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CRISPR/Cas9 技术:应用与人类疾病建模。

CRISPR/Cas9 Technology: Applications and Human Disease Modeling.

机构信息

Molecular Cytogenetics and Genome Engineering Group, Centro Nacional Investigaciones Oncológicas (CNIO), Madrid, Spain.

Molecular Cytogenetics and Genome Engineering Group, Centro Nacional Investigaciones Oncológicas (CNIO), Madrid, Spain.

出版信息

Prog Mol Biol Transl Sci. 2017;152:23-48. doi: 10.1016/bs.pmbts.2017.09.002. Epub 2017 Oct 31.

Abstract

The CRISPR/Cas9 system development has revolutionized the field of genome engineering through the efficient creation of targeted breaks in the DNA of almost any organism and cell type, opening an avenue for a wide range of applications in biomedical research and medicine. Apart from gene edition through knock-in or knock-out approaches, CRISPR/Cas9 technology has been used for many other purposes, including regulation of endogenous gene expression, epigenome editing, live-cell imaging of chromosomal loci, edition of RNA and high-throughput screening. With all those technological improvements, CRISPR/Cas9 system has broadened the number of alternatives for studying gene function and the generation of more accurate disease models. Although many mechanistic questions remain to be answered and several challenges have yet to be addressed, the use of CRISPR/Cas9-based genome engineering technologies will increase our knowledge of disease processes and their treatment in the near future.

摘要

CRISPR/Cas9 系统的发展通过在几乎任何生物体和细胞类型的 DNA 中高效地产生靶向断裂,彻底改变了基因组工程领域,为生物医学研究和医学中的广泛应用开辟了道路。除了通过敲入或敲除方法进行基因编辑外,CRISPR/Cas9 技术还被用于许多其他用途,包括内源性基因表达的调控、表观基因组编辑、染色体位置的活细胞成像、RNA 的编辑和高通量筛选。随着所有这些技术的改进,CRISPR/Cas9 系统为研究基因功能和生成更精确的疾病模型提供了更多的选择。尽管仍有许多机制问题有待解答,并且仍有一些挑战需要解决,但基于 CRISPR/Cas9 的基因组工程技术的使用将在不久的将来增加我们对疾病过程及其治疗的了解。

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