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通过体内靶向 CRISPR/Cas9 活性加速抗性玉米自交系的下一代杂交技术。

Expediting Next-Generation Hybrid Technology in Recalcitrant Maize Inbreds through In Vivo Targeted Activity of CRISPR/Cas9.

机构信息

College of Agriculture, Yangtze University, Jingzhou 434000, China.

Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing 100081, China.

出版信息

Int J Mol Sci. 2024 May 27;25(11):5832. doi: 10.3390/ijms25115832.

Abstract

The Manipulated Genic Male Sterile Maintainer (MGM) system, a next-generation hybrid seed technology, enables efficient production of sortable seeds from genic male sterile (GMS) lines. However, implementing robust MGM systems in commercial maize inbred lines requires stable transformation, a genotype-specific and laborious process. This study aimed to integrate MGM technology into the commercial maize inbred line Z372, developing both GMS and MGM lines. We utilized the MGM line ZC01-3A-7, which contains the MS26ΔE5 editor T-DNA and MGM T-DNA, previously established in the highly transformable ZC01 recipient plants. Through a combination of crossing and backcrossing with Z372, we targeted the fertility gene within the Z372 genome for mutation using the in vivo CRISPR/Cas9 activity within the MS26ΔE5 editor T-DNA construct. This approach facilitated precise editing of the locus, minimizing linkage drag associated with the mutation. Whole-genome SNP analysis achieved a 98.74% recovery rate for GMS and 96.32% for MGM in the BC2F2 generation. Importantly, the Z372-GMS line with the mutation is non-transgenic, avoiding linkage drag and demonstrating production readiness. This study represents a significant advancement in maize breeding, enabling the rapid generation of GMS and MGM lines for efficient hybrid seed production.

摘要

转基因雄性不育保持系(MGM)系统是一种下一代杂交种子技术,能够从基因雄性不育(GMS)系中高效生产可分拣的种子。然而,在商业玉米自交系中实施稳健的 MGM 系统需要稳定的转化,这是一个特定于基因型且繁琐的过程。本研究旨在将 MGM 技术整合到商业玉米自交系 Z372 中,同时开发 GMS 和 MGM 系。我们利用了先前在高转化 ZC01 受体植物中建立的含有 MS26ΔE5 编辑 T-DNA 和 MGM T-DNA 的 MGM 系 ZC01-3A-7。通过与 Z372 的杂交和回交,我们利用 MS26ΔE5 编辑 T-DNA 构建体中的体内 CRISPR/Cas9 活性,针对 Z372 基因组中的育性基因进行突变。这种方法促进了 基因座的精确编辑,最大限度地减少了与 突变相关的连锁拖曳。在 BC2F2 代中,全基因组 SNP 分析实现了 GMS 的 98.74%恢复率和 MGM 的 96.32%恢复率。重要的是,具有 突变的 Z372-GMS 系是非转基因的,避免了连锁拖曳,并展示了生产准备就绪。这项研究代表了玉米育种的重大进展,能够快速生成 GMS 和 MGM 系,用于高效的杂交种子生产。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/568b/11172070/5db3bdaa4978/ijms-25-05832-g001.jpg

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