Institute of Environmental Sciences, Jagiellonian University, Gronostajowa 7, 30-387 Kraków, Poland.
Mol Ecol Resour. 2010 Mar;10(2):237-51. doi: 10.1111/j.1755-0998.2009.02788.x. Epub 2009 Oct 15.
Genes of the major histocompatibility complex (MHC) are considered a paradigm of adaptive evolution at the molecular level and as such are frequently investigated by evolutionary biologists and ecologists. Accurate genotyping is essential for understanding of the role that MHC variation plays in natural populations, but may be extremely challenging. Here, I discuss the DNA-based methods currently used for genotyping MHC in non-model vertebrates, as well as techniques likely to find widespread use in the future. I also highlight the aspects of MHC structure that are relevant for genotyping, and detail the challenges posed by the complex genomic organization and high sequence variation of MHC loci. Special emphasis is placed on designing appropriate PCR primers, accounting for artefacts and the problem of genotyping alleles from multiple, co-amplifying loci, a strategy which is frequently necessary due to the structure of the MHC. The suitability of typing techniques is compared in various research situations, strategies for efficient genotyping are discussed and areas of likely progress in future are identified. This review addresses the well established typing methods such as the Single Strand Conformation Polymorphism (SSCP), Denaturing Gradient Gel Electrophoresis (DGGE), Reference Strand Conformational Analysis (RSCA) and cloning of PCR products. In addition, it includes the intriguing possibility of direct amplicon sequencing followed by the computational inference of alleles and also next generation sequencing (NGS) technologies; the latter technique may, in the future, find widespread use in typing complex multilocus MHC systems.
主要组织相容性复合体(MHC)的基因被认为是分子水平上适应性进化的典范,因此经常受到进化生物学家和生态学家的研究。准确的基因分型对于理解 MHC 变异在自然种群中的作用至关重要,但可能极具挑战性。在这里,我讨论了目前用于非模式脊椎动物 MHC 基因分型的基于 DNA 的方法,以及未来可能广泛使用的技术。我还强调了与基因分型相关的 MHC 结构方面,并详细介绍了 MHC 基因座复杂的基因组组织和高度的序列变异所带来的挑战。特别强调了设计适当的 PCR 引物,考虑到可能出现的人工制品以及从多个共同扩增的基因座中基因分型等位基因的问题,由于 MHC 的结构,这种策略经常是必要的。在各种研究情况下比较了分型技术的适用性,讨论了高效基因分型的策略,并确定了未来可能取得进展的领域。本综述涉及单链构象多态性(SSCP)、变性梯度凝胶电泳(DGGE)、参考链构象分析(RSCA)和 PCR 产物克隆等已建立的分型方法。此外,它还包括直接扩增子测序后通过计算推断等位基因的有趣可能性,以及下一代测序(NGS)技术;该技术将来可能会在复杂的多基因座 MHC 系统的分型中得到广泛应用。