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首页> 外文期刊>Applied and Environmental Microbiology >Diversity and depth-specific distribution of SAR11 cluster rRNA genes from marine planktonic bacteria.
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Diversity and depth-specific distribution of SAR11 cluster rRNA genes from marine planktonic bacteria.

机译:来自海洋浮游细菌的SAR11簇rRNA基因的多样性和深度特异性分布。

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摘要

Small-subunit (SSU) ribosomal DNA (rDNA) gene clusters are phylogenetically related sets of SSU rRNA genes, commonly encountered in genes amplified from natural populations. Genetic variability in gene clusters could result from artifacts (polymerase error or PCR chimera formation), microevolution (variation among rrn copies within strains), or macroevolution (genetic divergence correlated with long-term evolutionary divergence). To better understand gene clusters this study assessed genetic diversity and distribution of a single environmental SSU rDNA gene cluster, the SAR11 cluster. SAR11 cluster genes, from an uncultured group of the alpha subclass of the class Proteobacteria, have been recovered from coastal and midoceanic waters of the North Atlantic and Pacific. We cloned and bidirectionally sequenced 23 new SAR11 cluster 16S rRNA genes, from 80 and 250 m in the Sargasso Sea and from surface coastal waters of the Atlantic and Pacific, and analyzed them with previously published sequences. Two SAR11 genes were obviously PCR chimeras, but the biological (nonchimeric) origins of most subgroups within the cluster were confirmed by independent recovery from separate gene libraries. Using group-specific oligonucleotide probes, we analyzed depth profiles of nucleic acids, targeting both amplified rDNAs and bulk RNAs. Two subgroups within the SAR11 cluster showed different highly depth-specific distributions. We conclude that some of the genetic diversity within the SAR11 gene cluster represents macroevolutionary divergence correlated with niche specialization. Furthermore, we demonstrate the utility for marine microbial ecology of oligonucleotide probes based on gene sequences amplified from natural populations and show that a detailed knowledge of sequence variability may be needed to effectively design these probes.
机译:小亚基(SSU)核糖体DNA(rDNA)基因簇是系统发育相关的SSU rRNA基因集,通常在从自然种群扩增的基因中遇到。基因簇中的遗传变异性可能是由人工产物(聚合酶错误或PCR嵌合体形成),微观进化(菌株内rrn拷贝之间的变异)或宏观进化(遗传差异与长期进化差异相关)造成的。为了更好地了解基因簇,本研究评估了单个环境SSU rDNA基因簇SAR11簇的遗传多样性和分布。 SAR11簇基因来自Proteobacteria类的一个非养殖α亚类群,已从北大西洋和太平洋的沿海和中洋水域中回收。我们从Sargasso海的80和250 m以及大西洋和太平洋的表层沿海水域克隆了23个新的SAR11簇16S rRNA基因并对其进行了双向测序,并使用以前发表的序列对其进行了分析。两个SAR11基因显然是PCR嵌合体,但是簇中大多数亚组的生物学(非嵌合)起源是通过从单独的基因库中独立回收得到的。使用特定于组的寡核苷酸探针,我们分析了针对扩增的rDNA和大量RNA的核酸深度概况。 SAR11集群中的两个子组显示出不同的高度特定深度分布。我们得出的结论是,SAR11基因簇内的某些遗传多样性代表了与生态位特化相关的宏观进化差异。此外,我们展示了基于从自然种群中扩增的基因序列的寡核苷酸探针在海洋微生物生态学中的实用性,并表明可能需要序列变异的详细知识才能有效地设计这些探针。

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