Liu Guoquan, Li Jieqing, Godwin Ian D
School of Agriculture and Food Sciences, The University of Queensland, Brisbane, QLD, Australia.
College of Agriculture, Anhui Science and Technology University, Fengyang, China.
Methods Mol Biol. 2019;1931:169-183. doi: 10.1007/978-1-4939-9039-9_12.
The advanced biotechnology CRISPR/Cas9 as a powerful genome editing tool has displayed great potential for improving important agronomic traits such as yield and quality. It has gained momentum worldwide for gene function research of plants in recent years. As for cereals, numerous studies of CRISPR/Cas9 have been reported predominately on rice and quite a few on other cereals including maize, wheat, and barley. In contrast, there are only a couple of reports on sorghum up to date. In this chapter, the CRISPR/Cas9 system has been investigated for sorghum genome editing through biolistic bombardment. Two target genes, cinnamyl alcohol dehydrogenase (CAD) and phytoene desaturase (PDS), have been investigated by CRISPR/Cas9 though bomboarment. Successful genome editing has been achieved within the sorghum genotype Tx430. Furthermore, sequencing PCR product of transgenic plants has confirmed that the CRISPR/Cas9 successfully edited the target gene in sorghum. Both homozygosis and heterozygosis editings of CAD gene have been confirmed in T primary transgenic lines through sequencing PCR products. T generation of CRISPR plants has been investigated as well. The results illustrated that the edited gene has passed down to next generation. More experiments, such as optimizing promoters for guide RNA (gRNA) and Cas9 in sorghum, are under investigation. Three factors were considered crucial elements to establish an efficient CRISPR/Cas9 system for genome editing in sorghum: (1) an efficient transformation system, (2) the design of targeted gene sequence for gRNA, (3) effective expression of CRISPR components including Cas9 and gRNA.
先进的生物技术CRISPR/Cas9作为一种强大的基因组编辑工具,在改善产量和品质等重要农艺性状方面显示出巨大潜力。近年来,它在全球植物基因功能研究中势头迅猛。对于谷类作物,大量关于CRISPR/Cas9的研究主要集中在水稻上,也有一些针对包括玉米、小麦和大麦在内的其他谷类作物。相比之下,迄今为止关于高粱的报道仅有寥寥几篇。在本章中,通过生物弹道轰击研究了CRISPR/Cas9系统对高粱基因组的编辑作用。通过轰击对肉桂醇脱氢酶(CAD)和八氢番茄红素去饱和酶(PDS)这两个靶基因进行了研究。在高粱基因型Tx430中实现了成功的基因组编辑。此外,转基因植物的PCR产物测序证实CRISPR/Cas9成功编辑了高粱中的靶基因。通过对PCR产物测序,在T代初级转基因系中证实了CAD基因的纯合和杂合编辑。对CRISPR植物的T代也进行了研究。结果表明编辑后的基因已传递到下一代。更多实验,如优化高粱中引导RNA(gRNA)和Cas9的启动子,正在进行中。建立高效的CRISPR/Cas9系统用于高粱基因组编辑时,有三个因素被认为是关键要素:(1)高效的转化系统,(2)gRNA靶向基因序列的设计,(3)包括Cas9和gRNA在内的CRISPR组件的有效表达。