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Lysophosphatidic acid acyltransferases: a link with intracellular protein trafficking in Arabidopsis root cells?
Author(s) -
Valérie WatteletBoyer,
Marina Le Guédard,
Franziska Dittrich-Domergue,
Lilly Maneta-Peyret,
Verena Kriechbaumer,
Yohann Boutté,
JeanJacques Bessoule,
Patrick Moreau
Publication year - 2021
Publication title -
journal of experimental botany
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.616
H-Index - 242
eISSN - 1460-2431
pISSN - 0022-0957
DOI - 10.1093/jxb/erab504
Subject(s) - lysophosphatidic acid , endomembrane system , phosphatidic acid , mutant , microbiology and biotechnology , arabidopsis thaliana , diacylglycerol kinase , biochemistry , arabidopsis , root hair , biology , acyltransferases , chemistry , golgi apparatus , enzyme , endoplasmic reticulum , protein kinase c , biosynthesis , membrane , phospholipid , receptor , gene
Phosphatidic acid (PA) and lysophosphatidic acid acyltransferases (LPAATs) might be critical for the secretory pathway. Four extra-plastidial LPAATs (LPAAT2, 3, 4, and 5) were identified in Arabidopsis thaliana. These AtLPAATs display a specific enzymatic activity converting lysophosphatidic acid to PA and are located in the endomembrane system. We investigate a putative role for AtLPAATs 3, 4, and 5 in the secretory pathway of root cells through genetical (knockout mutants), biochemical (activity inhibitor, lipid analyses), and imaging (live and immuno-confocal microscopy) approaches. Treating a lpaat4;lpaat5 double mutant with the LPAAT inhibitor CI976 produced a significant decrease in primary root growth. The trafficking of the auxin transporter PIN2 was disturbed in this lpaat4;lpaat5 double mutant treated with CI976, whereas trafficking of H+-ATPases was unaffected. The lpaat4;lpaat5 double mutant is sensitive to salt stress, and the trafficking of the aquaporin PIP2;7 to the plasma membrane in the lpaat4;lpaat5 double mutant treated with CI976 was reduced. We measured the amounts of neo-synthesized PA in roots, and found a decrease in PA only in the lpaat4;lpaat5 double mutant treated with CI976, suggesting that the protein trafficking impairment was due to a critical PA concentration threshold.

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