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基于系统发生的 DNA 微阵列的交叉杂交模型增加了对密切相关物种的检测能力。

Modelling cross-hybridization on phylogenetic DNA microarrays increases the detection power of closely related species.

机构信息

Department of Bioinformatics, Biocentre, University of Würzburg, Am Hubland, D-97074 Würzburg, Germany.

出版信息

Mol Ecol Resour. 2009 Jan;9(1):83-93. doi: 10.1111/j.1755-0998.2008.02199.x. Epub 2008 Oct 6.

DOI:10.1111/j.1755-0998.2008.02199.x
PMID:21564570
Abstract

DNA microarrays are a popular technique for the detection of microorganisms. Several approaches using specific oligomers targeting one or a few marker genes for each species have been proposed. Data analysis is usually limited to call a species present when its oligomer exceeds a certain intensity threshold. While this strategy works reasonably well for distantly related species, it does not work well for very closely related species: Cross-hybridization of nontarget DNA prevents a simple identification based on signal intensity. The majority of species of the same genus has a sequence similarity of over 90%. For biodiversity studies down to the species level, it is therefore important to increase the detection power of closely related species. We propose a simple, cost-effective and robust approach for biodiversity studies using DNA microarray technology and demonstrate it on scenedesmacean green algae. The internal transcribed spacer 2 (ITS2) rDNA sequence was chosen as marker because it is suitable to distinguish all eukaryotic species even though parts of it are virtually identical in closely related species. We show that by modelling hybridization behaviour with a matrix algebra approach, we are able to identify closely related species that cannot be distinguished with a threshold on signal intensity. Thus this proof-of-concept study shows that by adding a simple and robust data analysis step to the evaluation of DNA microarrays, species detection can be significantly improved for closely related species with a high sequence similarity.

摘要

DNA 微阵列是一种用于检测微生物的流行技术。已经提出了几种使用针对每个物种的一个或几个标记基因的特定寡聚物的方法。数据分析通常仅限于在其寡聚物超过某个强度阈值时调用存在的物种。虽然这种策略对于远缘物种的效果相当好,但对于非常近缘的物种效果不佳:非靶 DNA 的交叉杂交阻止了基于信号强度的简单识别。同一属的大多数物种的序列相似度超过 90%。对于种水平的生物多样性研究,因此,提高对近缘物种的检测能力非常重要。我们提出了一种简单、经济高效且稳健的方法,用于使用 DNA 微阵列技术进行生物多样性研究,并在 scenedesmacean 绿藻上进行了演示。内部转录间隔区 2(ITS2)rDNA 序列被选为标记物,因为它适合区分所有真核物种,即使在近缘物种中它的某些部分几乎相同。我们表明,通过使用矩阵代数方法模拟杂交行为,我们能够识别不能通过信号强度阈值区分的近缘物种。因此,这项概念验证研究表明,通过在 DNA 微阵列的评估中添加一个简单而稳健的数据分析步骤,可以显著提高具有高序列相似度的近缘物种的物种检测能力。

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