Abstract

The eukaryotic translation elongation factor eEF-1Bβ1 (EF1Bβ) is a guanine nucleotide exchange factor that plays an important role in translation elongation. In this study, we show that the EF1Bβ protein is localized in the plasma membrane and cytoplasm, and that the transcripts should be expressed in most tissue types in seedlings. Sectioning of the inflorescence stem revealed that EF1Bβ predominantly localizes to the xylem vessels and in the interfascicular cambium. EF1Bβ gene silencing in efβ caused a dwarf phenotype with 38% and 20% reduction in total lignin and crystalline cellulose, respectively. This loss-of-function mutant also had a lower S/G lignin monomer ratio relative to wild type plants, but no changes were detected in a gain-of-function mutant transformed with the EF1Bβ gene. Histochemical analysis showed a reduced vascular apparatus, including smaller xylem vessels in the inflorescence stem of the loss-of-function mutant. Over-expression of EF1Bβ in an eli1 mutant background restored a WT phenotype and abolished ectopic lignin deposition as well as cell expansion defects in the mutant. Taken together, these data strongly suggest a role for EF1Bβ in plant development and cell wall formation in Arabidopsis.

Highlights

  • Translation is one of the vital processes involved in the fine regulation of gene expression through ensuring direct, rapid, reversible and spatial control of protein concentration [1], and thereby affects developmental processes in both prokaryotes and eukaryotes

  • Cytoskeleton and cell wall biosynthetic activities appear to be closely linked [11,12,37]. Due to this close relationship and the fact that EF1B is an actin-binding protein [13], we hypothesized that EF1Bb may play a role in plant development and cell wall biosynthesis

  • We found that EF1Bb is likely localized to the plasma membrane and cytosol

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Summary

Introduction

Translation is one of the vital processes involved in the fine regulation of gene expression through ensuring direct, rapid, reversible and spatial control of protein concentration [1], and thereby affects developmental processes in both prokaryotes and eukaryotes. Translation elongation in eukaryotes requires a set of soluble non-ribosomal proteins known as eukaryotic elongation factors or eEFs [2]. They include eEF1A and eEF1B factors, which are involved in the recruitment of aminoacyl-tRNAs onto the ribosome, and eEF2 factor, which mediates ribosomal translocation. The plant eEF1B is a trimer composed of the structural protein (eEF1Bc) plus two nucleotide exchange subunits (eEF1Ba and eEF1Bb) [6] and is intermediate in complexity between yeast and metazoans. The yeast eEF1B is made up of two subunits, a guanine nucleotide exchange protein (eEF1Ba) and a structural protein (eEF1Bc), whereas the metazoan complex is a heteromer of at least four subunits: the structural protein (eEF1Bc), two nucleotide exchange factors (eEF1Ba and eEF1Bd), plus the unique valine-tRNA synthetase (Val-RS) [6]. The nucleotide exchange function is achieved primarily by the eEF1Ba isoform, and the exact physiological functions of eEF1Bb and eEF1Bd are not yet known

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