A systematic search for discriminating sites in the 16S ribosomal RNA gene.

Hilde Vinje, Trygve Almøy, Kristian Hovde Liland, Lars Snipen
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引用次数: 21

Abstract

Background: The 16S rRNA is by far the most common genomic marker used for prokaryotic classification, and has been used extensively in metagenomic studies over recent years. Along the 16S gene there are regions with more or less variation across the kingdom of bacteria. Nine variable regions have been identified, flanked by more conserved parts of the sequence. It has been stated that the discriminatory power of the 16S marker lies in these variable regions. In the present study we wanted to examine this more closely, and used a supervised learning method to search systematically for sites that contribute to correct classification at either the phylum or genus level.

Results: When classifying phyla the site selection algorithm located 50 discriminative sites. These were scattered over most of the alignments and only around half of them were located in the variable regions. The selected sites did, however, have an entropy significantly larger than expected, meaning they are sites of large variation. We found that the discriminative sites typically have a large entropy compared to their closest neighbours along the alignments. When classifying genera the site selection algorithm needed around 80% of the sites in the 16S gene before the classification error reached a minimum. This means that all variation, in both variable and conserved regions, is needed in order to separate genera.

Conclusions: Our findings does not support the statement that the discriminative power of the 16S gene is located only in the variable regions. Variable regions are important, but just as many discriminative sites are found in the more conserved parts. The discriminative power is typically found in sites of large variation located inside shorter regions of higher conservation.

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对16S核糖体RNA基因中区分位点的系统搜索。
背景:16S rRNA是迄今为止最常用的用于原核生物分类的基因组标记,近年来在宏基因组研究中被广泛使用。沿着16S基因,在细菌王国中有或多或少变异的区域。已经确定了九个可变区域,两侧是序列的更保守的部分。已经指出,16S标记的歧视性力量在于这些可变区域。在本研究中,我们想要更仔细地检查这一点,并使用监督学习方法系统地搜索有助于门或属水平正确分类的位点。结果:在分类门时,该算法确定了50个判别位点。它们分散在大多数排列中,只有大约一半位于可变区域。然而,所选地点的熵值明显大于预期,这意味着它们是变化很大的地点。我们发现,与沿着排列的最近邻居相比,鉴别位点通常具有较大的熵。在分类属时,位点选择算法需要约80%的16S基因位点才能使分类误差达到最小。这意味着所有的变异,无论是在可变区还是保守区,都是分离属所必需的。结论:我们的研究结果不支持16S基因的鉴别能力仅位于可变区域的说法。可变区域很重要,但在更保守的部分也发现了许多区别位点。鉴别力通常在位于较短的较高保守性区域内的大变异位点上发现。
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A systematic search for discriminating sites in the 16S ribosomal RNA gene. Deep sequencing of evolving pathogen populations: applications, errors, and bioinformatic solutions. Sialic acid utilization by Cronobacter sakazakii. Beginner's guide to comparative bacterial genome analysis using next-generation sequence data. An efficient rRNA removal method for RNA sequencing in GC-rich bacteria.
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