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利用RecA-绿色荧光蛋白对大肠杆菌K-12中的RecA进行定位

Localization of RecA in Escherichia coli K-12 using RecA-GFP.

作者信息

Renzette Nicholas, Gumlaw Nathan, Nordman Jared T, Krieger Marlee, Yeh Su-Ping, Long Edward, Centore Richard, Boonsombat Ruethairat, Sandler Steven J

机构信息

Molecular and Cellular Biology Graduate Program, University of Massachusetts, Amherst, MA 01003, USA.

出版信息

Mol Microbiol. 2005 Aug;57(4):1074-85. doi: 10.1111/j.1365-2958.2005.04755.x.

Abstract

RecA is important in recombination, DNA repair and repair of replication forks. It functions through the production of a protein-DNA filament. To study the localization of RecA in live Escherichia coli cells, the RecA protein was fused to the green fluorescence protein (GFP). Strains with this gene have recombination/DNA repair activities three- to tenfold below wild type (or about 1000-fold above that of a recA null mutant). RecA-GFP cells have a background of green fluorescence punctuated with up to five foci per cell. Two types of foci have been defined: 4,6-diamidino-2-phenylindole (DAPI)-sensitive foci that are bound to DNA and DAPI-insensitive foci that are DNA-less aggregates/storage structures. In log phase cells, foci were not localized to any particular region. After UV irradiation, the number of foci increased and they localized to the cell centre. This suggested colocalization with the DNA replication factory. recA, recB and recF strains showed phenotypes and distributions of foci consistent with the predicted effects of these mutations.

摘要

RecA在重组、DNA修复及复制叉修复过程中发挥重要作用。它通过形成蛋白质-DNA细丝发挥功能。为研究RecA在活的大肠杆菌细胞中的定位,将RecA蛋白与绿色荧光蛋白(GFP)融合。含有该基因的菌株其重组/DNA修复活性比野生型低三到十倍(或比recA基因敲除突变体高约1000倍)。RecA-GFP细胞具有绿色荧光背景,每个细胞中有多达五个荧光焦点。已定义了两种类型的焦点:与DNA结合的4,6-二脒基-2-苯基吲哚(DAPI)敏感焦点和无DNA的聚集体/储存结构的DAPI不敏感焦点。在对数期细胞中,焦点不定位于任何特定区域。紫外线照射后,焦点数量增加并定位于细胞中心。这表明与DNA复制工厂共定位。recA、recB和recF菌株显示出与这些突变的预测效应一致的焦点表型和分布。

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