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通过将大分子直接导入水稻卵细胞和受精卵实现基因表达与基因组编辑系统

Gene Expression and Genome Editing Systems by Direct Delivery of Macromolecules Into Rice Egg Cells and Zygotes.

作者信息

Toda Erika, Okamoto Takashi

机构信息

Department of Biological Sciences, Tokyo Metropolitan University, Hachioji, Tokyo, 192-0397, Japan.

出版信息

Bio Protoc. 2020 Jul 20;10(14):e3681. doi: 10.21769/BioProtoc.3681.

Abstract

Polyethylene glycol calcium (PEG-Ca)-mediated transfection allows rapid and efficient examination to analyze diverse cellular functions of genes of interest. In plant cells, macromolecules, such as DNA, RNA and protein, are delivered into protoplasts derived from somatic tissues or calli via PEG-Ca transfection. To broaden and develop the scope of investigations using plant gametes and zygotes, a procedure for direct delivery of macromolecules into these cells has recently been established using PEG-Ca transfection. This PEG-Ca-mediated delivery into rice egg cells/zygotes consists of four microtechniques, (i) isolation of gametes, (ii) production of zygotes by electrofusion of gametes, (iii) PEG-Ca-mediated delivery of macromolecules into isolated egg cells or produced zygotes, and (iv) culture and subsequent analyses of the transfected egg cells/zygotes. Because the full protocol for microtechniques (i) and (ii) have already been reported in Toda , 2016 , microtechniques (iii) and (iv) are mainly described in this protocol.

摘要

聚乙二醇钙(PEG-Ca)介导的转染能够快速有效地进行检测,以分析感兴趣基因的多种细胞功能。在植物细胞中,DNA、RNA和蛋白质等大分子通过PEG-Ca转染被导入源自体细胞组织或愈伤组织的原生质体中。为了拓宽和拓展利用植物配子和受精卵进行研究的范围,最近已建立了一种使用PEG-Ca转染将大分子直接导入这些细胞的方法。这种PEG-Ca介导的向水稻卵细胞/受精卵中的导入由四项显微技术组成:(i)配子的分离;(ii)通过配子电融合产生受精卵;(iii)PEG-Ca介导将大分子导入分离出的卵细胞或产生的受精卵;(iv)对转染的卵细胞/受精卵进行培养及后续分析。由于显微技术(i)和(ii)的完整方案已在Toda,2016年报道过,本方案主要描述显微技术(iii)和(iv)。

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