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使用 PowerSeq™ AUTO/Y 系统对南里奥格兰德州个体进行短串联重复序列的遗传分析。

Genetic analysis of Southern Brazil subjects using the PowerSeq™ AUTO/Y system for short tandem repeat sequencing.

机构信息

Molecular Biomedical Sciences, North Carolina State University, 1060 William Moore Dr., Raleigh, NC, 27607, USA; Forensic Sciences Institute, North Carolina State University, 1060 William Moore Dr., Raleigh, NC, 27607, USA.

Laboratory of Human and Molecular Genetics, Pontificia Universidade Catolica do Rio Grande do Sul,Av. Ipiranga 6681, Porto Alegre, RS, 90619-900, Brazil.

出版信息

Forensic Sci Int Genet. 2018 Mar;33:129-135. doi: 10.1016/j.fsigen.2017.12.008. Epub 2017 Dec 16.

Abstract

With the advent of Next-Generation Sequencing technology, sequencing of short tandem repeats (STRs) allows for a more detailed analysis when compared to size-based fragment methods (capillary electrophoresis-CE). The implementation of high-throughput sequencing can help uncover deeper genetic diversities of different populations. Subjects from the South region of Brazil present a particular and more homogeneous ancestry background when compared to other regions of the country. Both autosomal and Y- STRs have been analyzed in these individuals; however, all analyses published to date encompass data from CE-based fragment analysis. In this study, a genetic analysis of 59 individuals from Southern Brazil was performed on STR sequences. Forensically relevant STRs were PCR-enriched using a prototype of the PowerSeq™ AUTO/Y system (Promega Corp.). Next-generation sequencing was performed on an Illumina MiSeq instrument. The raw data (FASTQ files) were processed using a custom designed sequence processing tool, Altius. Isoalleles, which are sequence-based allelic variants that do not differ in length, were observed in nine autosomal and in six Y- STRs from the core global forensic marker set. The number of distinctive alleles based on sequence was higher when compared to those based on length, 37.3% higher in autosomal STRs and 13.8% higher in Y-STRs. The most polymorphic autosomal locus was D12S391, which presented 38 different sequence-based alleles. Among the loci in the Y chromosome, DYS389II presented the highest number of isoalleles. In comparison to CE analysis, Observed and Expected Heterozygosity, Polymorphic Information Content (PIC) and Genetic Diversity also presented higher values when the alleles were analyzed based on their sequence. For autosomal loci, Polymorphic Information Content (PIC) was 2.6% higher for sequence-based data. Diversity was 9.3% and 6.5% higher for autosomal and Y markers, respectively. In the analysis of the repeat structures for the STR loci, a new allele variant was found for allele 18 in the vWA locus. The STR flanking regions were also further investigated and sixteen variations were observed at nine autosomal STR loci and one Y-STR locus. The results obtained in this study demonstrate the importance of genetic analysis based on sequencing and highlight the diversity of the South Brazilian population when characterized by STR sequencing.

摘要

随着新一代测序技术的出现,与基于大小的片段方法(毛细管电泳-CE)相比,短串联重复序列(STRs)的测序可以进行更详细的分析。高通量测序的实施可以帮助揭示不同人群更深层次的遗传多样性。与该国其他地区相比,来自巴西南部地区的受试者具有特定且更加同质的祖先背景。这些个体的常染色体和 Y-STR 都已进行了分析;然而,迄今为止所有已发表的分析都涵盖了基于 CE 的片段分析的数据。在这项研究中,对来自巴西南部的 59 个人进行了 STR 序列的遗传分析。使用 PowerSeq™ AUTO/Y 系统(Promega Corp.)的原型对法医相关 STR 进行了 PCR 富集。在 Illumina MiSeq 仪器上进行了下一代测序。使用自定义设计的序列处理工具 Altius 处理原始数据(FASTQ 文件)。在核心全球法医标记集中,在九个常染色体和六个 Y-STR 中观察到了基于序列的等位基因变异体,这些等位基因变异体在长度上没有差异。基于序列的独特等位基因数量高于基于长度的独特等位基因数量,常染色体 STR 高 37.3%,Y-STR 高 13.8%。最具多态性的常染色体基因座是 D12S391,它有 38 个不同的基于序列的等位基因。在 Y 染色体上的基因座中,DYS389II 具有最高数量的同工等位基因。与 CE 分析相比,当根据序列分析等位基因时,观察到的和预期的杂合度、多态信息含量(PIC)和遗传多样性也呈现出更高的值。对于常染色体基因座,基于序列的数据的多态信息含量(PIC)高 2.6%。多态性分别高出 9.3%和 6.5%,用于常染色体和 Y 标记。在 STR 基因座重复结构的分析中,在 vWA 基因座中发现了等位基因 18 的新等位基因变异体。还进一步研究了 STR 侧翼区域,在九个常染色体 STR 基因座和一个 Y-STR 基因座观察到 16 种变异。本研究的结果表明了基于测序的遗传分析的重要性,并突出了 STR 测序时巴西南部人群的多样性。

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