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发根农杆菌介导的无标记转化和基因编辑系统表明,AeCBL3介导猕猴桃中草酸钙晶体的形成。

Agrobacterium rhizogenes-mediated marker-free transformation and gene editing system revealed that AeCBL3 mediates the formation of calcium oxalate crystal in kiwifruit.

作者信息

Li Pengwei, Zhang Yiling, Liang Jing, Hu Xufan, He Yan, Miao Tonghao, Ouyang Zhiyin, Yang Zuchi, Amin Abdul Karim, Ling Chengcheng, Liu Yize, Zhou Xiuhong, Lv Xiaoran, Wang Runze, Liu Yajing, Huo Heqiang, Liu Yongsheng, Tang Wei, Wang Songhu

机构信息

Anhui Provincial Key Laboratory of Horticultural Crop Quality Biology, School of Horticulture, Anhui Agricultural University, Hefei, 230036, China.

Mid-Florida Research and Education Center, University of Florida, Institute of Food and Agricultural Sciences, Apopka, FL, 32703, USA.

出版信息

Mol Hortic. 2024 Jan 2;4(1):1. doi: 10.1186/s43897-023-00077-w.

Abstract

The transformation and gene editing of the woody species kiwifruit are difficult and time-consuming. The fast and marker-free genetic modification system for kiwifruit has not been developed yet. Here, we establish a rapid and efficient marker-free transformation and gene editing system mediated by Agrobacterium rhizogenes for kiwifruit. Moreover, a removing-root-tip method was developed to significantly increase the regeneration efficiency of transgenic hairy roots. Through A. rhizogenes-mediated CRISPR/Cas9 gene editing, the editing efficiencies of CEN4 and AeCBL3 achieved 55 and 50%, respectively. And several homozygous knockout lines for both genes were obtained. Our method has been successfully applied in the transformation of two different species of kiwifruit (Actinidia chinensis 'Hongyang' and A.eriantha 'White'). Next, we used the method to study the formation of calcium oxalate (CaOx) crystals in kiwifruit. To date, little is known about how CaOx crystal is formed in plants. Our results indicated that AeCBL3 overexpression enhanced CaOx crystal formation, but its knockout via CRISPR/Cas9 significantly impaired crystal formation in kiwifruit. Together, we developed a fast maker-free transformation and highly efficient CRISPR-Cas9 gene editing system for kiwifruit. Moreover, our work revealed a novel gene mediating CaOx crystal formation and provided a clue to elaborate the underlying mechanisms.

摘要

木本植物猕猴桃的转化和基因编辑困难且耗时。目前尚未开发出用于猕猴桃的快速且无标记的遗传修饰系统。在此,我们建立了一种由发根农杆菌介导的快速高效的猕猴桃无标记转化和基因编辑系统。此外,还开发了一种去除根尖的方法,以显著提高转基因毛状根的再生效率。通过发根农杆菌介导的CRISPR/Cas9基因编辑,CEN4和AeCBL3的编辑效率分别达到了55%和50%。并且获得了这两个基因的多个纯合敲除株系。我们的方法已成功应用于两种不同猕猴桃品种(中华猕猴桃‘红阳’和毛花猕猴桃‘白’)的转化。接下来,我们使用该方法研究了猕猴桃中草酸钙(CaOx)晶体的形成。迄今为止,关于植物中草酸钙晶体如何形成知之甚少。我们的结果表明,AeCBL3的过表达增强了草酸钙晶体的形成,但通过CRISPR/Cas9对其进行敲除则显著损害了猕猴桃中晶体的形成。总之,我们为猕猴桃开发了一种快速的无标记转化和高效的CRISPR-Cas9基因编辑系统。此外,我们的工作揭示了一个介导草酸钙晶体形成的新基因,并为阐明其潜在机制提供了线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/087c/10759683/e0cec82c5658/43897_2023_77_Fig1_HTML.jpg

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