Sequencing the orthologs of human autosomal forensic short tandem repeats provides individual- and species-level identification in African great apes.

IF 2.3 Q2 ECOLOGY
Ettore Fedele, Jon H Wetton, Mark A Jobling
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Abstract

Background: Great apes are a global conservation concern, with anthropogenic pressures threatening their survival. Genetic analysis can be used to assess the effects of reduced population sizes and the effectiveness of conservation measures. In humans, autosomal short tandem repeats (aSTRs) are widely used in population genetics and for forensic individual identification and kinship testing. Traditionally, genotyping is length-based via capillary electrophoresis (CE), but there is an increasing move to direct analysis by massively parallel sequencing (MPS). An example is the ForenSeq DNA Signature Prep Kit, which amplifies multiple loci including 27 aSTRs, prior to sequencing via Illumina technology. Here we assess the applicability of this human-based kit in African great apes. We ask whether cross-species genotyping of the orthologs of these loci can provide both individual and (sub)species identification.

Results: The ForenSeq kit was used to amplify and sequence aSTRs in 52 individuals (14 chimpanzees; 4 bonobos; 16 western lowland, 6 eastern lowland, and 12 mountain gorillas). The orthologs of 24/27 human aSTRs amplified across species, and a core set of thirteen loci could be genotyped in all individuals. Genotypes were individually and (sub)species identifying. Both allelic diversity and the power to discriminate (sub)species were greater when considering STR sequences rather than allele lengths. Comparing human and African great-ape STR sequences with an orangutan outgroup showed general conservation of repeat types and allele size ranges. Variation in repeat array structures and a weak relationship with the known phylogeny suggests stochastic origins of mutations giving rise to diverse imperfect repeat arrays. Interruptions within long repeat arrays in African great apes do not appear to reduce allelic diversity.

Conclusions: Orthologs of most human aSTRs in the ForenSeq DNA Signature Prep Kit can be analysed in African great apes. Primer redesign would reduce observed variability in amplification across some loci. MPS of the orthologs of human loci provides better resolution for both individual and (sub)species identification in great apes than standard CE-based approaches, and has the further advantage that there is no need to limit the number and size ranges of analysed loci.

对人类常染色体法医短串联重复序列的直向同源物进行测序,可对非洲类人猿进行个体和物种级别的鉴定。
背景:类人猿是全球关注的保护对象,其生存受到人为压力的威胁。遗传分析可用于评估种群数量减少的影响和保护措施的有效性。在人类中,常染色体短串联重复序列(aSTR)被广泛用于群体遗传学、法医个体鉴定和亲属关系测试。传统上,基因分型是通过毛细管电泳(CE)进行长度分析,但现在越来越多地采用大规模并行测序(MPS)进行直接分析。ForenSeq DNA Signature Prep Kit 就是一个例子,它能在通过 Illumina 技术测序之前扩增多个位点,包括 27 个 aSTR。在这里,我们评估了这种基于人类的试剂盒在非洲类人猿中的适用性。我们想知道对这些基因座的直向同源物进行跨物种基因分型是否能提供个体和(亚)物种鉴定:结果:使用 ForenSeq 试剂盒对 52 个个体(14 只黑猩猩、4 只倭黑猩猩、16 只西部低地大猩猩、6 只东部低地大猩猩和 12 只山地大猩猩)的 aSTRs 进行了扩增和测序。24/27 个人类 aSTRs 的直向同源物在不同物种间进行了扩增,13 个核心位点可在所有个体中进行基因分型。基因型可进行个体和(亚)物种鉴定。当考虑 STR 序列而不是等位基因长度时,等位基因多样性和区分(亚)物种的能力都更强。将人类和非洲巨猿的 STR 序列与猩猩外群进行比较,结果显示重复类型和等位基因大小范围基本一致。重复序列结构的差异以及与已知系统发育的微弱关系表明,突变的随机起源导致了各种不完善的重复序列。非洲类人猿长重复序列的中断似乎并没有减少等位基因的多样性:结论:ForenSeq DNA Signature Prep Kit 中大多数人类 aSTR 的同源物可在非洲类人猿中进行分析。引物的重新设计将减少在某些位点上观察到的扩增变异。与基于标准CE的方法相比,人类基因座直向同源物的MPS在类人猿的个体和(亚)物种鉴定方面具有更高的分辨率,而且还具有无需限制所分析基因座的数量和大小范围的优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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