Boscari Elisa, Palle Stefano Dalle, Vitulo Nicola, Scapolatiello Annalisa, Schiavon Luca, Cariani Alessia, Papetti Chiara, Zane Lorenzo, Marino Ilaria Anna Maria, Congiu Leonardo
Department of Biology, University of Padova, Via Ugo Bassi 58B, 35121, Padova, Italy.
Department of Biotechnology, University of Verona, Strada le Grazie, 15, 37134, Verona, Italy.
Sci Rep. 2024 Aug 1;14(1):17870. doi: 10.1038/s41598-024-68065-8.
The study of species groups in which the presence of interspecific hybridization or introgression phenomena is known or suspected involves analysing shared bi-parentally inherited molecular markers. Current methods are based on different categories of markers among which the classical microsatellites or the more recent genome wide approaches for the analyses of thousands of SNPs or hundreds of microhaplotypes through high throughput sequencing. Our approach utilizes intron-targeted amplicon sequencing to characterise multi-locus intron polymorphisms (MIPs) and assess genetic diversity. These highly variable intron regions, combined with inter-specific transferable loci, serve as powerful multiple-SNP markers potentially suitable for various applications, from species and hybrid identification to population comparisons, without prior species knowledge. We developed the first panel of MIPs highly transferable across fish genomes, effectively distinguishing between species, even those closely related, and populations with different structures. MIPs offer versatile, hypervariable nuclear markers and promise to be especially useful when multiple nuclear loci must be genotyped across different species, such as for the monitoring of interspecific hybridization. Moreover, the relatively long sequences obtained ease the development of single-locus PCR-based diagnostic markers. This method, here demonstrated in teleost fishes, can be readily applied to other taxa, unlocking a new source of genetic variation.
对已知或疑似存在种间杂交或基因渗入现象的物种群体进行研究,需要分析双亲共同遗传的分子标记。目前的方法基于不同类别的标记,其中包括经典的微卫星标记,以及通过高通量测序分析数千个单核苷酸多态性(SNP)或数百个微单倍型的最新全基因组方法。我们的方法利用靶向内含子的扩增子测序来表征多位点内含子多态性(MIP)并评估遗传多样性。这些高度可变的内含子区域,结合种间可转移位点,可作为强大的多SNP标记,潜在适用于各种应用,从物种和杂交鉴定到群体比较,无需事先了解物种情况。我们开发了首个在鱼类基因组中高度可转移的MIP面板,能有效区分物种,即使是亲缘关系密切的物种,以及具有不同结构的群体。MIP提供了通用的、高度可变的核标记,并且当必须对不同物种的多个核基因座进行基因分型时,例如用于监测种间杂交,有望特别有用。此外,获得的相对较长的序列便于基于单基因座PCR的诊断标记的开发。这种方法在硬骨鱼中得到了验证,可轻松应用于其他分类群,从而开启了一个新的遗传变异来源。