Identification of a Novel Amino Acid Response Pathway Triggering ATF2 Phosphorylation in Mammals

Author:

Chaveroux Cédric1,Jousse Céline1,Cherasse Yoan1,Maurin Anne-Catherine1,Parry Laurent1,Carraro Valérie1,Derijard Benoit2,Bruhat Alain1,Fafournoux Pierre1

Affiliation:

1. Unité de Nutrition Humaine, UMR 1019, INRA de Theix, 63122 Saint Genès Champanelle, France

2. Laboratoire de Physiologie Cellulaire et Moléculaire, CNRS UMR 6548, Faculté des Sciences, Université de Nice Sophia Antipolis, 28 Avenue Valrose, 06108 Nice Cedex 2, France

Abstract

ABSTRACT It has been well established that amino acid availability can control gene expression. Previous studies have shown that amino acid depletion induces transcription of the ATF3 (activation transcription factor 3) gene through an amino acid response element (AARE) located in its promoter. This event requires phosphorylation of activating transcription factor 2 (ATF2), a constitutive AARE-bound factor. To identify the signaling cascade leading to phosphorylation of ATF2 in response to amino acid starvation, we used an individual gene knockdown approach by small interfering RNA transfection. We identified the mitogen-activated protein kinase (MAPK) module MEKK1/MKK7/JNK2 as the pathway responsible for ATF2 phosphorylation on the threonine 69 (Thr69) and Thr71 residues. Then, we progressed backwards up the signal transduction pathway and showed that the GTPase Rac1/Cdc42 and the protein Gα12 control the MAPK module, ATF2 phosphorylation, and AARE-dependent transcription. Taken together, our data reveal a new signaling pathway activated by amino acid starvation leading to ATF2 phosphorylation and subsequently positively affecting the transcription of amino acid-regulated genes.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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