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利用 CRISPR/Cas9 介导的 TMS5 编辑系统开发商用温敏基因雄性不育水稻加速杂交水稻育种。

Development of Commercial Thermo-sensitive Genic Male Sterile Rice Accelerates Hybrid Rice Breeding Using the CRISPR/Cas9-mediated TMS5 Editing System.

机构信息

State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangzhou 510642, China.

Key Laboratory of Plant Functional Genomics and Biotechnology of Guangdong Provincial Higher Education Institutions, Guangzhou 510642, China.

出版信息

Sci Rep. 2016 Nov 22;6:37395. doi: 10.1038/srep37395.

Abstract

Hybrid rice breeding offers an important strategy to improve rice production, in which the cultivation of a male sterile line is the key to the success of cross-breeding. CRISPR/Cas9 systems have been widely used in target-site genome editing, whereas their application for crop genetic improvement has been rarely reported. Here, using the CRISPR/Cas9 system, we induced specific mutations in TMS5, which is the most widely applied thermo-sensitive genic male sterility (TGMS) gene in China, and developed new "transgene clean" TGMS lines. We designed 10 target sites in the coding region of TMS5 for targeted mutagenesis using the CRISPR/Cas9 system and assessed the potential rates of on- and off-target effects. Finally, we established the most efficient construct, the TMS5ab construct, for breeding potentially applicable "transgene clean" TGMS lines. We also discussed factors that affect the editing efficiency according to the characteristics of different target sequences. Notably, using the TMS5ab construct, we developed 11 new "transgene clean" TGMS lines with potential applications in hybrid breeding within only one year in both rice subspecies. The application of our system not only significantly accelerates the breeding of sterile lines but also facilitates the exploitation of heterosis.

摘要

杂交水稻育种提供了提高水稻产量的重要策略,其中培育雄性不育系是杂交成功的关键。CRISPR/Cas9 系统已广泛应用于靶标基因组编辑,但其在作物遗传改良中的应用鲜有报道。在这里,我们使用 CRISPR/Cas9 系统在 TMS5 中诱导特定突变,TMS5 是中国应用最广泛的温敏基因雄性不育(TGMS)基因,并开发了新的“转基因清洁”TGMS 系。我们在 TMS5 的编码区设计了 10 个靶标位点,用于使用 CRISPR/Cas9 系统进行靶向诱变,并评估潜在的脱靶效应和脱靶效应率。最后,我们建立了最有效的构建体 TMS5ab 用于培育潜在适用的“转基因清洁”TGMS 系。我们还根据不同靶序列的特点讨论了影响编辑效率的因素。值得注意的是,使用 TMS5ab 构建体,我们仅在一年内在两个水稻亚种中开发了 11 种新的“转基因清洁”TGMS 系,具有潜在的杂交育种应用价值。我们的系统的应用不仅显著加快了不育系的培育速度,而且还促进了杂种优势的利用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8379/5118805/dfbd37e72bce/srep37395-f1.jpg

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