Interactions of cytosolic tails in the Jen1 carboxylate transporter are critical for trafficking and transport activity

Author:

Barata-Antunes Cláudia12ORCID,Talaia Gabriel13ORCID,Broutzakis George4ORCID,Ribas David1,De Beule Pieter5,Casal Margarida12,Stefan Christopher J.6ORCID,Diallinas George47ORCID,Paiva Sandra12ORCID

Affiliation:

1. Centre of Molecular and Environmental Biology, Department of Biology, University of Minho, 4710-057, Braga, Portugal

2. Institute of Science and Innovation for Bio-Sustainability (IB-S), University of Minho, 4710-057, Braga, Portugal

3. Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06510, USA

4. Department of Biology, National and Kapodistrian University of Athens, Panepistimiopolis 15784, Athens, Greece

5. International Iberian Nanotechnology Laboratory, Avenida Mestre José Veiga s/n, Braga, Portugal

6. MRC Laboratory for Molecular Cell Biology, University College London, Gower Street, London WC1E 6BT, UK

7. Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology, 70013, Heraklion, Greece

Abstract

ABSTRACT 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 intramolecular 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 intramolecular interactions with each other. These findings might be extended to other MFS members to understand conserved and evolving mechanisms underlying transporter structure–function relationships. This article has an associated First Person interview with the first authors of the paper.

Funder

Fundação para a Ciência e a Tecnologia

European Regional Development Fund

Fondation Sante

Publisher

The Company of Biologists

Subject

Cell Biology

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