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CRISPR/Cas9: Nature’s gift to prokaryotes and an auspicious tool in genome editing

机译:CRISPR / CAS9:Nature的礼物到基因组编辑中的原始工具和吉祥工具

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摘要

Clustered regularly interspaced short palindromic repeats (CRISPR) is a family of DNA direct repeats found in many prokaryotic genomes. It was discovered in bacteria as their (adaptive) immune system against invading viruses. Cas9 is an endonuclease enzyme linked with the CRISPR system in bacteria. Bacteria use the Cas9 enzyme to chop viral DNA sequences by unwinding it and then finding the complementary base pairs to the guide RNA. CRISPR/Cas9 is a modern and powerful molecular biology approach that is widely used in genome engineering (to activate/repress gene expression). It can be used in vivo to cause targeted genome modifications with better efficiency as compared to meganucleases, zinc-finger nucleases and transcription activator-like effector nucleases. CRISPR/Cas9 is a simple, reliable, and rapid method for causing gene alterations that open new horizons of gene editing in a variety of living organisms, including humans, for the treatment of several diseases. In this short review, we explored the basic mechanisms underlying its working principles along with some of its current applications in a number of diverse fields.
机译:聚集的规则间隔短回文重复序列(CRISPR)是在许多原核基因组中发现的一个DNA直接重复序列家族。它是在细菌中发现的,作为他们抵抗入侵病毒的(适应性)免疫系统。Cas9是一种与细菌CRISPR系统相连的核酸内切酶。细菌利用Cas9酶将病毒DNA序列展开,然后找到与引导RNA互补的碱基对,从而切割病毒DNA序列。CRISPR/Cas9是一种现代而强大的分子生物学方法,广泛应用于基因组工程(激活/抑制基因表达)。与巨核酸酶、锌指核酸酶和转录激活物样效应核酸酶相比,它可以在体内以更好的效率进行靶向基因组修饰。CRISPR/Cas9是一种简单、可靠、快速的基因改变方法,为包括人类在内的多种生物的基因编辑开辟了新的视野,用于治疗多种疾病。在这篇简短的综述中,我们探讨了其工作原理背后的基本机制,以及目前在许多不同领域的一些应用。

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