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利用CRISPR-Cas9系统对异源四倍体油菜中溶血磷脂酸酰基转移酶2/5进行有效编辑。

Effective editing for lysophosphatidic acid acyltransferase 2/5 in allotetraploid rapeseed ( L.) using CRISPR-Cas9 system.

作者信息

Zhang Kai, Nie Liluo, Cheng Qiqi, Yin Yongtai, Chen Kang, Qi Fuyu, Zou Dashan, Liu Haohao, Zhao Weiguo, Wang Baoshan, Li Maoteng

机构信息

1Department of Biotechnology, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, China.

2Hubei Key Laboratory of Economic Forest Germplasm Improvement and Resources Comprehensive Utilization, Hubei Collaborative Innovation Center for the Characteristic Resources Exploitation of Dabie Mountains, Huanggang Normal University, Huanggang, China.

出版信息

Biotechnol Biofuels. 2019 Sep 20;12:225. doi: 10.1186/s13068-019-1567-8. eCollection 2019.

Abstract

BACKGROUND

is one of the most important oilseed crops, and can supply considerable amounts of edible oil as well as provide raw materials for the production of biodiesel in the biotechnology industry. Lysophosphatidic acid acyltransferase (LPAT), a key enzyme in the Kennedy pathway, catalyses fatty acid chains into 3-phosphoglycerate and promotes further production of oil in the form of triacylglycerol. However, because is an allotetraploid with two subgenomes, the precise genes which involved in oil production remain unclear due to the intractability of efficiently knocking out all copies with high genetic redundancy. Therefore, a robust gene editing technology is necessary for gene function analysis.

RESULTS

An efficient gene editing technology was developed for the allotetraploid plant using the CRISPR-Cas9 system. Previous studies showed poor results in either on-target or off-target activity in . In the present study, four single-gRNAs and two multi-gRNAs were deliberately designed from the conserved coding regions of which has seven homologous genes, and , which has four homologous genes. The mutation frequency was found to range from 17 to 68%, while no mutation was observed in the putative off-target sites. The seeds of the 2/5 mutant were wizened and showed enlarged oil bodies, disrupted distribution of protein bodies and increased accumulation of starch in mature seeds. The oil content decreased, with an average decrease of 32% for lines and 29% for lines in single-gRNA knockout lines, and a decline of 24% for mutant lines (i.e., g123) and 39% for / double mutant lines (i.e., g134) in multi-gRNA knockout lines.

CONCLUSIONS

Seven homologous genes and four homologous genes were cleaved completely using the CRISPR-Cas9 system, which indicated that it is effective for editing all homologous genes in allotetraploid rapeseed, despite the relatively low sequence identities of both gene families. The size of the oil bodies increased significantly while the oil content decreased, confirming that and play a role in oil biosynthesis. The present study lays a foundation for further oil production improvement in oilseed crop species.

摘要

背景

油菜是最重要的油料作物之一,能提供大量食用油,还为生物技术产业生产生物柴油提供原料。溶血磷脂酸酰基转移酶(LPAT)是肯尼迪途径中的关键酶,催化脂肪酸链转化为3-磷酸甘油,并促进以三酰甘油形式进一步合成油脂。然而,由于油菜是具有两个亚基因组的异源四倍体,由于难以有效敲除所有具有高遗传冗余性的拷贝,参与油脂合成的精确基因仍不清楚。因此,强大的基因编辑技术对于基因功能分析是必要的。

结果

利用CRISPR-Cas9系统为异源四倍体植物油菜开发了一种高效的基因编辑技术。先前的研究表明,在油菜中进行基因编辑时,无论是靶向活性还是脱靶活性都较差。在本研究中,从油菜中具有7个同源基因的保守编码区以及具有4个同源基因的保守编码区特意设计了4个单导向RNA(single-gRNAs)和2个多导向RNA(multi-gRNAs)。发现突变频率在17%至68%之间,而在假定的脱靶位点未观察到突变。2/5突变体的种子干瘪,成熟种子中油体增大、蛋白体分布紊乱且淀粉积累增加。油脂含量下降,单导向RNA敲除系中,油菜品系平均下降32%,甘蓝型油菜品系平均下降29%;多导向RNA敲除系中,突变体系(即g123)下降24%,/双突变体系(即g134)下降39%。

结论

利用CRISPR-Cas9系统完全切割了7个油菜同源基因和4个甘蓝型油菜同源基因,这表明尽管两个基因家族的序列同一性相对较低,但该系统对于编辑异源四倍体油菜中的所有同源基因是有效的。油体大小显著增加而油脂含量下降,证实了油菜和甘蓝型油菜在油脂生物合成中发挥作用。本研究为进一步提高油料作物的油脂产量奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e519/6753616/09477b80c9e5/13068_2019_1567_Fig1_HTML.jpg

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