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Genome Editing of Rice Loci Confers Partial Resistance to Rice Black-Streaked Dwarf Virus

Viruses. 2021-10; 
Wei Wang, Shuhui Ma, Peng Hu, Yinghua Ji, Feng Sun
Products/Services Used Details Operation
PCR Cloning and Subcloning … These sgRNA oligos were synthesized (Genscript, Nanjing, China) and cloned into the pHUE401 vector by Golden Gate cloning, as previously described [26]. CRISPR/Cas9 vectors were introduced into Agrobacterium tumefaciens strain GV3101 by electroporation and … Get A Quote

Abstract

Rice black-streaked dwarf disease, caused by rice black-streaked dwarf virus (RBSDV), is a serious constraint in Chinese rice production. Breeding disease-resistant varieties through multigene aggregation is considered an effective way to control diseases, but few disease-resistant resources have been characterized thus far. To develop novel resources for resistance to RBSDV through CRISPR/Cas9-mediated genome editing, a guide RNA sequence targeting exon 1 of was designed and cloned into a binary vector, pHUE401. This recombinant vector was used to generate mutations in the rice cultivar Nipponbare via -mediated transformation. This approach produced heritable homozygous mutations in the transgene-free T1 gene... More

Keywords

CRISPR/Cas9, RBSDV, eIF4G, genome editing, virus resistance