 (BAK1). BRI1 abundance is regulated by endosomal recycling and vacuolar targeting, but the role of vacuole-related proteins in BR receptor dynamics and BR responses remains elusive. Here, we show that the absence of two DUF300 domain-containing tonoplast proteins, LAZARUS1 (LAZ1) and LAZ1 HOMOLOG1 (LAZ1H1), causes vacuole morphology defects, growth inhibition, and constitutive activation of BR signaling. Intriguingly, tonoplast accumulation of BAK1 was substantially increased and appeared causally linked to enhanced BRI1 trafficking and degradation in laz1 laz1h1 plants. Since unrelated vacuole mutants exhibited normal BR responses, our findings indicate that DUF300 proteins play distinct roles in the regulation of BR signaling by maintaining vacuole integrityBrassinosteroid (BR) hormone signaling controls multiple processes during plant growth and development and is initiated at the plasma membrane through the receptor kinase BRASSINOSTEROID INSENSITIVE1 (BRI1) together with co-receptors such as BRI1-ASSOCIATED RECEPTOR KINASE1 (BAK1). BRI1 abundance is regulated by endosomal recycling and vacuolar targeting, but the role of vacuole-related proteins in BR receptor dynamics and BR responses remains elusive. Here, we show that the absence of two DUF300 domain-containing tonoplast proteins, LAZARUS1 (LAZ1) and LAZ1 HOMOLOG1 (LAZ1H1), causes vacuole morphology defects, growth inhibition, and constitutive activation of BR signaling. Intriguingly, tonoplast accumulation of BAK1 was substantially increased and appeared causally linked to enhanced BRI1 trafficking and degradation in laz1 laz1h1 plants. Since unrelated vacuole mutants exhibited normal BR responses, our findings indicate that DUF300 proteins play distinct roles in the regulation of BR signaling by maintaining vacuole integrity required to balance subcellular BAK1 pools and BR receptor distribution.zeige mehrzeige weniger

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Metadaten
Verfasserangaben:Qinsong Liu, Thomas VainORCiD, Corrado ViottiORCiD, Siamsa M. Doyle, Danuse TarkowskaORCiD, Ondrej NovakORCiD, Cyril Zipfel, Folke Sitbon, Stephanie RobertORCiD, Daniel Hofius
DOI:https://doi.org/10.1016/j.molp.2017.12.015
ISSN:1674-2052
ISSN:1752-9867
Pubmed ID:https://pubmed.ncbi.nlm.nih.gov/29288738
Titel des übergeordneten Werks (Englisch):Molecular plant
Verlag:Cell Press
Verlagsort:Cambridge
Publikationstyp:Wissenschaftlicher Artikel
Sprache:Englisch
Datum der Erstveröffentlichung:27.12.2018
Erscheinungsjahr:2018
Datum der Freischaltung:13.12.2021
Freies Schlagwort / Tag:Arabidopsis; DUF300 proteins; brassinosteroid signaling; tonoplast; vacuole integrity
Band:11
Ausgabe:4
Seitenanzahl:15
Erste Seite:553
Letzte Seite:567
Fördernde Institution:Swedish University of Agricultural Sciences (SLU); Knut and Alice Wallenberg (KAW) FoundationKnut & Alice Wallenberg Foundation [2012-0087, 2012-0050]; Swedish Research Council (Vetenskapsradet, VR)Swedish Research Council [2016-04562, 2013-4632]; Vinnova (Verket for Innovationssystemet); Ministry of Education, Youth and Sports of the Czech Republic through the National Program of Sustainability [LO1204]
Organisationseinheiten:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
DDC-Klassifikation:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Peer Review:Referiert
Publikationsweg:Open Access / Bronze Open-Access
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