Journal of Integrative Agriculture ›› 2026, Vol. 25 ›› Issue (5): 1836-1845.DOI: 10.1016/j.jia.2024.09.011

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利用内源pGhαGloA启动子介导的CRISPR/Cas12a系统进行高效基因组编辑并创造无腺体棉花种质

  

  • 收稿日期:2024-04-24 修回日期:2024-09-21 接受日期:2024-07-10 出版日期:2026-05-20 发布日期:2026-04-09

Application of an endogenous pGhαGloA promoter in the CRISPR/Cas12a system for efficient genome editing to create glandless cotton germplasm

Chenyu Li1, 3*, Zumuremu Tuerxun1*, Yang Yang1, Xiaorong Li1, Fengjiao Hui2, Juan Li1 , Zhigang Liu1, Guo Chen1, Darun Cai1, Hui Zhang1, Xunji Chen1, Shuangxia Jin2#, Bo Li1#   

  1. 1 Xinjiang Key Laboratory of Crop Biotechnology/Biological Breeding Laboratory, Xinjiang Uygur Autonomous Region Academy of Agricultural Sciences, Urumqi 830091, China

    2 Hubei Hongshan Laboratory/National Key Laboratory of Crop Genetic Improvement/Huazhong Agricultural University, Wuhan 430070, China

    3 College of Agronomy, Xinjiang Agricultural University, Urumqi 830052, China

  • Received:2024-04-24 Revised:2024-09-21 Accepted:2024-07-10 Online:2026-05-20 Published:2026-04-09
  • About author:#Correspondence Shuangxia Jin, E-mail: jsx@mail.hzau.edu.cn; Bo Li, E-mail: lbharrywei@sina.com * These authors contributed equally to this study.
  • Supported by:

    This study was financially supported by Major Science and Technology Project of Xinjiang Uygur Autonomous Region, China (2023A02003-2) to Bo Li, STI 2030-Major Projects (2023ZD04074) to Dr. Shuangxia Jin, Tianshan Talent training program of Xinjiang Uygur Autonomous Region, China (2023TSYCJU0001), the earmarked fund for XinJiang Agriculture Research System, China (XJARS-3) and the Project of Fund for Stable Support to Agricultural Sci-Tech Renovation (xjnkywdzc-2022001-1) to Bo Li.

摘要:

CRISPR/Cas 12a系统是一种高效的基因组编辑工具,在植物功能基因组学研究和农艺性状改良中得到了广泛应用。本研究利用棉花内源pGhαGloA启动子对CRISPR/Cas 12a系统进行了优化。利用该系统,在Pol II类型的pGhaGloA启动子的驱动下,构建了pGhRBE3-pGhαGloA-GhPGF载体,并进行了遗传转化。该载体在所有阳性转基因植株中均能有效工作,crRNA1靶位点的编辑效率高达93.37%crRNA2靶位点的编辑效率高达88.24%明显高于Pol III启动子-Ubi 6.7驱动的pGhRBE3系统的编辑效率,表明Pol II启动子比Pol III启动子更适合于在棉花中表达多种sgRNAcrRNA。该载体主要编辑类型呈现片段缺失,缺失片段大小在3-12 bp之间,编辑位点位于PAM下游第14 ~ 29位碱基。这些突变位点在T0T2代均能稳定遗传,同时获得了3GhPGF基因突变的DNA-Free系,这些无棉酚或低酚棉花种质将对棉籽油/的健康生产起重要用。因此,pGhαGloA启动子驱动的CRISPR/Cas 12a系统可以在棉花中高效编辑靶标基因,为棉花功能基因组学和遗传改良提供了有力的工具。

Abstract:

An efficient genome editing tool, the CRISPR/Cas12a system, has been used in research on plant functional genomics and the improvement of agronomic traits.  In this study, the CRISPR/Cas12a system was optimized by using the endogenous pGhαGloA promoter in cotton.  With this system, crRNAs were driven by the Pol II pGhaGloA promoter to construct the pGhRBE3-pGhαGloA-GhPGF vector and carry out genetic transformation.  The vector worked efficiently in all positive transgenic plants and the editing efficiencies at the crRNA1 and crRNA2 target sites were up to 93.37 and 88.24%, respectively.  This system had significantly higher editing efficiency than the pGhRBE3 system with a Pol III promoter-Ubi 6.7 promoter, indicating that the Pol II promoter is more suitable for expressing multiple sgRNAs or crRNAs than the Pol III promoter in cotton.  The vector mainly generated the editing type of fragment deletion, and the deletion sizes were in the range of 3–12 bp with the editing sites spanning the 14th to 29th bases downstream of the protospacer adjacent motif (PAM).  All the targeted mutation loci were stably inherited from the T0 to T2 generations, and three transgene-free lines with target site mutations in the GhPGF gene were obtained.  These glandless and gossypol-free (or low content) cotton germplasms will play a key role in healthy cottonseed oil/cake production.  Therefore, the CRISPR/Cas12a system driven by the pGhαGloA promoter can efficiently edit target genes in cotton, so it can provide a powerful tool for cotton functional genomics and genetic improvement.

Key words: cotton , genome editing ,  CRISPR/Cas12a ,  Pol II promoter ,  glandless cotton ,  gossypol-free