| Literature DB >> 28502081 |
Yunwei Zhang1,2, Yang Bai1,2, Guangheng Wu1,3, Shenghao Zou1, Yongfang Chen1, Caixia Gao1, Dingzhong Tang1,4,5.
Abstract
Wheat (Triticum aestivum L.) incurs significant yield losses from powdery mildew, a major fungal disease caused by Blumeria graminis f. sp. tritici (Bgt). enhanced disease resistance1 (EDR1) plays a negative role in the defense response against powdery mildew in Arabidopsis thaliana; however, the edr1 mutant does not show constitutively activated defense responses. This makes EDR1 an ideal target for approaches using new genome-editing tools to improve resistance to powdery mildew. We cloned TaEDR1 from hexaploid wheat and found high similarity among the three homoeologs of EDR1. Knock-down of TaEDR1 by virus-induced gene silencing or RNA interference enhanced resistance to powdery mildew, indicating that TaEDR1 negatively regulates powdery mildew resistance in wheat. We used CRISPR/Cas9 technology to generate Taedr1 wheat plants by simultaneous modification of the three homoeologs of wheat EDR1. No off-target mutations were detected in the Taedr1 mutant plants. The Taedr1 plants were resistant to powdery mildew and did not show mildew-induced cell death. Our study represents the successful generation of a potentially valuable trait using genome-editing technology in wheat and provides germplasm for disease resistance breeding.Entities:
Keywords: zzm321990Blumeria graminiszzm321990; CRISPR/Cas9; EDR1; Triticum aestivum L.; genome editing; hexaploid wheat; powdery mildew
Mesh:
Year: 2017 PMID: 28502081 DOI: 10.1111/tpj.13599
Source DB: PubMed Journal: Plant J ISSN: 0960-7412 Impact factor: 6.417