a Faculty of Agriculture; Cairo University ; Cairo , Egypt ;
b Tuskegee University ; Tuskegee , AL USA.
GM Crops Food. 2015;6(4):183-205. doi: 10.1080/21645698.2015.1129937.
Genome or gene editing includes several new techniques to help scientists precisely modify genome sequences. The techniques also enables us to alter the regulation of gene expression patterns in a pre-determined region and facilitates novel insights into the functional genomics of an organism. Emergence of genome editing has brought considerable excitement especially among agricultural scientists because of its simplicity, precision and power as it offers new opportunities to develop improved crop varieties with clear-cut addition of valuable traits or removal of undesirable traits. Research is underway to improve crop varieties with higher yields, strengthen stress tolerance, disease and pest resistance, decrease input costs, and increase nutritional value. Genome editing encompasses a wide variety of tools using either a site-specific recombinase (SSR) or a site-specific nuclease (SSN) system. Both systems require recognition of a known sequence. The SSN system generates single or double strand DNA breaks and activates endogenous DNA repair pathways. SSR technology, such as Cre/loxP and Flp/FRT mediated systems, are able to knockdown or knock-in genes in the genome of eukaryotes, depending on the orientation of the specific sites (loxP, FLP, etc.) flanking the target site. There are 4 main classes of SSN developed to cleave genomic sequences, mega-nucleases (homing endonuclease), zinc finger nucleases (ZFNs), transcriptional activator-like effector nucleases (TALENs), and the CRISPR/Cas nuclease system (clustered regularly interspaced short palindromic repeat/CRISPR-associated protein). The recombinase mediated genome engineering depends on recombinase (sub-) family and target-site and induces high frequencies of homologous recombination. Improving crops with gene editing provides a range of options: by altering only a few nucleotides from billions found in the genomes of living cells, altering the full allele or by inserting a new gene in a targeted region of the genome. Due to its precision, gene editing is more precise than either conventional crop breeding methods or standard genetic engineering methods. Thus this technology is a very powerful tool that can be used toward securing the world's food supply. In addition to improving the nutritional value of crops, it is the most effective way to produce crops that can resist pests and thrive in tough climates. There are 3 types of modifications produced by genome editing; Type I includes altering a few nucleotides, Type II involves replacing an allele with a pre-existing one and Type III allows for the insertion of new gene(s) in predetermined regions in the genome. Because most genome-editing techniques can leave behind traces of DNA alterations evident in a small number of nucleotides, crops created through gene editing could avoid the stringent regulation procedures commonly associated with GM crop development. For this reason many scientists believe plants improved with the more precise gene editing techniques will be more acceptable to the public than transgenic plants. With genome editing comes the promise of new crops being developed more rapidly with a very low risk of off-target effects. It can be performed in any laboratory with any crop, even those that have complex genomes and are not easily bred using conventional methods.
基因组或基因编辑包括几种新技术,可帮助科学家精确地修改基因组序列。这些技术还使我们能够改变预定区域中基因表达模式的调节,并促进对生物体功能基因组学的新认识。基因组编辑的出现引起了相当大的兴奋,特别是在农业科学家中间,因为它简单、精确和强大,为开发具有明显附加值的改良作物品种提供了新的机会,或者去除不需要的特性。研究正在进行中,以提高产量、增强抗胁迫能力、提高疾病和害虫抗性、降低投入成本和增加营养价值。基因组编辑涵盖了多种工具,包括使用特定部位重组酶(SSR)或特定部位核酸酶(SSN)系统。这两个系统都需要识别已知的序列。SSN 系统会产生单链或双链 DNA 断裂,并激活内源性 DNA 修复途径。SSR 技术,如 Cre/loxP 和 Flp/FRT 介导的系统,能够根据靶位点侧翼特定位点(loxP、FLP 等)的方向,敲低或敲入真核生物基因组中的基因。已经开发出 4 种主要的 SSN 类来切割基因组序列,即巨型核酶(归巢内切酶)、锌指核酸酶(ZFNs)、转录激活因子样效应核酸酶(TALENs)和 CRISPR/Cas 核酸酶系统(成簇的规则间隔的短回文重复序列/CRISPR 相关蛋白)。重组酶介导的基因组工程依赖于重组酶(亚)家族和靶位点,并诱导同源重组的高频发生。通过基因编辑改良作物提供了一系列选择:通过改变活细胞基因组中数十亿个碱基中的少数几个碱基,改变完整的等位基因或在基因组的靶向区域插入新基因。由于其精确性,基因编辑比传统的作物育种方法或标准的遗传工程方法更精确。因此,这项技术是一种非常强大的工具,可以用于确保世界粮食供应。除了提高作物的营养价值外,它还是生产能够抵抗害虫并在恶劣气候中茁壮成长的作物的最有效方法。基因组编辑产生了 3 种类型的修饰;I 型包括改变少数几个核苷酸,II 型涉及用预先存在的等位基因替换一个等位基因,III 型允许在基因组的预定区域插入新基因(多个)。由于大多数基因组编辑技术可以在少数核苷酸中留下明显的 DNA 改变痕迹,因此通过基因编辑产生的作物可以避免与 GM 作物开发通常相关的严格监管程序。出于这个原因,许多科学家认为,通过更精确的基因编辑技术改良的植物比转基因植物更容易被公众接受。基因组编辑带来了新作物开发速度更快、脱靶效应风险极低的希望。它可以在任何实验室中对任何作物进行操作,即使是那些基因组复杂且不易用传统方法进行育种的作物。