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噬菌体 phiC31 整合酶介导的小麦染色体中转基因的切除。

Transgene excision from wheat chromosomes by phage phiC31 integrase.

机构信息

Leibniz-Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK) Gatersleben, Corrensstr. 3, 06466, Gatersleben, Germany.

出版信息

Plant Mol Biol. 2010 Apr;72(6):673-87. doi: 10.1007/s11103-010-9606-7. Epub 2010 Feb 2.

Abstract

The Streptomyces phage phiC31 integrase was tested for its ability to excise transgenic DNA from the wheat genome by site-specific recombination. Plants that stably express phiC31 integrase were crossed to plants carrying a target construct bearing the phiC31 recognition sites, attP and attB. In the progeny, phiC31 recombinase mediates recombination between the att sites of the target locus, which results in excision of the intervening DNA. Recombination events could be identified in 34 independent wheat lines by PCR and Southern blot analysis and by sequencing of the excision footprints. Recombinant loci were inherited to the subsequent generation. The results presented here establish the integrase-att system as a tool for catalysing the precise elimination of DNA sequences from wheat chromosomes.

摘要

链霉菌噬菌体 phiC31 整合酶被测试其通过位点特异性重组从小麦基因组中切除转基因 DNA 的能力。稳定表达 phiC31 整合酶的植物与携带带有 phiC31 识别位点 attP 和 attB 的靶标构建体的植物杂交。在后代中,phiC31 重组酶介导靶标基因座 att 位点之间的重组,导致中间 DNA 的切除。通过 PCR 和 Southern 印迹分析以及切除足迹的测序,在 34 个独立的小麦株系中可鉴定重组事件。重组基因座被遗传到后续的世代。这里呈现的结果确立了整合酶-att 系统作为催化从小麦染色体中精确消除 DNA 序列的工具。

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