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(R) evolution in the molecular sexing of ratite birds: identification and analysis of new candidate sex-linked markers

机译:(R)平胸鸟分子性别鉴定中的进化:新的候选性别相关标记的鉴定和分析

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The molecular methods for sex identification in birds are important resources commonly used in population studies, management and conservation plans, breeding programs and commercial poultry/farms. Recently, advanced polymerase chain reaction (PCR) methods based on melting curve analysis have been reported for Neognathae (non-ratite) birds. These genotyping strategies are simple, rapid, highly sensitive/specific and cost-effective, allowing high-throughput applicability. The evolutionary divergence and ancestral state of the sex chromosomes in the Palaeognathae (ratite) birds have hindered the utilisation of the sex-linked markers developed for non-ratite species. Therefore, the current PCR-based protocols for ratite species are restricted to agarose and polyacrylamide gels. The screening of new candidate sex-linked markers is mandatory to implement advanced PCR-based approaches in the routine molecular sexing of ratites. In this study, the nucleotide sequences of the Ostrich Z and W gametologous genes were used for the identification of new potential sex-linked markers, considering the optimisation of a molecular sexing protocol using the high-resolution melting (HRM) analysis. Four candidate markers (NTRK2, RASEF, TMEM2 and DAPK1) were characterised for four ratite species (Ostrich, Greater Rhea, Emu and Southern Cassowary). The male and female genotypes identified were accurately differentiated based on specific melting curve profiles generated. The discussion of the polymorphic patterns obtained and their influence on the reliability of molecular sexing are complemented with an overview of the classical PCR-based methods for ratite birds. This study highlights the potential and usefulness of the recently available genomic data for ratite sex chromosomes to identify new candidate sex-linked markers with simple in silico approaches.
机译:鸟类性别鉴定的分子方法是人口研究,管理和保护计划,育种计划和商业家禽/农场中常用的重要资源。近来,已经报道了基于新的熔解曲线分析的先进聚合酶链反应(PCR)方法用于Neognathae(非鼠兔)鸟类。这些基因分型策略简单,快速,高度敏感/特异且具有成本效益,可实现高通量应用。古猿类(无脊椎动物)鸟类中性染色体的进化差异和祖先状态阻碍了为非无脊椎动物物种开发的性相关标记的利用。因此,当前基于PCR的平胸动物实验方案仅限于琼脂糖和聚丙烯酰胺凝胶。必须对新的候选性别相关标记进行筛选,以在常规的常规分子性别鉴定中实施基于PCR的先进方法。在这项研究中,考虑到使用高分辨率熔解(HRM)分析优化分子性别鉴定方案,将鸵鸟Z和W配子同源基因的核苷酸序列用于鉴定新的潜在性别鉴定标记。四个候选标记(Ostrich,Great Rhea,Emu和Southern Cassowary)具有四个候选标记(NTRK2,RASEF,TMEM2和DAPK1)。根据生成的特定熔解曲线,可以准确地区分所鉴定的男性和女性基因型。对获得的多态性模式的讨论及其对分子性别区分可靠性的影响的补充是对基于等位基因鸟的经典基于PCR的方法的概述的补充。这项研究强调了最近可用的基因组数据对于平胸性染色体的潜力和实用性,可通过简单的计算机方法识别新的候选性连锁标记。

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