Arabidopsis translation factor eEF1Bγ impacts plant development and is associated with heat-induced cytoplasmic foci

Author:

Lohmann Julia1,de Luxán-Hernández Cloe1,Gao Yang2ORCID,Zoschke Reimo2ORCID,Weingartner Magdalena1ORCID

Affiliation:

1. Institute of Plant Sciences and Microbiology, University of Hamburg, Ohnhorststrasse 18 , D-22609 Hamburg , Germany

2. Max Planck Institute of Molecular Plant Physiology , Am Mühlenberg 1, D-14476 Potsdam-Golm , Germany

Abstract

Abstract The important role of translational control for maintenance of proteostasis is well documented in plants, but the exact mechanisms that coordinate translation rates during plant development and stress response are not well understood. In Arabidopsis, the translation elongation complex eEF1B consists of three subunits: eEF1Bα, eEF1Bβ, and eEF1Bγ. While eEF1Bα and eEF1Bβ have a conserved GDP/GTP exchange function, the function of eEF1Bγ is still unknown. By generating Arabidopsis mutants with strongly reduced eEF1Bγ levels, we revealed its essential role during plant growth and development and analysed its impact on translation. To explore the function of the eEF1B subunits under high temperature stress, we analysed their dynamic localization as green fluorescent protein fusions under control and heat stress conditions. Each of these fusion proteins accumulated in heat-induced cytoplasmic foci and co-localized with the stress granule marker poly(A)-binding protein 8–mCherry. Protein–protein interaction studies and co-expression analyses indicated that eEF1Bβ physically interacted with both of the other subunits and promoted their recruitment to cytoplasmic foci. These data provide new insights into the mechanisms allowing for rapid adaptation of translation rates during heat stress response.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Physiology

Reference57 articles.

1. APUM23, a nucleolar Puf domain protein, is involved in pre-ribosomal RNA processing and normal growth patterning in Arabidopsis;Abbasi;The Plant Journal,2010

2. Approaches to investigating nuclear genes that function in chloroplast biogenesis in land plants.;Barkan,1998

3. Stem cell signaling in Arabidopsis requires CRN to localize CLV2 to the plasma membrane;Bleckmann;Plant Physiology,2010

4. Mechanism of cytoplasmic mRNA translation;Browning;The Arabidopsis Book,2015

5. Eukaryotic stress granules: the ins and outs of translation;Buchan;Molecular Cell,2009

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