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通过Cas12a/CBE共编辑在T0代产生无转基因的抗溃疡病哈姆林甜橙品种。

Generation of transgene-free canker-resistant cv. Hamlin in the T0 generation through Cas12a/CBE co-editing.

作者信息

Jia Hongge, Omar Ahmad A, Xu Jin, Dalmendray Javier, Wang Yuanchun, Feng Yu, Wang Wenting, Hu Zhuyuan, Grosser Jude W, Wang Nian

机构信息

Citrus Research and Education Center, Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences (IFAS), University of Florida, Lake Alfred, FL, United States.

Citrus Research and Education Center, Horticultural Sciences Department, Institute of Food and Agricultural Sciences (IFAS), University of Florida, Lake Alfred, FL, United States.

出版信息

Front Plant Sci. 2024 Mar 26;15:1385768. doi: 10.3389/fpls.2024.1385768. eCollection 2024.

Abstract

Citrus canker disease affects citrus production. This disease is caused by subsp. citri (Xcc). Previous studies confirmed that during Xcc infection, PthA4, a transcriptional activator like effector (TALE), is translocated from the pathogen to host plant cells. PthA4 binds to the effector binding elements (EBEs) in the promoter region of canker susceptibility gene (EBE-LOBP) to activate its expression and subsequently cause canker symptoms. Previously, the Cas12a/CBE co-editing method was employed to disrupt EBE-LOBP of pummelo, which is highly homozygous. However, most commercial citrus cultivars are heterozygous hybrids and more difficult to generate homozygous/biallelic mutants. Here, we employed Cas12a/CBE co-editing method to edit EBE-LOBP of Hamlin (), a commercial heterozygous hybrid citrus cultivar grown worldwide. Binary vector GFP-p1380N-ttLbCas12a:LOBP1-mPBE:ALS2:ALS1 was constructed and shown to be functional via Xcc-facilitated agroinfiltration in Hamlin leaves. This construct allows the selection of transgene-free regenerants via GFP, edits to generate chlorsulfuron-resistant regenerants as a selection marker for genome editing resulting from transient expression of the T-DNA via nCas9-mPBE:ALS2:ALS1, and edits gene(s) of interest (i.e., EBE-LOBP in this study) through ttLbCas12a, thus creating transgene-free citrus. Totally, 77 plantlets were produced. Among them, 8 plantlets were transgenic plants (#Ham1 - #Ham8), 4 plantlets were transgene-free (#Ham1 - #Ham4), and the rest were wild type. Among 4 transgene-free plantlets, three lines (#Ham1, #Ham2 and #Ham3) contained biallelic mutations in EBE, and one line (#Ham4) had homozygous mutations in EBE. We achieved 5.2% transgene-free homozygous/biallelic mutation efficiency for EBE-LOBP in cv. Hamlin, compared to 1.9% mutation efficiency for pummelo in a previous study. Importantly, the four transgene-free plantlets and 3 transgenic plantlets that survived were resistant against citrus canker. Taken together, Cas12a/CBE co-editing method has been successfully used to generate transgene-free canker-resistant cv. Hamlin in the T0 generation via biallelic/homozygous editing of EBE of the canker susceptibility gene

摘要

柑橘溃疡病影响柑橘生产。这种病害由柑橘溃疡病菌(Xcc)引起。先前的研究证实,在Xcc感染期间,一种类转录激活因子效应子(TALE)PthA4从病原菌转移至宿主植物细胞。PthA4与溃疡病易感基因(EBE - LOBP)启动子区域的效应子结合元件(EBEs)结合,以激活其表达,进而引发溃疡病症状。此前,采用Cas12a/CBE共编辑方法破坏了高度纯合的柚的EBE - LOBP。然而,大多数商业化柑橘品种是杂合杂种,更难产生纯合/双等位基因突变体。在此,我们采用Cas12a/CBE共编辑方法编辑哈姆林甜橙(Hamlin)的EBE - LOBP,哈姆林甜橙是一种在全球种植的商业化杂合柑橘品种。构建了二元载体GFP - p1380N - ttLbCas12a:LOBP1 - mPBE:ALS2:ALS1,并通过Xcc促进的农杆菌浸润在哈姆林甜橙叶片中证明其具有功能。该构建体允许通过GFP选择无转基因再生植株,通过nCas9 - mPBE:ALS2:ALS1瞬时表达T - DNA进行编辑以产生抗氯磺隆的再生植株作为基因组编辑的选择标记,并通过ttLbCas12a编辑目标基因(即本研究中的EBE - LOBP),从而培育出无转基因柑橘。总共产生了77株幼苗。其中,8株幼苗为转基因植株(#Ham1 - #Ham8),4株幼苗为无转基因植株(#Ham1 - #Ham4),其余为野生型。在4株无转基因幼苗中,3个株系(#Ham1、#Ham2和#Ham3)的EBE中存在双等位基因突变,1个株系(#Ham4)的EBE中存在纯合突变。我们在哈姆林甜橙品种中实现了EBE - LOBP的无转基因纯合/双等位基因突变效率为5.2%,而先前研究中柚的突变效率为1.9%。重要的是,存活下来的4株无转基因幼苗和3株转基因幼苗对柑橘溃疡病具有抗性。综上所述,Cas12a/CBE共编辑方法已成功用于通过对溃疡病易感基因的EBE进行双等位基因/纯合编辑,在T0代培育出无转基因的抗溃疡病哈姆林甜橙品种

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccd9/11002166/151e50579fe4/fpls-15-1385768-g001.jpg

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