State Key Laboratory of Cotton Biology/Institute of Cotton Research of Chinese Academy of Agricultural Sciences, Anyang, Henan 455000, China.
National Key Laboratory of Crop Genetic Improvement, College of Plant Sciences and Technology, Huazhong Agricultural University, Wuhan, Hubei 430070, China.
Sci Rep. 2017 Mar 13;7:44304. doi: 10.1038/srep44304.
The CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas9 system has been widely used for genome editing in various plants because of its simplicity, high efficiency and design flexibility. However, to our knowledge, there is no report on the application of CRISPR/Cas9-mediated targeted mutagenesis in cotton. Here, we report the genome editing and targeted mutagenesis in upland cotton (Gossypium hirsutum L., hereafter cotton) using the CRISPR/Cas9 system. We designed two guide RNAs to target distinct sites of the cotton Cloroplastos alterados 1 (GhCLA1) and vacuolar H-pyrophosphatase (GhVP) genes. Mutations in these two genes were detected in cotton protoplasts. Most of the mutations were nucleotide substitutions, with one nucleotide insertion and one substitution found in GhCLA1 and one deletion found in GhVP in cotton protoplasts. Subsequently, the two vectors were transformed into cotton shoot apexes through Agrobacterium-mediated transformation, resulting in efficient target gene editing. Most of the mutations were nucleotide deletions, and the mutation efficiencies were 47.6-81.8% in transgenic cotton plants. Evaluation using restriction-enzyme-PCR assay and sequence analysis detected no off-target mutations. Our results indicated that the CRISPR/Cas9 system was an efficient and specific tool for targeted mutagenesis of the cotton genome.
CRISPR(成簇规律间隔短回文重复)/Cas9 系统因其简单、高效和设计灵活性而被广泛应用于各种植物的基因组编辑。然而,据我们所知,CRISPR/Cas9 介导的靶向突变在棉花中的应用尚未见报道。在这里,我们报道了利用 CRISPR/Cas9 系统对陆地棉(Gossypium hirsutum L.,以下简称棉花)进行基因组编辑和靶向突变。我们设计了两个向导 RNA 来靶向棉花叶绿体改变 1(GhCLA1)和液泡 H-焦磷酸酶(GhVP)基因的不同位点。在棉花原生质体中检测到这两个基因的突变。这些突变大多是核苷酸取代,在 GhCLA1 中有一个核苷酸插入和一个取代,在 GhVP 中有一个缺失。随后,通过农杆菌介导的转化将这两个载体转化到棉花茎尖中,从而实现了高效的靶基因编辑。大多数突变是核苷酸缺失,在转基因棉花植株中的突变效率为 47.6-81.8%。利用酶切-PCR 检测和序列分析评估未检测到脱靶突变。我们的结果表明,CRISPR/Cas9 系统是一种针对棉花基因组进行靶向突变的有效和特异的工具。