Department of Medicine, Division of Nephrology, University of Virginia School of Medicine, Charlottesville, VA 22908, USA.
Immunogenetics. 2012 Aug;64(8):633-40. doi: 10.1007/s00251-012-0630-4. Epub 2012 Jul 1.
Ly49G and H-2 class I D(k) molecules are critical to natural killer cell-mediated viral control. To examine their contributions in greater depth, we established NK gene complex (NKC)/Ly49 congenic strains and a novel genetic model defined by MHC class I D(k) disparity in congenic and transgenic mouse strains. Generation and maintenance of Ly49 and H-2 class I select strains require efficient and reproducible genotyping assays for highly polygenic and polymorphic sequences. Thus, we coupled gene- and allele-specific PCR with high-resolution melt (HRM) analysis to discriminate Ly49g and H-2 class I D and K alleles in select strains and in the F(2) and backcross hybrid offspring of different genetic crosses. We show that HRM typing for these critical immune response genes is fast, accurate, and dependable. We further demonstrate that H-2 class I D HRM typing is competent to detect and quantify transgene copy numbers in different mice with distinct genetic backgrounds. Our findings substantiate the utility and practicality of HRM genotyping for highly related genes and alleles, even those belonging to clustered multigene families. Based on these findings, we envision that HRM is capable to interrogate and quantify gene- and allele-specific variations due to differential regulation of gene expression.
Ly49G 和 H-2 类 I D(k) 分子对于自然杀伤细胞介导的病毒控制至关重要。为了更深入地研究它们的作用,我们建立了 NK 基因复合物(NKC)/Ly49 同基因系,并建立了一种新的遗传模型,该模型定义为 MHC 类 I D(k) 在同基因和转基因小鼠系中的差异。Ly49 和 H-2 类 I 选择株的产生和维持需要高效且可重复的基因分型测定,以区分高度多态性和多态性序列的基因和等位基因。因此,我们将基因和等位基因特异性 PCR 与高分辨率熔解(HRM)分析相结合,以区分选择株以及不同遗传杂交的 F(2) 和回交杂种后代中的 Ly49g 和 H-2 类 I D 和 K 等位基因。我们证明了这些关键免疫反应基因的 HRM 分型快速、准确且可靠。我们进一步证明,H-2 类 I D HRM 分型能够检测和定量不同遗传背景的不同小鼠中的转基因拷贝数。我们的研究结果证实了 HRM 基因分型对于高度相关的基因和等位基因(甚至属于聚类多基因家族的基因和等位基因)的实用性和实用性。基于这些发现,我们设想 HRM 能够检测和定量由于基因表达差异调控而导致的基因和等位基因特异性变异。