聚类规则间隔短回文重复/Cas9基因工程:机器人基因手术。

Kaivalya Deshpande, Arpita Vyas, Archana Balakrishnan, Dinesh Vyas
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引用次数: 14

摘要

CRISPR/Cas9作为一种利用细菌内源性免疫防御系统的新技术,已经超越了DNA工程,进入了一个更加实用和临床有效的领域。利用可编程sgRNA序列和核酸酶,该系统有效地在整个生物体内的靶基因中引入双链断裂。CRISPR的应用范围从生物医学到药物开发和表观遗传修饰。研究表明,CRISPR介导的多种致瘤基因和效应蛋白与结肠癌有关。这项技术大大扩展了基因操作的范围,并允许对结肠癌以及各种其他恶性肿瘤进行增强建模。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clustered Regularly Interspaced Short Palindromic Repeats/Cas9 Genetic Engineering: Robotic Genetic Surgery.

Clustered Regularly Interspaced Short Palindromic Repeats/Cas9 Genetic Engineering: Robotic Genetic Surgery.

Clustered Regularly Interspaced Short Palindromic Repeats/Cas9 Genetic Engineering: Robotic Genetic Surgery.

As a novel technology that utilizes the endogenous immune defense system in bacteria, CRISPR/Cas9 has transcended DNA engineering into a more pragmatic and clinically efficacious field. Using programmable sgRNA sequences and nucleases, the system effectively introduces double strand breaks in target genes within an entire organism. The applications of CRISPR range from biomedicine to drug development and epigenetic modification. Studies have demonstrated CRISPR mediated targeting of various tumorigenic genes and effector proteins known to be involved in colon carcinomas. This technology significantly expands the scope of gene manipulation and allows for an enhanced modeling of colon cancers, as well as various other malignancies.

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