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转座子辅助基因插入技术(TAGIT):一种用于生成荧光融合蛋白的工具。

Transposon assisted gene insertion technology (TAGIT): a tool for generating fluorescent fusion proteins.

机构信息

Division of Biological Sciences, University of California San Diego, La Jolla, California, United States of America.

出版信息

PLoS One. 2010 Jan 15;5(1):e8731. doi: 10.1371/journal.pone.0008731.

Abstract

We constructed a transposon (transposon assisted gene insertion technology, or TAGIT) that allows the random insertion of gfp (or other genes) into chromosomal loci without disrupting operon structure or regulation. TAGIT is a modified Tn5 transposon that uses Kan(R) to select for insertions on the chromosome or plasmid, beta-galactosidase to identify in-frame gene fusions, and Cre recombinase to excise the kan and lacZ genes in vivo. The resulting gfp insertions maintain target gene reading frame (to the 5' and 3' of gfp) and are integrated at the native chromosomal locus, thereby maintaining native expression signals. Libraries can be screened to identify GFP insertions that maintain target protein function at native expression levels, allowing more trustworthy localization studies. We here use TAGIT to generate a library of GFP insertions in the Escherichia coli lactose repressor (LacI). We identified fully functional GFP insertions and partially functional insertions that bind DNA but fail to repress the lacZ operon. Several of these latter GFP insertions localize to lacO arrays integrated in the E. coli chromosome without producing the elongated cells frequently observed when functional LacI-GFP fusions are used in chromosome tagging experiments. TAGIT thereby faciliates the isolation of fully functional insertions of fluorescent proteins into target proteins expressed from the native chromosomal locus as well as potentially useful partially functional proteins.

摘要

我们构建了一个转座子(转座子辅助基因插入技术,或 TAGIT),它允许 GFP(或其他基因)随机插入染色体基因座,而不会破坏操纵子结构或调控。TAGIT 是一种改良的 Tn5 转座子,它使用 Kan(R)选择在染色体或质粒上进行插入,使用β-半乳糖苷酶鉴定框内基因融合,使用 Cre 重组酶在体内切除 kan 和 lacZ 基因。由此产生的 GFP 插入物保持靶基因的阅读框(到 GFP 的 5'和 3'),并整合到天然染色体基因座上,从而保持天然表达信号。可以对文库进行筛选,以鉴定在天然表达水平下保持靶蛋白功能的 GFP 插入物,从而进行更可靠的定位研究。我们在这里使用 TAGIT 在大肠杆菌乳糖阻遏物(LacI)中生成 GFP 插入物文库。我们鉴定了完全功能的 GFP 插入物和部分功能的插入物,这些插入物结合 DNA,但不能抑制 lacZ 操纵子。这些 GFP 插入物中的几个定位于整合在大肠杆菌染色体上的 lacO 阵列,而不会在使用功能 LacI-GFP 融合进行染色体标记实验时经常观察到伸长的细胞。因此,TAGIT 促进了荧光蛋白完全功能的插入物在天然染色体基因座表达的靶蛋白中的分离,以及可能有用的部分功能蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93f1/2806921/b4b94ab84908/pone.0008731.g001.jpg

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