Fish Genetics and Biotechnology Division, ICAR - Central Institute of Freshwater Aquaculture, Bhubaneswar, Odisha, 751002, India.
Department of Biotechnology, Ministry of Science and Technology, CGO Complex, Block 3, Lodhi Road, New Delhi, 110003, India.
Transgenic Res. 2017 Oct;26(5):577-589. doi: 10.1007/s11248-017-0030-5. Epub 2017 Jul 5.
Advancements in the DNA sequencing technologies and computational biology have revolutionized genome/transcriptome sequencing of non-model fishes at an affordable cost. This has led to a paradigm shift with regard to our heightened understandings of structure-functional relationships of genes at a global level, from model animals/fishes to non-model large animals/fishes. Whole genome/transcriptome sequencing technologies were supplemented with the series of discoveries in gene editing tools, which are being used to modify genes at pre-determined positions using programmable nucleases to explore their respective in vivo functions. For a long time, targeted gene disruption experiments were mostly restricted to embryonic stem cells, advances in gene editing technologies such as zinc finger nuclease, transcriptional activator-like effector nucleases and CRISPR (clustered regulatory interspaced short palindromic repeats)/CRISPR-associated nucleases have facilitated targeted genetic modifications beyond stem cells to a wide range of somatic cell lines across species from laboratory animals to farmed animals/fishes. In this review, we discuss use of different gene editing tools and the strategic implications in fish species for basic and applied biology research.
DNA 测序技术和计算生物学的进步使得以可承受的成本对非模式鱼类进行基因组/转录组测序成为可能。这导致了一个范式转变,我们对全球范围内模型动物/鱼类和非模式大型动物/鱼类的基因结构-功能关系的理解得到了提高。全基因组/转录组测序技术与基因编辑工具的一系列发现相辅相成,这些工具正被用于使用可编程核酸酶在预定位置修饰基因,以探索它们各自的体内功能。长期以来,靶向基因敲除实验主要局限于胚胎干细胞,基因编辑技术的进步,如锌指核酸酶、转录激活因子样效应核酸酶和 CRISPR(成簇的规则间隔短回文重复序列)/CRISPR 相关核酸酶,使得靶向基因修饰超越了胚胎干细胞,能够在从实验室动物到养殖动物/鱼类的各种物种的广泛体细胞系中进行。在这篇综述中,我们讨论了不同基因编辑工具的使用及其在鱼类物种中的基础和应用生物学研究中的战略意义。