CRISPR-Cas介导的基因组工程综述

T. G. Bhuvana, N. Ranjitha
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引用次数: 0

摘要

遗传疾病在全世界3-5%的新生儿中流行,估计造成约50%的儿童死亡。开发一种高效、规范的定制基因组修饰系统来治疗这些疾病一直是人们感兴趣的领域。随着时间的推移,基于ZFN或TALENS等可编程核酸酶的不同编辑技术已经出现,但总的来说,CRISPR-Cas作为一种从实验室到临床实践的改变工具已经取得了重大进展。CRISPR-Cas是在原核生物中发现的一种免疫系统,它使生物体能够识别并摧毁任何入侵的遗传元素。CRISPR的这一功能特性在诊断、农业和治疗等不同学科中开辟了大量的应用。因此,在这里,回顾试图讨论起源,机制相关的CRISPR和应用以及挑战。
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Overview of CRISPR-Cas Mediated Genome Engineering
Genetic diseases are prevailing in 3-5% of new-born worldwide and estimated to cause around 50% of child deaths. The development of efficient and regulated system for customizing genome modifications to treat such disorders has been the zone of interest. Over time, different editing techniques have emerged based on programmable nucleases such as ZFN or TALENS but among all, CRISPR-Cas has significantly progressed as alteration tool from bench to clinical practices. CRISPR-Cas is an immune system discovered in prokaryotes that enables organism to recognize and destroy any invading genetic elements. This functional property of CRISPR has opened up plethora of applications across different disciplines such as diagnostics, agriculture and therapeutics. So here, the review attempt to discuss origin, mechanisms pertinent to CRISPR and applications along with challenges concerning them.
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