Saha B K
Department of Pathology, Emory University School of Medicine, Atlanta, GA 30322, USA.
J Immunol Methods. 1996 Jul 17;194(1):77-83. doi: 10.1016/0022-1759(96)00065-8.
Two DNA-based assays were developed for identification of the H2 alleles present in the 12 standard mouse MHC haplotypes H2b, H2d, H2f, H2j, H2k, H2p, H2q, H2r, H2s, H2u, H2v and H2z. The assays utilized polymerase chain reaction (PCR) amplification of a short stretch of genomic DNA including a highly polymorphic microsatellite from the second intron of the class II Eb gene within the murine major histocompatibility complex. The H2 Eb alleles were discerned by restriction fragment length polymorphism (RFLP) and heteroduplex analyses. For RFLP analysis amplified DNAs were digested with the restriction endonuclease Fnu4HI which delineated seven of the 12 alleles. A distinct pattern was obtained for the haplotypes H2d, H2j, H2k and H2p, whereas a group specific but distinct pattern was obtained for each of the three groups H2b, H2r and H2v, H2f, H2q and H2s, H2u and H2z. Heteroduplex analysis using a pair of haplotypes at a time helped further discriminate H2q from H2f or H2s. More importantly, heteroduplexing was quite informative in delineating the identity or disparity between two given haplotypes in a single step of PCR amplification. Both the RFLP and heteroduplex analyses are extremely sensitive and simple to operate, and since the target is genomic DNA, they can be carried out using any cell or tissue type.
开发了两种基于DNA的检测方法,用于鉴定存在于12种标准小鼠MHC单倍型H2b、H2d、H2f、H2j、H2k、H2p、H2q、H2r、H2s、H2u、H2v和H2z中的H2等位基因。这些检测方法利用聚合酶链反应(PCR)扩增一小段基因组DNA,该DNA包含来自小鼠主要组织相容性复合体中II类Eb基因第二个内含子的高度多态性微卫星。通过限制性片段长度多态性(RFLP)和异源双链分析来识别H2 Eb等位基因。对于RFLP分析,扩增的DNA用限制性内切酶Fnu4HI消化,该酶可区分12个等位基因中的7个。对于单倍型H2d、H2j、H2k和H2p获得了独特的模式,而对于H2b、H2r和H2v、H2f、H2q和H2s、H2u和H2z这三组中的每一组都获得了组特异性但独特的模式。一次使用一对单倍型的异源双链分析有助于进一步区分H2q与H2f或H2s。更重要的是,异源双链分析在单个PCR扩增步骤中描绘两个给定单倍型之间的相同或差异方面非常有用。RFLP和异源双链分析都极其灵敏且操作简单,并且由于靶标是基因组DNA,因此可以使用任何细胞或组织类型进行检测。