Involvement of the Membrane Nanodomain Protein, At Flot1, in Vesicular Transport of Plasma Membrane H + -ATPase in Arabidopsis thaliana under Salt Stress.

Autor: Khalilova, Lyudmila A., Lobreva, Olga V., Nedelyaeva, Olga I., Karpichev, Igor V., Balnokin, Yurii V.
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Zdroj: International Journal of Molecular Sciences; Jan2023, Vol. 24 Issue 2, p1251, 19p
Abstrakt: The aim of this study was to elucidate whether the membrane nanodomain protein AtFlot1 is involved in vesicular transport pathways and regulation of the P-type H+-ATPase content in plasma membrane of A. thaliana under salt stress. Transmission electron microscopy revealed changes in the endosomal system of A. thaliana root cells due to knockout mutation SALK_205125C (Atflot1ko). Immunoblotting of the plasma membrane-enriched fractions isolated from plant organs with an antibody to the H+-ATPase demonstrated changes in the H+-ATPase content in plasma membrane in response to the Atflot1ko mutation and salt shock. Expression levels of the main H+-ATPase isoforms, PMA1 and PMA2, as well as endocytosis activity of root cells determined by endocytic probe FM4-64 uptake assay, were unchanged in the Atflot1ko mutant. We have shown that AtFlot1 participates in regulation of the H+-ATPase content in the plasma membrane. We hypothesized that AtFlot1 is involved in both exocytosis and endocytosis, and, thus, contributes to the maintenance of cell ion homeostasis under salt stress. The lack of a pronounced Atflot1ko phenotype under salt stress conditions may be due to the assumed ability of Atflot1ko to switch vesicular transport to alternative pathways. Functional redundancy of AtFlot proteins may play a role in the functioning of these alternative pathways. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
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