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High efficient multi-sites genome editing in allotetraploid cotton (Gossypium hirsutum) using CRISPR/Cas9 system

信息来源:作物遗传改良国家重点实验室    发布时间:2017-06-19
  • Pengcheng Wang,Jun Zhang,Lin Sun,Yizan Ma,Jiao Xu,Sijia Liang,Jinwu Deng, Jiafu Tan,Qinghua Zhang,Lili Tu, Henry Daniell, Shuangxia Jin, Xianlong Zhang

  • Plant Biotechnology Journal
  • Accepted manuscript online: 12 May 2017,DOI: 10.1111/pbi.12755

  • Abstract

    Gossypium hirsutum is an allotetraploid with a complex genome. Most genes have multiple copies that belong to At and Dt subgenomes. Sequence similarity is also very high between gene homologs. To efficiently achieve site/gene-specific mutation is quite needed. Due to its high efficiency and robustness, the CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas9 system has exerted broad site-specific genome editing from prokaryotes to eukaryotes. In this study, we utilized a CRISPR/Cas9 system to generate two sgRNAs in a single vector to conduct multiple sites genome editing in allotetraploid cotton. An exogenously transformed gene Discosoma red fluorescent protein2(DsRed2)and an endogenous gene GhCLA1 were chosen as targets. The DsRed2 edited plants in T0 generation reverted its traits to wild type, with vanished red fluorescence the whole plants. Besides, the mutated phenotype and genotype were inherited to their T1 progenies. For the endogenous gene GhCLA1, 75% of regenerated plants exhibited albino phenotype with obvious nucleotides and DNA fragments deletion. The efficiency of gene editing at each target site is 66.7% to 100% .The mutation genotype were checked for both genes with Sanger sequencing. Barcode-based high-throughput sequencing, which could be highly efficient for genotyping to a population of mutants, was conducted in GhCLA1 edited T0 plants and it matched well with Sanger sequencing results. No off-target editing was detected at the potential off-target sites. These results proves that the CRISPR/Cas9 system is highly efficient and reliable for allotetraploid cotton genome editing.

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