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插入、移除或替换:一种使用CRISPR/Cas9的高度先进的基因组编辑系统。

Insert, remove or replace: A highly advanced genome editing system using CRISPR/Cas9.

作者信息

Ceasar S Antony, Rajan Vinothkumar, Prykhozhij Sergey V, Berman Jason N, Ignacimuthu S

机构信息

Division of Plant Biotechnology, Entomology Research Institute, Loyola College, Chennai, India; Centre for Plant Sciences and School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK.

Department of Microbiology and Immunology, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Biochim Biophys Acta. 2016 Sep;1863(9):2333-44. doi: 10.1016/j.bbamcr.2016.06.009. Epub 2016 Jun 24.


DOI:10.1016/j.bbamcr.2016.06.009
PMID:27350235
Abstract

The clustered, regularly interspaced, short palindromic repeat (CRISPR) and CRISPR associated protein 9 (Cas9) system discovered as an adaptive immunity mechanism in prokaryotes has emerged as the most popular tool for the precise alterations of the genomes of diverse species. CRISPR/Cas9 system has taken the world of genome editing by storm in recent years. Its popularity as a tool for altering genomes is due to the ability of Cas9 protein to cause double-stranded breaks in DNA after binding with short guide RNA molecules, which can be produced with dramatically less effort and expense than required for production of transcription-activator like effector nucleases (TALEN) and zinc-finger nucleases (ZFN). This system has been exploited in many species from prokaryotes to higher animals including human cells as evidenced by the literature showing increasing sophistication and ease of CRISPR/Cas9 as well as increasing species variety where it is applicable. This technology is poised to solve several complex molecular biology problems faced in life science research including cancer research. In this review, we highlight the recent advancements in CRISPR/Cas9 system in editing genomes of prokaryotes, fungi, plants and animals and provide details on software tools available for convenient design of CRISPR/Cas9 targeting plasmids. We also discuss the future prospects of this advanced molecular technology.

摘要

成簇规律间隔短回文重复序列(CRISPR)及其相关蛋白9(Cas9)系统最初是作为原核生物的一种适应性免疫机制被发现的,如今已成为用于精准改变多种物种基因组的最流行工具。近年来,CRISPR/Cas9系统在基因组编辑领域掀起了一场风暴。它作为一种基因组改变工具广受欢迎,是因为Cas9蛋白与短引导RNA分子结合后能够在DNA中产生双链断裂,而生产这种短引导RNA分子所付出的努力和成本比生产转录激活样效应核酸酶(TALEN)和锌指核酸酶(ZFN)要少得多。正如文献所示,从原核生物到包括人类细胞在内的高等动物等许多物种都已应用了该系统,这表明CRISPR/Cas9技术日益成熟、操作愈发简便,且适用的物种种类也不断增加。这项技术有望解决生命科学研究(包括癌症研究)中面临的几个复杂分子生物学问题。在本综述中,我们重点介绍了CRISPR/Cas9系统在原核生物、真菌、植物和动物基因组编辑方面的最新进展,并详细介绍了可用于方便设计CRISPR/Cas9靶向质粒的软件工具。我们还讨论了这种先进分子技术的未来前景。

相似文献

[1]
Insert, remove or replace: A highly advanced genome editing system using CRISPR/Cas9.

Biochim Biophys Acta. 2016-9

[2]
CRISPR/Cas9: an advanced tool for editing plant genomes.

Transgenic Res. 2016-10

[3]
CRISPR-Cas systems: ushering in the new genome editing era.

Bioengineered. 2018

[4]
Various Aspects of a Gene Editing System-CRISPR-Cas9.

Int J Mol Sci. 2020-12-16

[5]
Temperature effect on CRISPR-Cas9 mediated genome editing.

J Genet Genomics. 2017-3-30

[6]
CRISPR/Cas9-Based Genome Editing in Plants.

Prog Mol Biol Transl Sci. 2017

[7]
Review of CRISPR/Cas9 sgRNA Design Tools.

Interdiscip Sci. 2018-4-11

[8]
Gene Editing With TALEN and CRISPR/Cas in Rice.

Prog Mol Biol Transl Sci. 2017

[9]
CRISPR-Cas9 system: A new-fangled dawn in gene editing.

Life Sci. 2019-7-8

[10]
CRISPR/Cas9 gene-editing strategies in cardiovascular cells.

Cardiovasc Res. 2020-4-1

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CRISPR/Cas-Mediated Optimization of Soybean Shoot Architecture for Enhanced Yield.

Int J Mol Sci. 2025-8-16

[2]
Investigating the Efficacy of the CRISPR/Cas9 Gene-Editing System for Targeting the HBB FSC 36-37 (-T) Mutation Locus in Hematopoietic Stem Cells.

Mol Biotechnol. 2025-7-17

[3]
Genome editing in maize and sorghum: A comprehensive review of CRISPR/Cas9 and emerging technologies.

Plant Genome. 2025-6

[4]
Rethinking progress: harmonizing the discourse on genetically modified crops.

Front Plant Sci. 2025-3-21

[5]
Protocol for generating splice isoform-specific mouse mutants using CRISPR-Cas9 and a minigene splicing reporter.

STAR Protoc. 2025-3-21

[6]
Efficient small fragment sequencing of human, cattle, and bison miRNA, small RNA, or csRNA-seq libraries using AVITI.

BMC Genomics. 2024-11-29

[7]
Exploring the role of FAT genes in Solanaceae species through genome-wide analysis and genome editing.

Plant Genome. 2024-12

[8]
A PLA2 deletion mutant using CRISPR/Cas9 coupled to RNASeq reveals insect immune genes associated with eicosanoid signaling.

PLoS One. 2024-7-17

[9]
Designing Epigenome Editors: Considerations of Biochemical and Locus Specificities.

Methods Mol Biol. 2024

[10]
The potential of genome editing to create novel alleles of resistance genes in rice.

Front Genome Ed. 2024-6-11

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