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Development of an Environmental Functional Gene Microarray for Soil Microbial Communities

机译:土壤微生物群落环境功能基因芯片的开发

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摘要

Functional attributes of microbial communities are difficult to study, and most current techniques rely on DNA- and rRNA-based profiling of taxa and genes, including microarrays containing sequences of known microorganisms. To quantify gene expression in environmental samples in a culture-independent manner, we constructed an environmental functional gene microarray (E-FGA) consisting of 13,056 mRNA-enriched anonymous microbial clones from diverse microbial communities to profile microbial gene transcripts. A new normalization method using internal spot standards was devised to overcome spotting and hybridization bias, enabling direct comparisons of microarrays. To evaluate potential applications of this metatranscriptomic approach for studying microbes in environmental samples, we tested the E-FGA by profiling the microbial activity of agricultural soils with a low or high flux of N2O. A total of 109 genes displayed expression that differed significantly between soils with low and high N2O emissions. We conclude that mRNA-based approaches such as the one presented here may complement existing techniques for assessing functional attributes of microbial communities.
机译:微生物群落的功能属性很难研究,并且大多数当前技术依赖于基于DNA和rRNA的分类单元和基因谱分析,包括含有已知微生物序列的微阵列。为了以独立于培养的方式量化环境样品中的基因表达,我们构建了一个环境功能基因微阵列(E-FGA),该阵列由来自各种微生物群落的富含1,056 mRNA的匿名微生物克隆组成,以分析微生物基因转录本。设计了一种使用内部斑点标准的新归一化方法,以克服斑点和杂交偏差,从而可以直接比较微阵列。为了评估这种超转录组学方法在研究环境样品中微生物的潜在应用,我们通过分析低或高N2O通量的农业土壤的微生物活性来测试E-FGA。总共109个基因显示出的表达在低和高N2O排放的土壤之间存在显着差异。我们得出结论,基于mRNA的方法(如此处介绍的方法)可能会补充现有的评估微生物群落功能属性的技术。

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