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Ti 质粒载体可将 DNA 导入植物细胞而不改变其正常的再生能力。

Ti plasmid vector for the introduction of DNA into plant cells without alteration of their normal regeneration capacity.

机构信息

Laboratorium voor Genetica, Rijksuniversiteit Gent, B-9000 Gent, Belgium.

出版信息

EMBO J. 1983;2(12):2143-50. doi: 10.1002/j.1460-2075.1983.tb01715.x.

DOI:10.1002/j.1460-2075.1983.tb01715.x
PMID:16453482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC555426/
Abstract

A Ti plasmid mutant was constructed in which all the on-cogenic functions of the T-DNA have been deleted and replaced by pBR322. This Ti plasmid, pGV3850, still mediates efficient transfer and stabilization of its truncated T-DNA into infected plant cells. Moreover, integration and expression of this minimal T-DNA in plant cells does not interfere with normal plant cell differentiation. A DNA fragment cloned in a pBR vector can be inserted in the pGV3850 T-region upon a single recombination event through the pBR322 region of pGV3850 producing a co-integrate useful for the transformation of plant cells. Based upon these properties, pGV3850 is proposed as an extremely versatile vector for the introduction of any DNA of interest into plant cells.

摘要

构建了一个 Ti 质粒突变体,其中 T-DNA 的所有致癌功能已被删除,并被 pBR322 取代。这种 Ti 质粒,pGV3850,仍然介导其截断的 T-DNA 有效转移和稳定到感染的植物细胞中。此外,该最小 T-DNA 在植物细胞中的整合和表达不会干扰正常的植物细胞分化。克隆在 pBR 载体中的 DNA 片段可以通过 pGV3850 的 pBR322 区域在单个重组事件中插入 pGV3850 的 T 区,产生一个用于植物细胞转化的共整合体。基于这些特性,pGV3850 被提议作为一种非常通用的载体,用于将任何感兴趣的 DNA 引入植物细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee2f/555426/2fd8eab5c026/emboj00265-0055-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee2f/555426/5932ad1a3b60/emboj00265-0053-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee2f/555426/2626ca3f74a8/emboj00265-0054-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee2f/555426/2fd8eab5c026/emboj00265-0055-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee2f/555426/5932ad1a3b60/emboj00265-0053-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee2f/555426/2626ca3f74a8/emboj00265-0054-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee2f/555426/2fd8eab5c026/emboj00265-0055-a.jpg

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Ti plasmid vector for the introduction of DNA into plant cells without alteration of their normal regeneration capacity.Ti 质粒载体可将 DNA 导入植物细胞而不改变其正常的再生能力。
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Short direct repeats flank the T-DNA on a nopaline Ti plasmid.短直接重复序列侧翼在胭脂碱 Ti 质粒上的 T-DNA。
Proc Natl Acad Sci U S A. 1982 Oct;79(20):6322-6. doi: 10.1073/pnas.79.20.6322.
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Recombination between higher plant DNA and the Ti plasmid of Agrobacterium tumefaciens.高等植物 DNA 与土壤杆菌 Ti 质粒的重组。
Proc Natl Acad Sci U S A. 1980 Nov;77(11):6448-52. doi: 10.1073/pnas.77.11.6448.
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Chimeric genes as dominant selectable markers in plant cells.嵌合基因作为植物细胞中的显性选择标记。
Microorganisms. 2024 Sep 30;12(10):1999. doi: 10.3390/microorganisms12101999.
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Exploring Agrobacterium-mediated genetic transformation methods and its applications in Lilium.探索农杆菌介导的遗传转化方法及其在百合中的应用。
Plant Methods. 2024 Aug 9;20(1):120. doi: 10.1186/s13007-024-01246-8.
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History and current status of embryogenic culture-based tissue culture, transformation and gene editing of maize (Zea mays L.).基于胚性培养的玉米(Zea mays L.)组织培养、转化及基因编辑的历史与现状
Plant Genome. 2025 Mar;18(1):e20451. doi: 10.1002/tpg2.20451. Epub 2024 Apr 11.
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A simple and efficient protocol for generating transgenic hairy roots using Agrobacterium rhizogenes.利用发根农杆菌高效生产转基因毛状根的简单方法。
PLoS One. 2023 Nov 1;18(11):e0291680. doi: 10.1371/journal.pone.0291680. eCollection 2023.
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Genomic consequences associated with Agrobacterium-mediated transformation of plants.与农杆菌介导的植物转化相关的基因组后果。
Plant J. 2024 Jan;117(2):342-363. doi: 10.1111/tpj.16496. Epub 2023 Oct 13.
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Agrobacterium tumefaciens: a Transformative Agent for Fundamental Insights into Host-Microbe Interactions, Genome Biology, Chemical Signaling, and Cell Biology.根瘤农杆菌:在宿主-微生物相互作用、化学信号转导和细胞生物学方面的基础见解的变革性因子。
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4
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6
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EMBO J. 1983;2(3):411-7. doi: 10.1002/j.1460-2075.1983.tb01438.x.
7
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