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

IF 10.6 Q1 HORTICULTURE Molecular Horticulture Pub Date : 2024-01-02 DOI:10.1186/s43897-023-00077-w
Pengwei Li, Yiling Zhang, Jing Liang, Xufan Hu, Yan He, Tonghao Miao, Zhiyin Ouyang, Zuchi Yang, Abdul Karim Amin, Chengcheng Ling, Yize Liu, Xiuhong Zhou, Xiaoran Lv, Runze Wang, Yajing Liu, Heqiang Huo, Yongsheng Liu, Wei Tang, Songhu Wang
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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.

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根瘤农杆菌介导的无标记转化和基因编辑系统发现,AeCBL3介导了猕猴桃草酸钙晶体的形成。
木本植物猕猴桃的基因转化和基因编辑既困难又耗时。针对猕猴桃的快速无标记基因修饰系统尚未开发出来。在此,我们建立了一个由根瘤农杆菌介导的快速、高效的猕猴桃无标记转化和基因编辑系统。此外,我们还开发了一种去除根尖的方法,以显著提高转基因毛根的再生效率。通过根瘤酵母介导的CRISPR/Cas9基因编辑,CEN4和AeCBL3的编辑效率分别达到55%和50%。并获得了这两个基因的多个同源基因敲除品系。我们的方法已成功应用于两个不同品种猕猴桃(Actinidia chinensis 'Hongyang' 和 A.eriantha 'White')的转化。接下来,我们用这种方法研究了猕猴桃中草酸钙(CaOx)晶体的形成。迄今为止,人们对草酸钙晶体在植物中的形成过程知之甚少。我们的研究结果表明,过表达 AeCBL3 会促进 CaOx 晶体的形成,但通过 CRISPR/Cas9 敲除 AeCBL3 会显著影响猕猴桃中晶体的形成。通过这些研究,我们开发出了一种用于猕猴桃的快速无制造者转化和高效 CRISPR-Cas9 基因编辑系统。此外,我们的工作还揭示了一种介导 CaOx 晶体形成的新基因,为阐明其潜在机制提供了线索。
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来源期刊
Molecular Horticulture
Molecular Horticulture horticultural research-
CiteScore
8.00
自引率
0.00%
发文量
24
审稿时长
12 weeks
期刊介绍: Aims Molecular Horticulture aims to publish research and review articles that significantly advance our knowledge in understanding how the horticultural crops or their parts operate mechanistically. Articles should have profound impacts not only in terms of high citation number or the like, but more importantly on the direction of the horticultural research field. Scope Molecular Horticulture publishes original Research Articles, Letters, and Reviews on novel discoveries on the following, but not limited to, aspects of horticultural plants (including medicinal plants): ▪ Developmental and evolutionary biology ▪ Physiology, biochemistry and cell biology ▪ Plant-microbe and plant-environment interactions ▪ Genetics and epigenetics ▪ Molecular breeding and biotechnology ▪ Secondary metabolism and synthetic biology ▪ Multi-omics dealing with data sets of genome, transcriptome, proteome, metabolome, epigenome and/or microbiome. The journal also welcomes research articles using model plants that reveal mechanisms and/or principles readily applicable to horticultural plants, translational research articles involving application of basic knowledge (including those of model plants) to the horticultural crops, novel Methods and Resources of broad interest. In addition, the journal publishes Editorial, News and View, and Commentary and Perspective on current, significant events and topics in global horticultural fields with international interests.
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