首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Targeted mutagenesis using zinc-finger nucleases in Arabidopsis.
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Targeted mutagenesis using zinc-finger nucleases in Arabidopsis.

机译:使用锌指核酸酶在拟南芥中定向诱变。

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Targeted mutagenesis is an essential tool of reverse genetics that could be used experimentally to investigate basic plant biology or modify crop plants for improvement of important agricultural traits. Although targeted mutagenesis is routine in several model organisms including yeast and mouse, efficient and widely usable methods to generate targeted modifications in plant genes are not currently available. In this study we investigated the efficacy of a targeted-mutagenesis approach based on zinc-finger nucleases (ZFNs). In this procedure, ZFNs are used to generate double-strand breaks at specific genomic sites, and subsequent repair produces mutations at the break site. To determine whether ZFNs can cleave and induce mutations at specific sites within higher plant genomes, we introduced a construct carrying both a ZFN gene, driven by a heat-shock promoter, and its target into the Arabidopsis genome. Induction of ZFN expression by heat shock during seedling development resulted in mutations at the ZFN recognition sequence at frequencies as high as 0.2 mutations per target. Of 106 ZFN-induced mutations characterized, 83 (78%) were simple deletions of 1-52 bp (median of 4 bp), 14 (13%) were simple insertions of 1-4 bp, and 9 (8%) were deletions accompanied by insertions. In 10% of induced individuals, mutants were present in the subsequent generation, thus demonstrating efficient transmission of the ZFN-induced mutations. These data indicate that ZFNs can form the basis of a highly efficient method for targeted mutagenesis of plant genes.
机译:定向诱变是反向遗传学的重要工具,可用于实验研究基础植物生物学或修饰农作物以改善重要的农业性状。尽管靶向诱变在包括酵母和小鼠在内的几种模式生物中是常规的,但是目前尚无有效且广泛使用的方法来在植物基因中产生靶向修饰。在这项研究中,我们研究了基于锌指核酸酶(ZFN)的靶向诱变方法的功效。在该程序中,ZFN用于在特定基因组位点产生双链断裂,随后的修复在断裂位点产生突变。为了确定ZFN是否可以在高等植物基因组内的特定位点切割并诱导突变,我们将携带热休克启动子驱动的ZFN基因及其靶标的结构引入拟南芥基因组。幼苗发育过程中热激诱导的ZFN表达导致ZFN识别序列的突变频率高达每个靶标0.2个突变。在106个ZFN诱导的突变中,有83个(78%)是1-52 bp的简单缺失(中位数4 bp),14个(13%)是1-4 bp的简单插入,9(8%)是缺失伴随插入。在10%的诱导个体中,突变体存在于随后的世代中,因此证明ZFN诱导的突变有效传递。这些数据表明ZFN可以构成针对植物基因的定向诱变的高效方法的基础。

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