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Comparative Analysis of Eukaryotic Marine Microbial Assemblages from 18S rRNA Gene and Gene Transcript Clone Libraries by Using Different Methods of Extraction

机译:不同提取方法对18S rRNA基因和基因转录克隆文库真核生物海洋微生物的比较分析

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Eukaryotic marine microbes play pivotal roles in biogeochemical nutrient cycling and ecosystem function, but studies that focus on the protistan biogeography and genetic diversity lag-behind studies of other microbes. 18S rRNA PCR amplification and clone library sequencing are commonly used to assess diversity that is culture independent. However, molecular methods are not without potential biases and artifacts. In this study, we compare the community composition of clone libraries generated from the same water sample collected at the San Pedro Ocean Time Series (SPOTs) station in the northwest Pacific Ocean. Community composition was assessed using different cell lysis methods (chemical and mechanical) and the extraction of different nucleic acids (DNA and RNA reverse transcribed to cDNA) to build Sanger ABI clone libraries. We describe specific biases for ecologically important phylogenetic groups resulting from differences in nucleic acid extraction methods that will inform future designs of eukaryotic diversity studies, regardless of the target sequencing platform planned.
机译:真核海洋微生物在生物地球化学养分循环和生态系统功能中起着关键作用,但是专注于原生生物地理和遗传多样性的研究滞后于其他微生物。 18S rRNA PCR扩增和克隆文库测序通常用于评估与培养无关的多样性。但是,分子方法并非没有潜在的偏差和人为因素。在这项研究中,我们比较了从西北太平洋San Pedro海洋时间序列(SPOT)站收集的同一水样中生成的克隆文库的群落组成。使用不同的细胞裂解方法(化学和机械方法)和提取不同的核酸(DNA和RNA反转录为cDNA)评估群落组成,以构建Sanger ABI克隆文库。我们描述了由于核酸提取方法的差异而导致的具有生态学意义的重要系统发育群体的具体偏见,无论拟定的靶标测序平台如何,这将为将来的真核生物多样性研究提供参考。

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