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拟南芥质体基因组中的靶向C到T碱基编辑

Targeted C-to-T Base Editing in the Arabidopsis Plastid Genome.

作者信息

Nakazato Issei, Arimura Shin-Ichi

机构信息

Laboratory of Plant Molecular Genetics, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.

Japan Society for the Promotion of Science, Tokyo, Japan.

出版信息

Curr Protoc. 2025 Jan;5(1):e70075. doi: 10.1002/cpz1.70075.

Abstract

Arabidopsis thaliana, particularly the ecotype Columbia-0 (Col-0), has been extensively employed in the study of genetics of the nuclear genome. However, the difficulty of modifying the plastid genome of Col-0, the most widely used ecotype, has hindered investigation of the functional interactions between nuclear-encoded and plastid-encoded genes in this ecotype. Recently, we achieved targeted base editing, substituting a specific C:G pair with a T:A pair in the plastid genome of Col-0 through the application of genome-editing technology. This article introduces the method employed to accomplish this targeted base editing. The process involves four steps: (i) designing and constructing a binary vector encoding the genome-editing enzyme, (ii) introducing the binary vector into the nuclear genome of Col-0 via floral dipping, (iii) identifying base-edited plants, and (iv) verifying inheritance of the edited base(s) by the next generation. © 2025 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Design and construction of a binary vector encoding ptpTALECD or ptpTALECD_v2 Basic Protocol 2: Agrobacterium-mediated introduction of a binary vector into the Arabidopsis nuclear genome Basic Protocol 3: Selection of plants harboring T-DNA in the nucleus and detection of base editing in the plastid genome.

摘要

拟南芥,特别是生态型哥伦比亚-0(Col-0),已被广泛用于核基因组遗传学研究。然而,最广泛使用的生态型Col-0的质体基因组修饰困难,阻碍了对该生态型中核编码基因与质体编码基因之间功能相互作用的研究。最近,我们通过应用基因组编辑技术实现了靶向碱基编辑,在Col-0的质体基因组中将特定的C:G对替换为T:A对。本文介绍了实现这种靶向碱基编辑所采用的方法。该过程包括四个步骤:(i)设计和构建编码基因组编辑酶的二元载体,(ii)通过花浸法将二元载体导入Col-0的核基因组,(iii)鉴定碱基编辑的植物,以及(iv)验证下一代对编辑碱基的遗传。© 2025作者。由Wiley Periodicals LLC出版的《当前实验方案》。基本方案1:编码ptpTALECD或ptpTALECD_v2的二元载体的设计和构建 基本方案2:农杆菌介导的二元载体导入拟南芥核基因组 基本方案3:选择细胞核中含有T-DNA的植物并检测质体基因组中的碱基编辑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/188a/11701795/a49af737b389/CPZ1-5-0-g005.jpg

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