The Revolution Continues: Newly Discovered Systems Expand the CRISPR-Cas Toolkit

清脆的 生物 计算生物学 基因组编辑 Cas9 效应器 核酸内切酶 遗传学 基因组工程 DNA 基因 细胞生物学
作者
Karthik Murugan,Kesavan Babu,Ramya Sundaresan,Rakhi Rajan,Dipali G. Sashital
出处
期刊:Molecular Cell [Elsevier BV]
卷期号:68 (1): 15-25 被引量:205
标识
DOI:10.1016/j.molcel.2017.09.007
摘要

CRISPR-Cas systems defend prokaryotes against bacteriophages and mobile genetic elements and serve as the basis for revolutionary tools for genetic engineering. Class 2 CRISPR-Cas systems use single Cas endonucleases paired with guide RNAs to cleave complementary nucleic acid targets, enabling programmable sequence-specific targeting with minimal machinery. Recent discoveries of previously unidentified CRISPR-Cas systems have uncovered a deep reservoir of potential biotechnological tools beyond the well-characterized Type II Cas9 systems. Here we review the current mechanistic understanding of newly discovered single-protein Cas endonucleases. Comparison of these Cas effectors reveals substantial mechanistic diversity, underscoring the phylogenetic divergence of related CRISPR-Cas systems. This diversity has enabled further expansion of CRISPR-Cas biotechnological toolkits, with wide-ranging applications from genome editing to diagnostic tools based on various Cas endonuclease activities. These advances highlight the exciting prospects for future tools based on the continually expanding set of CRISPR-Cas systems. CRISPR-Cas systems defend prokaryotes against bacteriophages and mobile genetic elements and serve as the basis for revolutionary tools for genetic engineering. Class 2 CRISPR-Cas systems use single Cas endonucleases paired with guide RNAs to cleave complementary nucleic acid targets, enabling programmable sequence-specific targeting with minimal machinery. Recent discoveries of previously unidentified CRISPR-Cas systems have uncovered a deep reservoir of potential biotechnological tools beyond the well-characterized Type II Cas9 systems. Here we review the current mechanistic understanding of newly discovered single-protein Cas endonucleases. Comparison of these Cas effectors reveals substantial mechanistic diversity, underscoring the phylogenetic divergence of related CRISPR-Cas systems. This diversity has enabled further expansion of CRISPR-Cas biotechnological toolkits, with wide-ranging applications from genome editing to diagnostic tools based on various Cas endonuclease activities. These advances highlight the exciting prospects for future tools based on the continually expanding set of CRISPR-Cas systems.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
1秒前
Pann发布了新的文献求助10
1秒前
天晴应助菠萝汁采纳,获得10
1秒前
北蓝完成签到,获得积分10
2秒前
2秒前
忧虑的凛发布了新的文献求助10
3秒前
隐形曼青应助伍寒烟采纳,获得10
3秒前
5秒前
挖掘机应助cy32522采纳,获得200
5秒前
苏神吊打有机应助元2333采纳,获得10
6秒前
7秒前
ttt发布了新的文献求助10
7秒前
完美世界应助liuxi采纳,获得20
8秒前
丘比特应助醉熏的问丝采纳,获得10
9秒前
Owen应助efkwiefh采纳,获得30
10秒前
Owen应助羲和采纳,获得10
10秒前
彭于晏应助默默的惜灵采纳,获得10
10秒前
nikky977发布了新的文献求助10
11秒前
香潘潘的楠瓜完成签到,获得积分10
12秒前
12秒前
12秒前
赘婿应助诚心无颜采纳,获得30
12秒前
msf0073完成签到,获得积分20
14秒前
洗洗完成签到,获得积分10
14秒前
14秒前
ttong完成签到,获得积分10
14秒前
czm完成签到,获得积分10
14秒前
泡泡完成签到 ,获得积分10
15秒前
15秒前
15秒前
15秒前
16秒前
Stefan发布了新的文献求助20
16秒前
Jeri完成签到 ,获得积分10
17秒前
东方元语应助BCLee采纳,获得20
18秒前
忧虑的凛完成签到,获得积分10
18秒前
药学生完成签到,获得积分10
18秒前
18秒前
falunwen发布了新的文献求助10
18秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Römisch-Germanische Forschungen 1000
APA handbook of comparative psychology: Basic concepts, methods, neural substrate, and behavior 1000
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
The fast track to determining transfer functions of linear circuits: The student guide 500
The Analytical and Numerical Solution of Electric and Magnetic Fields 500
Discerning Saints: Moralization of Intrinsic Motivation and Selective Prosociality at Work 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7607209
求助须知:如何正确求助?哪些是违规求助? 9183089
关于积分的说明 19669213
捐赠科研通 7181430
什么是DOI,文献DOI怎么找? 3269748
关于科研通互助平台的介绍 2433595
邀请新用户注册赠送积分活动 2264072