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Unusual Roles of Secretory SNARE SYP132 in Plasma Membrane H+-ATPase Traffic and Vegetative Plant Growth
Author(s) -
Lingfeng Xia,
María Mar MarquèsBueno,
Craig Graham Bruce,
Rucha Karnik
Publication year - 2019
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.19.00266
Subject(s) - exocytosis , microbiology and biotechnology , endocytosis , apoplast , biology , atpase , arabidopsis , syntaxin , auxin , membrane , biochemistry , cell , cell wall , enzyme , gene , mutant
The plasma membrane proton (H + )-ATPases of plants generate steep electrochemical gradients and activate osmotic solute uptake. H + -ATPase-mediated proton pumping orchestrates cellular homeostasis and is a prerequisite for plastic cell expansion and plant growth. All evidence suggests that the population of H + -ATPase proteins at the plasma membrane reflects a balance of their roles in exocytosis, endocytosis, and recycling. Auxin governs both traffic and activation of the plasma membrane H + -ATPase proteins already present at the membrane. As in other eukaryotes, in plants, SNARE-mediated membrane traffic influences the density of several proteins at the plasma membrane. Even so, H + -ATPase traffic, its relationship with SNAREs, and its regulation by auxin have remained enigmatic. Here, we identify the Arabidopsis ( Arabidopsis thaliana ) Qa-SNARE SYP132 (Syntaxin of Plants132) as a key factor in H + -ATPase traffic and demonstrate its association with endocytosis. SYP132 is a low-abundant, secretory SNARE that primarily localizes to the plasma membrane. We find that SYP132 expression is tightly regulated by auxin and that augmented SYP132 expression reduces the amount of H + -ATPase proteins at the plasma membrane. The physiological consequences of SYP132 overexpression include reduced apoplast acidification and suppressed vegetative growth. Thus, SYP132 plays unexpected and vital roles in auxin-regulated H + -ATPase traffic and associated functions at the plasma membrane.

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