Transgenesis in microalga Chlamydomonas reinhardtii: current approaches

Pavel A. Virolainen, Elena M. Chekunova
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Abstract

Microalgae are a rich source of biologically active substances of natural origin, which have potential for use in pharmaceutical, agricultural, food and industrial production. Genetic engineering of microalgae opens up great prospects for creating improved strains that produce various food additives, commercial enzymes, as well as proteins for therapeutic purposes – antibodies, hormones and vaccines. Chlamydomonas reinhardtii P.A.Dang. is a unicellular green alga, a reference organism for studying the genetics of photosynthesis and developing new genetic engineering approaches in microalgae. The advantages of C. reinhardtii include the ability to transform all three of its genomes (nuclear, mitochondrial and chloroplast), low cost and ease of cultivation, safety for humans and the presence of a system for post-translational modification of proteins, which makes this organism a potential platform for use in biotechnology. Over the past few years, significant advances have been made in transgenesis of C. reinhardtii, including the use of new techniques based on the CRISPR/Cas9 genome editing technology. In this review, we summarize the available information on current approaches to transgenesis of the unicellular green alga C. reinhardtii: 1) general principles of transgenic constructs design for transformation of the nuclear and chloroplast genome, 2) popular selection markers used, 3) methods of cell transformation, 4) methods of genome editing using the CRISPR/Cas9 system.
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微藻类衣藻的转基因:当前的方法
微藻是天然生物活性物质的丰富来源,具有用于制药、农业、食品和工业生产的潜力。微藻类的基因工程为创造改良品系开辟了广阔的前景,这些改良品系可以生产各种食品添加剂、商业酶以及用于治疗目的的蛋白质--抗体、激素和疫苗。莱茵衣藻(Chlamydomonas reinhardtii P.A.Dang.)是一种单细胞绿藻,是研究光合作用遗传学和开发新的微藻类遗传工程方法的参考生物。C. reinhardtii 的优势包括能够转化其全部三个基因组(核、线粒体和叶绿体)、成本低、易于培养、对人类安全以及存在蛋白质翻译后修饰系统,这使得该生物体成为生物技术的潜在应用平台。在过去几年中,C. reinhardtii 的转基因研究取得了重大进展,包括使用基于 CRISPR/Cas9 基因组编辑技术的新技术。在这篇综述中,我们总结了有关目前单细胞绿藻 C. reinhardtii 转基因方法的现有信息:1)设计转基因构建体以转化核基因组和叶绿体基因组的一般原则;2)常用的选择标记;3)细胞转化方法;4)使用 CRISPR/Cas9 系统进行基因组编辑的方法。
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