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Gene targeting and editing in crop plants: a new era of precision opportunities

机译:作物基因靶向和编辑:精准机遇的新时代

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With increasing global food demands in the face of challenging biotic and abiotic pressures on crop production, there is a vital need for good crop improvement strategies. Gene editing and gene targeting using designer nucleases are relatively new, sophisticated approaches that can be used for crop improvement. Designer nucleases are molecules that can be engineered to cleave virtually any endogenous DNA target sequence, making this technology inherently more powerful over current, essentially random mutation strategies. These molecules can also be used to promote targeted DNA insertions and homologous recombination. Further modifications of these molecules can convert them into designer transcription factors that can activate or suppress a gene of choice. Four designer nuclease platforms are currently available: meganucleases, zinc finger nucleases, TALENs and the more recently developed CRISPR/Cas9 system. All four of these systems have been shown to function in crop plants and have been used for site-specific gene targeting and gene editing. Herein, we describe the basis of each designer nuclease platform, highlighting the advantages and disadvantages of each, and give examples of their application in crop improvement.
机译:面对挑战性的生物和非生物作物生产压力,全球粮食需求不断增长,因此迫切需要制定良好的作物改良策略。使用设计者核酸酶的基因编辑和基因靶向是相对较新的复杂方法,可用于作物改良。设计者核酸酶是可以被工程化以切割几乎任何内源性DNA靶序列的分子,从而使得该技术在本质上比当前的,基本随机的突变策略更强大。这些分子也可用于促进靶向的DNA插入和同源重组。这些分子的进一步修饰可以将它们转换为可以激活或抑制所选基因的设计转录因子。当前有四个设计器核酸酶平台:大范围核酸酶,锌指核酸酶,TALEN和最近开发的CRISPR / Cas9系统。这些系统中的所有四个已显示在农作物中起作用,并已用于定点基因靶向和基因编辑。在这里,我们描述了每个设计者核酸酶平台的基础,强调了每个设计者的优缺点,并举例说明了它们在作物改良中的应用。

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