首页> 美国卫生研究院文献>DNA Research: An International Journal for Rapid Publication of Reports on Genes and Genomes >Construction of Signature-tagged Mutant Library in Mesorhizobium loti as a Powerful Tool for Functional Genomics
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Construction of Signature-tagged Mutant Library in Mesorhizobium loti as a Powerful Tool for Functional Genomics

机译:作为功​​能基因组学的强大工具在水生中生根瘤菌中标记标签的突变体文库的构建

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摘要

Rhizobia are nitrogen-fixing soil bacteria that establish endosymbiosis with some leguminous plants. The completion of several rhizobial genome sequences provides opportunities for genome-wide functional studies of the physiological roles of many rhizobial genes. In order to carry out genome-wide phenotypic screenings, we have constructed a large mutant library of the nitrogen-fixing symbiotic bacterium, Mesorhizobium loti, by transposon mutagenesis. Transposon insertion mutants were generated using the signature-tagged mutagenesis (STM) technique and a total of 29 330 independent mutants were obtained. Along with the collection of transposon mutants, we have determined the transposon insertion sites for 7892 clones, and confirmed insertions in 3680 non-redundant M. loti genes (50.5% of the total number of M. loti genes). Transposon insertions were randomly distributed throughout the M. loti genome without any bias toward G+C contents of insertion target sites and transposon plasmids used for the mutagenesis. We also show the utility of STM mutants by examining the specificity of signature tags and test screenings for growth- and nodulation-deficient mutants. This defined mutant library allows for genome-wide forward- and reverse-genetic functional studies of M. loti and will serve as an invaluable resource for researchers to further our understanding of rhizobial biology.
机译:根瘤菌是固氮土壤细菌,可与某些豆科植物建立共生关系。几个根瘤菌基因组序列的完成为许多根瘤菌基因的生理作用提供了全基因组功能研究的机会。为了进行全基因组的表型筛选,我们通过转座子诱变构建了一个固氮共生细菌Lot mezohizobium loti的大型突变体文库。使用签名标记诱变(STM)技术生成转座子插入突变体,并获得了总共29 330个独立突变体。连同转座子突变体的收集,我们已经确定了7892个克隆的转座子插入位点,并确认了3680个非冗余的M. loti基因(占M. loti基因总数的50.5%)的插入。转座子插入随机分布在整个罗氏支原体基因组中,而对插入目标位点和用于诱变的转座子质粒的G + C含量没有任何偏见。我们还通过检查签名标签的特异性以及测试生长和结瘤缺陷型突变体的筛选来显示STM突变体的效用。这个定义的突变体文库可用于对Loti支原体进行全基因组的正向和反向基因功能研究,并将成为研究人员进一步了解根瘤菌生物学的宝贵资源。

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