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Intragenomic Profiling Using Multicopy Genes: The rDNA Internal Transcribed Spacer Sequences of the Freshwater Sponge Ephydatia fluviatilis

机译:使用多拷贝基因的Intragenomic分析:淡水海绵埃弗氏菌的rDNA内部转录的间隔序列。

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摘要

Multicopy genes, like ribosomal RNA genes (rDNA), are widely used to describe and distinguish individuals. Despite concerted evolution that homogenizes a large number of rDNA gene copies, the presence of different gene variants within a genome has been reported. Characterization of an organism by defining every single variant of tens to thousands of rDNA repeat units present in a eukaryotic genome would be quite unreasonable. Here we provide an alternative approach for the characterization of a set of internal transcribed spacer sequences found within every rDNA repeat unit by implementing direct sequencing methodology. The prominent allelic variants and their relative amounts characterizing an individual can be described by a single sequencing electropherogram of the mixed amplicon containing the variants present within the genome. We propose a method for rational analysis of heterogeneity of multicopy genes by compiling a profile based on quantification of different sequence variants of the internal transcribed spacers of the freshwater sponge Ephydatia fluviatilis as an example. In addition to using conventional substitution analysis, we have developed a mathematical method, the proportion model method, to quantify the relative amounts of allelic variants of different length using data from direct sequencing of the heterogeneous amplicon. This method is based on determining the expected signal intensity values (corresponding to peak heights from the sequencing electropherogram) by sequencing clones from the same or highly similar amplicon and comparing hypothesized combinations against the values obtained by direct sequencing of the heterogeneous amplicon. This method allowed to differentiate between all specimens analysed.
机译:像核糖体RNA基因(rDNA)一样,多拷贝基因被广泛用于描述和区分个体。尽管协调一致的进化使大量的rDNA基因拷贝均质化,但是已经报道了基因组内不同基因变体的存在。通过定义真核生物基因组中存在的数十至数千个rDNA重复单元的每个单个变体来表征生物体是非常不合理的。在这里,我们通过实施直接测序方法,为表征在每个rDNA重复单元中发现的一组内部转录间隔子序列提供了另一种方法。可以通过包含基因组内存在的变异体的混合扩增子的单次测序电泳图谱来描述表征个体的突出的等位基因变异体及其相对量。我们提出了一种通过对基于淡水海绵埃弗氏菌(Ephydatia fluviatilis)内部转录间隔区的不同序列变异体进行定量分析的谱图来合理分析多拷贝基因异质性的方法。除了使用常规的替代分析外,我们还开发了一种数学方法,即比例模型方法,使用来自异源扩增子的直接测序数据来量化不同长度的等位基因变体的相对数量。该方法的基础是通过对来自相同或高度相似的扩增子的克隆进行测序,并将假设的组合与通过异源扩增子的直接测序获得的值进行比较,确定预期的信号强度值(对应于测序电泳图的峰高)。这种方法可以区分所分析的所有标本。

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