Abstract

The APETALA 2/Ethylene-responsive element binding factor (AP2/ERF) transcription factor gene family is widely involved in the biotic and abiotic stress regulation. Haynaldia villosa (VV, 2n = 14), a wild species of wheat, is a potential gene pool for wheat improvement. H. villosa confers high resistance to several wheat diseases and high tolerance to some abiotic stress. In this study, ERF1-V, an ethylene-responsive element-binding factor gene of the AP2/ERF transcription factor gene family from wild H. villosa, was cloned and characterized. Sequence and phylogenetic analysis showed that ERF1-V is a deduced B2 type ERF gene. ERF1-V was first identified as a Blumeria graminis f. sp. tritici (Bgt) up-regulated gene, and later found to be induced by drought, salt and cold stresses. In responses to hormones, ERF1-V was up-regulated by ethylene and abscisic acid, but down-regulated by salicylic acid and jasmonic acid. Over expression of ERF1-V in wheat could improve resistance to powdery mildew, salt and drought stress. Chlorophyll content, malondialdehyde content, superoxide dismutase and peroxidase activity were significantly differences between the recipient Yangmai158 and the transgenic plants following salt treatment. Furthermore, the expression levels of some stress responsive genes were differences after drought or salt treatments. Although ERF1-V was activated by the constitutive promoter, the agronomic traits, including flowering time, plant height, effective tiller number, spikelet number per spike and grain size, did not changed significantly. ERF1-V is a valuable gene for wheat improvement by genetic engineering.

Highlights

  • Transcription factors (TFs) have been shown to control the activation of multiple stress response genes (Meshi and Iwabuchi, 1995)

  • The aim of this study was to identify whether the ERF1-V gene of the APETALA 2/Ethylene-responsive element binding factor (AP2/ERF) family is involved in powdery mildew resistance and salt and drought stress tolerance of wheat

  • To identify the resistance related genes and to study the resistance mechanism, the transcription profiles of H. villosa were obtained by GeneChip microarray, and the data were compared between the Blumeria graminis f. sp. tritici (Bgt) inoculated sample and the uninoculated sample

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Summary

Introduction

Transcription factors (TFs) have been shown to control the activation of multiple stress response genes (Meshi and Iwabuchi, 1995). APETALA 2/Ethylene-responsive element binding factor (AP2/ERF), the largest family of TFs in plants, is characterized by a highly conserved AP2/ethylene-responsive element-binding factor DNA-binding domain (BD). ERF1-V Enhanced Multiple Stress Tolerance (Riechmann and Meyerowitz, 1998). This TF family has been identified in plants such as APETALA2 of Arabidopsis (Jofuku et al, 1994) and EREBP1 of tobacco (Ohme-Takagi and Shinshi, 1995). The AP2/ERF genes are divided into five subfamilies, including APETALA2 factor (AP2), Dehydration responsive element binding factor (DREB), Ethylene responsive element binding factor (ERF), Related to ABI3/VP (RAV) and Soloist subfamilies, based on the number and similarity of their AP2/ERFBP domains (Li et al, 2013)

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