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高通量 CRISPR/Cas9 诱变技术简化了玉米性状基因的鉴定。

High-Throughput CRISPR/Cas9 Mutagenesis Streamlines Trait Gene Identification in Maize.

机构信息

National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan 430070, China.

National Key Laboratory of Crop Genetic Improvement, Huazhong Agricultural University, Wuhan 430070, China

出版信息

Plant Cell. 2020 May;32(5):1397-1413. doi: 10.1105/tpc.19.00934. Epub 2020 Feb 25.

DOI:10.1105/tpc.19.00934
PMID:32102844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7203946/
Abstract

Maize () is one of the most important crops in the world. However, few agronomically important maize genes have been cloned and used for trait improvement, due to its complex genome and genetic architecture. Here, we integrated multiplexed CRISPR/Cas9-based high-throughput targeted mutagenesis with genetic mapping and genomic approaches to successfully target 743 candidate genes corresponding to traits relevant for agronomy and nutrition. After low-cost barcode-based deep sequencing, 412 edited sequences covering 118 genes were precisely identified from individuals showing clear phenotypic changes. The profiles of the associated gene-editing events were similar to those identified in human cell lines and consequently are predictable using an existing algorithm originally designed for human studies. We observed unexpected but frequent homology-directed repair through endogenous templates that was likely caused by spatial contact between distinct chromosomes. Based on the characterization and interpretation of gene function from several examples, we demonstrate that the integration of forward and reverse genetics via a targeted mutagenesis library promises rapid validation of important agronomic genes for crops with complex genomes. Beyond specific findings, this study also guides further optimization of high-throughput CRISPR experiments in plants.

摘要

玉米是世界上最重要的作物之一。然而,由于其复杂的基因组和遗传结构,很少有农艺上重要的玉米基因被克隆并用于性状改良。在这里,我们将基于多重 CRISPR/Cas9 的高通量靶向诱变与遗传图谱和基因组方法相结合,成功地针对与农艺和营养相关的 743 个候选基因进行了靶向研究。在基于低成本条形码的深度测序后,从表现出明显表型变化的个体中,精确鉴定了 412 个覆盖 118 个基因的编辑序列。相关基因编辑事件的特征与在人类细胞系中鉴定的特征相似,因此可以使用最初为人类研究设计的现有算法进行预测。我们观察到了意想不到但频繁的同源定向修复,这可能是由不同染色体之间的空间接触引起的。基于对几个例子的基因功能的表征和解释,我们证明了通过靶向诱变文库将正向和反向遗传学相结合,有望快速验证具有复杂基因组的作物中重要的农艺基因。除了具体发现外,本研究还指导了植物中高通量 CRISPR 实验的进一步优化。

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本文引用的文献

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