Interactions of cytosolic tails in the Jen1 carboxylate transporter are critical for trafficking and transport activity
Author(s) -
Cláudia Barata-Antunes,
Gabriel Talaia,
George Broutzakis,
David Manuel Nogueira Ribas,
Pieter De Beule,
Margarida Casal,
Christopher J. Stefan,
George Diallinas,
Sandra Paiva
Publication year - 2022
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.260059
Subject(s) - major facilitator superfamily , biology , endocytosis , transporter , microbiology and biotechnology , symporter , cytosol , transport protein , lactose permease , membrane transport protein , biogenesis , cytoplasm , function (biology) , biochemistry , cell , gene , enzyme
Plasma membrane (PM) transporters of the major facilitator superfamily (MFS) are essential for cell metabolism, growth and response to stress or drugs. In Saccharomyces cerevisiae, Jen1 is a monocarboxylate/H+ symporter that provides a model to dissect the molecular details underlying cellular expression, transport mechanism and turnover of MFS transporters. Here, we present evidence revealing novel roles of the cytosolic N- and C- termini of Jen1 in its biogenesis, PM stability and transport activity, using functional analyses of Jen1 truncations and chimeric constructs with UapA, an endocytosis-insensitive transporter of Aspergillus nidulans. Our results show that both N- and C-termini are critical for Jen1 trafficking to the PM, transport activity and endocytosis. Importantly, we provide evidence that Jen1 N- and C- termini undergo transport-dependent dynamic intra-molecular interactions, which affect the transport activity and turnover of Jen1. Our results support an emerging concept where the cytoplasmic termini of PM transporters control transporter cell-surface stability and function through flexible intra-molecular interactions with each other. These findings may be extended to other MFS members to understand conserved and evolving mechanisms underlying transporter structure-function relationships.
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