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Systems-level approaches for identifying and analyzing genetic interaction networks in Escherichia coli and extensions to other prokaryotes

机译:用于识别和分析大肠杆菌中的遗传相互作用网络以及扩展至其他原核生物的系统级方法

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摘要

Molecular interactions define the functional organization of the cell. Epistatic (genetic, or gene-gene) interactions, one of the most informative and commonly encountered forms of functional relationships, are increasingly being used to map process architecture in model eukaryotic organisms. In particular, 'systems-level' screens in yeast and worm aimed at elucidating genetic interaction networks have led to the generation of models describing the global modular organization of gene products and protein complexes within a cell. However, comparable data for prokaryotic organisms have not been available. Given its ease of growth and genetic manipulation, the Gram-negative bacterium Escherichia coli appears to be an ideal model system for performing comprehensive genome-scale examinations of genetic redundancy in bacteria. In this review, we highlight emerging experimental and computational techniques that have been developed recently to examine functional relationships and redundancy in E. coli at a systems-level, and their potential application to prokaryotes in general. Additionally, we have scanned PubMed abstracts and full-text published articles to manually curate a list of ~200 previously reported synthetic sick or lethal genetic interactions in E. coli derived from small-scale experimental studies.
机译:分子相互作用定义了细胞的功能组织。上位性(基因或基因-基因)相互作用是功能性关系中信息最丰富,最常遇到的形式之一,越来越多地用于绘制模型真核生物中的过程结构。尤其是,旨在阐明遗传相互作用网络的酵母和蠕虫的“系统级”筛选已导致描述描述细胞内基因产物和蛋白质复合物的全球模块化组织的模型的产生。但是,还没有可比较的原核生物数据。鉴于其易于生长和遗传操作,革兰氏阴性细菌似乎是进行细菌遗传冗余的全面基因组规模检查的理想模型系统。在这篇综述中,我们重点介绍了最近发展起来的新兴实验和计算技术,这些技术可以在系统级别上检查大肠杆菌中的功能关系和冗余性,以及它们在一般原核生物中的潜在应用。此外,我们还扫描了PubMed的摘要和全文发表的文章,以手动整理从小型实验研究中得出的大约200种先前报道的大肠杆菌中有病或致命遗传相互作用的列表。

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  • 来源
    《Molecular BioSystems》 |2009年第12期|1439-1455|共17页
  • 作者单位

    Banting and Best Department of Medical Research, Terrence Donnelly Center for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada M5S 3E1;

    Banting and Best Department of Medical Research, Terrence Donnelly Center for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada M5S 3E1;

    Banting and Best Department of Medical Research, Terrence Donnelly Center for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada M5S 3E1 Department of Biology, Wtldfrid Laurier University, Waterloo, Ontario, Canada N2L 3C5;

    Life Science Division, Lawrence Berkeley National Laboratory, Berkeley, USA CA 94720;

    Banting and Best Department of Medical Research, Terrence Donnelly Center for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada M5S 3E1;

    Banting and Best Department of Medical Research, Terrence Donnelly Center for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada M5S 3E1;

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