Pichon L, Carn G, Bouric P, Giffon T, Chauvel B, Lepourcelet M, Mosser J, Legall J Y, David V
Department of Biochemistry and Molecular Biology, CNRS, Recombinaisons genetiques, Rennes, France.
Genomics. 1996 Mar 1;32(2):236-44. doi: 10.1006/geno.1996.0110.
Positional cloning strategies for the hemochromatosis gene have previously concentrated on a target area restricted to a maximum genomic expanse of 400 kb around the HLA-A and HLA-F loci. Recently, the candidate region has been extended to 2-3 Mb on the distal side of the MHC. In this study, 10 coding sequences [hemochromatosis candidate genes (HCG) I to X] were isolated by cDNA selection using YACs covering the HLA-A/HLA-F subregion. Two of these (HCG II and HCG IV) belong to multigene families, as well as other sequences already described in this region, i.e., P5, pMC 6.7, and HLA class 1. Fingerprinting of the four YACs overlapping the region was performed and allowed partial localization of the different multigene family sequences on each YAC without defining their exact positions. Fingerprinting on cosmids isolated from the ICRF chromosome 6-specific cosmid library allowed more precise localization of the redundant sequences in all of the multigene families and revealed their apparent organization in clusters. Further examination of these intertwined sequences demonstrated that this structural organization resulted from a succession of complex phenomena, including duplications and contractions. This study presents a precise description of the structural organization of the HLA-A/HLA-F region and a determination of the sequences involved in the megabase size polymorphism observed among the A3, A24, and A31 haplotypes.
此前,血色素沉着病基因的定位克隆策略主要集中在一个目标区域,该区域限制在HLA - A和HLA - F基因座周围最大400 kb的基因组范围内。最近,候选区域已扩展到MHC远端的2 - 3 Mb。在本研究中,通过使用覆盖HLA - A/HLA - F亚区域的酵母人工染色体(YAC)进行cDNA筛选,分离出了10个编码序列[血色素沉着病候选基因(HCG)I至X]。其中两个(HCG II和HCG IV)属于多基因家族,该区域中已描述的其他序列也是如此,即P5、pMC 6.7和HLA I类。对与该区域重叠的四个YAC进行了指纹分析,使得不同多基因家族序列在每个YAC上得到了部分定位,但未确定它们的确切位置。对从ICRF 6号染色体特异性黏粒文库中分离出的黏粒进行指纹分析,能够更精确地定位所有多基因家族中的冗余序列,并揭示它们明显的成簇组织方式。对这些相互交织的序列进行进一步研究表明,这种结构组织是由一系列复杂现象导致的,包括重复和收缩。本研究对HLA - A/HLA - F区域的结构组织进行了精确描述,并确定了在A3、A24和A31单倍型中观察到的兆碱基大小多态性所涉及的序列。