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Plant gene expression control using genome- and epigenome-editing technologies

机译:采用基因组和外膜内杂志编辑技术的植物基因表达控制

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In this review, we present some specific examples of plant species only where modulation of gene regulation has been achieved via genome-editing and epigenome-editing technologies. Among genome-editing tools used in plants are zinc-finger nucleases inmaize (lea mays L); transcription activator-like effector nucleases in rice (Oryza sativa L), sugarcane (Saccharum spp.), and wheat (Triticum aestivum L); and clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9(Cas9) in O. sativa and tomato (Solanum lycopersicum L). A large number of epigenome-editing tools based on small RNAs have been employed for controlling plant gene expression in thale cress (Arabidopsis thaliana), tobacco (Nicotiana benthamiana), O. sativa, potato {Solanum tuberosum), and Z. mays. RNAi-based tools have been used in A. thaliana; RNAndirected DNA Methylation (RdDM) in A. thaliana; and RdDM involving transge-nically produced exogenous small interfering RNAs in 0. sativa. Site-specific DNA-binding proteins that have been successfully repurposed to function as DNA-binding domains of epigenome-editing tools include zinc-finger proteins, transcription activatorlike effectors, and dead Cas9 complexed with single-guide RNA. Zinc-finger-based epigenome-editing tools have been applied in A. thaliana and 0. sativa; and transcription activator-like effector and dead Cas9-based tools in 0. sativa and A. thaliana, respectively. Targeting-induced-local-lesions-in-genomes approach has beenemployed in muskmelon {Cucumis melo). Quantitative trait loci (QTL) were epigenetically modified in A. thaliana and 0. sativa. In vitro tissue culture-based epigenome-editing DNA and/or histone modifications have been achieved in Caribbean agave {Agave angustifolia), Henequen (Agave fourcroydes), A. thaliana, common tobacco (Nicotiana tabacum), O. sativa, pine (Pinus radiata), and Z. mays.
机译:在本文中,我们仅介绍了植物物种的一些具体实例,仅通过基因组编辑和外观蛋白酶编辑技术已经实现了基因调节的调节。在植物中使用的基因组编辑工具中是锌 - 手指核酸酶(Lea Mays L);转录活化剂样效应核酸核酸核酸酶(Oryza sativa L),甘蔗(Saccharum SPP。)和小麦(Triticum aestivum L);并在O.苜蓿和番茄(Solanum Lycopersicum L)中定期聚集在O. Sativa和Tomato(Solanum Lycopersicum L)中的间隙中的短语重复(CASRPr)/ Crism相关蛋白质9(Cas9)。基于小RNA的大量表述编辑编辑工具已经用于控制Thale Cress(Arabidopsis Thaliana),烟草(Nicotiana Benthamiana),O. sativa,马铃薯(Solanum Tuberosum)和Z.Mays中的植物基因表达。基于RNAI的工具已在A. Thaliana中使用;在A. Thaliana中的RNAndived DNA甲基化(RDDM);并且RDDM涉及转换的外源性小干扰RNA在0.Sativa。已经成功重新批准的特异性DNA结合蛋白作为表观蛋白酶编辑工具的DNA结合结构域包括锌指蛋白,转录活化剂样效应和与单引导RNA络合的死Cas9。基于锌 - 手指的外延簇形式编辑工具已应用于A. Thaliana和0.苜蓿;和转录活化剂样效应和基于死亡Cas9的基于死亡Cas9的工具。靶向诱导的局部病灶 - 基因因子方法已经播放在Muskmelon {Cucumis Melo)中。定量性状基因座(QTL)在拟南芥和0.苜蓿中进行了表现出外观修饰。在基于体外​​组织培养的外蛋白编辑DNA和/或组蛋白修饰已经在加勒比龙舌兰{龙舌兰羚羊),纯净(龙舌兰四晶),A.本地人,常见的烟草(Nicotiana Tabacum),O. Sativa,Pine(Pinus radiata)和z. mays。

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