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大肠杆菌K-12框内单基因敲除突变体的构建:Keio文库。

Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection.

作者信息

Baba Tomoya, Ara Takeshi, Hasegawa Miki, Takai Yuki, Okumura Yoshiko, Baba Miki, Datsenko Kirill A, Tomita Masaru, Wanner Barry L, Mori Hirotada

机构信息

Institute for Advanced Biosciences, Keio University, Tsuruoka City, Yamagata, Japan.

出版信息

Mol Syst Biol. 2006;2:2006.0008. doi: 10.1038/msb4100050. Epub 2006 Feb 21.

Abstract

We have systematically made a set of precisely defined, single-gene deletions of all nonessential genes in Escherichia coli K-12. Open-reading frame coding regions were replaced with a kanamycin cassette flanked by FLP recognition target sites by using a one-step method for inactivation of chromosomal genes and primers designed to create in-frame deletions upon excision of the resistance cassette. Of 4288 genes targeted, mutants were obtained for 3985. To alleviate problems encountered in high-throughput studies, two independent mutants were saved for every deleted gene. These mutants-the 'Keio collection'-provide a new resource not only for systematic analyses of unknown gene functions and gene regulatory networks but also for genome-wide testing of mutational effects in a common strain background, E. coli K-12 BW25113. We were unable to disrupt 303 genes, including 37 of unknown function, which are candidates for essential genes. Distribution is being handled via GenoBase (http://ecoli.aist-nara.ac.jp/).

摘要

我们系统地构建了一组对大肠杆菌K-12中所有非必需基因进行精确定义的单基因缺失突变体。通过使用一种一步法使染色体基因失活,并设计引物以便在切除抗性盒后产生框内缺失,将开放阅读框编码区域替换为两侧带有FLP识别靶点的卡那霉素盒。在4288个靶向基因中,获得了3985个基因的突变体。为了缓解高通量研究中遇到的问题,每个缺失基因保存了两个独立的突变体。这些突变体——“Keio文库”——不仅为未知基因功能和基因调控网络的系统分析提供了新资源,也为在常见菌株背景大肠杆菌K-12 BW25113中进行全基因组突变效应测试提供了新资源。我们无法破坏303个基因,包括37个功能未知的基因,这些基因是必需基因的候选者。相关信息正在通过GenoBase(http://ecoli.aist-nara.ac.jp/)进行处理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a03c/1681482/cb779c2cae86/msb4100050-f1.jpg

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