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CRISPR/Cas9介导的洋葱(L.)基因编辑。

CRISPR/Cas9-mediated editing of gene in onion ( L.).

作者信息

Mainkar Pawan, Manape Tushar Kashinath, Satheesh Viswanathan, Anandhan Sivalingam

机构信息

ICAR-Directorate of Onion and Garlic Research, Pune, Maharashtra, India.

Genome Informatics Facility, Office of Biotechnology, Iowa State University, Ames, IA, United States.

出版信息

Front Plant Sci. 2023 Aug 28;14:1226911. doi: 10.3389/fpls.2023.1226911. eCollection 2023.

Abstract

INTRODUCTION

Clustered regularly interspaced short palindromic repeats (CRISPR)/ CRISPR-associated protein 9 (Cas9) is a precise genome editing tool used to introduce genetic modifications in a wide range of crop species. Thus far, there is no report of CRISPR/Cas9-mediated genome editing in onions ().

METHODS

In the present study, we targeted two exons of the gene coding for Phytoene desaturase () in onion cv. Bhima Super. The sgRNA-carrying constructs were co-cultivated with 8-week-old embryogenic calli using an -mediated transformation protocol and incubated on the media without hygromycin B selection.

RESULTS AND DISCUSSION

Out of the total 617 co-cultivated calli, 21 (3.4%) regenerated shoots exhibited three distinct phenotypes: albino, chimeric, and pale green; in comparison to the wild-type non-transformed regenerated shoots. Total chlorophyll content was drastically reduced in albino shoots and significantly decreased in chimeric shoots. Out of the six gene PCR-confirmed regenerated shoots, two exhibited the albino phenotype due to insertions/deletions (InDels) and substitution-based mutations in and around the target sites. Deep amplicon sequencing revealed a significantly variable InDel frequency between two sgRNAs, ranging from 1.2% to 63.4%, along with a 53.4% substitution frequency. The mutation of the gene generated a visually detectable albino phenotype, thus confirming the successful editing of the gene. This is the first time a CRISPR/Cas9-mediated genome editing protocol has been successfully established in onion, with the gene serving as an example. This study will provide the necessary momentum for researchers to further basic and applied research on onions.

摘要

引言

成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关蛋白9(Cas9)是一种精确的基因组编辑工具,用于在多种作物物种中引入基因修饰。迄今为止,尚无关于CRISPR/Cas9介导的洋葱基因组编辑的报道。

方法

在本研究中,我们针对洋葱品种Bhima Super中编码八氢番茄红素去饱和酶()的基因的两个外显子。携带sgRNA的构建体使用-介导的转化方案与8周龄的胚性愈伤组织共培养,并在没有潮霉素B选择的培养基上培养。

结果与讨论

在总共617个共培养的愈伤组织中,21个(3.4%)再生芽表现出三种不同的表型:白化、嵌合和淡绿色;与野生型未转化的再生芽相比。白化芽中的总叶绿素含量急剧降低,嵌合芽中的总叶绿素含量显著降低。在六个经基因PCR确认的再生芽中,有两个由于目标位点及其周围的插入/缺失(InDels)和基于替换的突变而表现出白化表型。深度扩增子测序显示,两个sgRNA之间的InDel频率存在显著差异,范围从1.2%到63.4%,替换频率为53.4%。基因的突变产生了视觉上可检测到的白化表型,从而证实了基因的成功编辑。这是首次在洋葱中成功建立CRISPR/Cas9介导的基因组编辑方案,以基因为例。本研究将为研究人员进一步开展洋葱的基础研究和应用研究提供必要的动力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79bb/10494252/e71ad6e13a88/fpls-14-1226911-g001.jpg

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