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Genome engineering technologies for targeted genetic modification in plants
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作者 Wei Tang Anna Y. Tang 《Journal of Forestry Research》 SCIE CAS CSCD 2018年第4期875-887,共13页
Well-established targeted technologies to engi- neer genomes such as zinc-finger nuclease-based editing (ZFN), transcription activator-like effector nuclease-based editing (TALEN), and clustered regularly interspa... Well-established targeted technologies to engi- neer genomes such as zinc-finger nuclease-based editing (ZFN), transcription activator-like effector nuclease-based editing (TALEN), and clustered regularly interspaced short palindromic repeats and associated protein system-based editing (CRISPR/Cas) are proving to advance basic and applied research in numerous plant species. Compared with systems using ZFNs and TALENs, the most recently developed CRISPR/Cas system is more efficient due to its use of an RNA-guided nuclease to generate double-strand DNA breaks. To accelerate the applications of these technologies, we provide here a detailed overview of these systems, highlight the strengths and weaknesses of each, summarize research advances made with these technologies in model and crop plants, and discuss their applications in plant functional genomics. Such targeted approaches for genetically modifying plants will benefit agricultural production in the future. 展开更多
关键词 Double-stranded DNA break Genomeediting CRISPR system transcription activator-likeeffector nucleases Zinc-finger nucleases
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基因编辑技术的研究进展 被引量:5
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作者 李妤 赵红业 +2 位作者 崔勇 魏红江 李梅章 《生命科学研究》 CAS CSCD 2017年第3期268-274,共7页
功能缺失(loss of function)是研究基因功能及其相关表型最重要、最直接的方法和策略。基因编辑技术从开始的RNA干扰(RNA interference,RNAi)技术到近年发展起来的高效酶技术都得到了广泛的应用。这些高效酶技术包括锌指核酸酶(zinc fin... 功能缺失(loss of function)是研究基因功能及其相关表型最重要、最直接的方法和策略。基因编辑技术从开始的RNA干扰(RNA interference,RNAi)技术到近年发展起来的高效酶技术都得到了广泛的应用。这些高效酶技术包括锌指核酸酶(zinc finger nuclease,ZFN)技术、转录激活样效应物核酸酶(transcription activator-like effector nucleases,TALENs)技术和成簇的规律间隔的短回文重复序列系统(clustered regularly interspaced short palindromic repeats(CRISPR)/CRISPR-associated(Cas)9 system,CRISPR/Cas9)。除此之外,还有2016年发表的Ng Ago(Natronobacterium gregoryi Argonaute)编辑技术。近十年来,以CRISPR/Cas9为代表的基因编辑技术已经广泛应用于细胞水平和个体水平的基因功能敲除的研究。现就以上基因编辑技术的原理及最新进展进行综述,并重点介绍CRISPR/Cas9的技术原理以及该技术在建立基因敲除动物模型中的最新进展。 展开更多
关键词 基因敲除 RNA干扰(RNAI) 锌指核酸酶(ZFN) 转录激活样效应物核酸酶(TALENs) 成簇的规律间隔的短回文重复序列系统(CRISPR/Cas9) Argonaute内切酶
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