CRISPR/Cas9系统介导的棉花GhNAC3基因编辑
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1.新疆农垦科学院生物技术研究所/作物种质创新与基因资源利用兵团重点实验室;2.新疆生产建设兵团第一师农业科学研究所

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S562????

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新疆农垦科学院院级项目(03110004);八师石河子市中青年科技创新骨干人才计划(2022RC03);第一师阿拉尔市科技计划项目(2022NY10);新疆农垦科学院创新团队


CRISPR/Cas9 Targeted Editing of GhNAC3 in Cotton
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    摘要:

    棉花是世界上最重要的纤维作物和重要的油料作物。新疆是我国最大的棉花产区,然而,干旱胁迫已成为影响棉花生产的主要非生物逆境因素。挖掘耐旱的关键调控因子并加以利用,进而培育耐旱性棉花品种,是解决棉花耐旱资源贫乏及提高水资源利用率的有效途径。本研究依据 CRISPR/Cas9 编辑原理,对课题组前期利用RT-PCR技术筛选耐旱相关基因GhNAC3(Gh_D02G0790)第 1 外显子区域设计 2 个 20 bp 的编辑靶点,并在陆地棉基因组数据库中比对分析靶点序列,排除非特异性编辑,将 2 个靶点核苷酸片段分别与gRNA-atU6载体连接,通过 2 次 PCR 扩增,得到含特异性连接接头的 atU6-GhNAC3 表达盒,再将表达盒连接到 CRISPR/Cas9(pRGEB32-7)载体上,获得CRISPR-GhNAC3 重组表达载体,利用农杆菌介导法转化陆地棉受体 YZ-1 ,再生培养得到 T0代转基因幼苗,通过 PCR 检测 Cas9 蛋白基因获得阳性株系。对 T0 代植株的靶点区域序列进行 PCR 扩增和测序分析,鉴定GhNAC3 编辑类型。结果发现,CRISPR9-GhNAC3 表达载体成功转化 YZ-1 ,并获得 40 株转基因再生植株,经 Cas9 蛋白基因鉴定得到 30 株阳性株系,从阳性植株选择 10 株进行编辑类型测序分析,发现 7 株在靶点区域都发生编辑,编辑类型主要为碱基片段缺失,缺失片段大小为 3-28bp,T1代种植于大田,获得了同时出现黄化和矮化的突变体 3 株。结果表明,采用 CRISPR/Cas9 技术对 GhNAC3 序列进行编辑,获得了表型变异的突变体,充分说明该基因参与了棉花生长发育的调控。

    Abstract:

    Cotton is one of the most important economic crops in the world, as well as the most important fiber crop and important oil crop. Xinjiang is the largest region of cotton producing in China. However, cotton production has affected by drought stress become the main abiotic stress factor . It is an effective way to address the scarcity of cotton drought resistance resources and improve water resource utilization is exploiting and utilizing key regulatory factors for drought resistance and cultivating drought resistant cotton varieties. According to the principle of CRISPR/Cas9 technology, two 20 bp targeted sequences were designed in the first exon of the GhNAC3 genome sequence. The gene shuffling of non-specific target sites was eliminated using the blast analysis. The oligonucleotides of two target sites were inserted into the gRNA-atU6 plasmid vector, and then were amplified twice by PCR technology to construct atU6-GhNAC3 expression-boxes. The recombinant CRISPR-GhNAC3 vector was obtained by linking two expression-boxes to CRISPR/Cas9(pRGEB32-7) vector. The CRISPR-GhNAC3 vector was transformed into the cotton of YZ-1 through agrobacterium mediated method. The T0 generation of transgenic plants was obtained by detection of Cas9 protein gene , and the positive transgenic plants were selected through PCR method. The target sites of each T0 generation from were determined [收稿日期: 基金项目:新疆农垦科学院院级项目(03110004);八师石河子市中青年科技创新骨干人才计划(2022RC03);第一师阿拉尔市科技计划项目(2022NY10);新疆农垦科学院创新团队 作者简介:王志军(1985-),博士,助理研究员,作物遗传育种,E-mail:wzjshihezi@163.com *通信作者:马盼盼,副研究员,研究方向,作物抗逆种质创新及育种,E-mail:mp20044681@163.com]via PCR and sequencing method, and finally the mutated genotypes were identified. After Cas9 protein gene identification, 30 positive strains were obtained, and 10 of them were selected from the positive plants for editing type sequencing analysis. It was found that all 7 strains underwent editing in the target region. The editing type was mainly base fragment deletion, with a deletion fragment size of 3-28 bp. T1 was planted in the field, and 3 mutants with both yellowing and dwarfing were obtained. The results showed that using CRISPR/Cas9 technology to edit the GhNAC3 sequence, plants with phenotypic variations were obtained, fully demonstrating that the gene is involved in the regulation of cotton growth and development.

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王志军,何宗铃,张国丽,等. CRISPR/Cas9系统介导的棉花GhNAC3基因编辑[J].西北植物学报,2023,43(11):1834-1841

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  • 收稿日期:2023-04-13
  • 最后修改日期:2023-08-13
  • 录用日期:2023-09-01
  • 在线发布日期: 2023-11-14
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