Guillaudeux T, Janer M, Wong G K, Spies T, Geraghty D E
The Clinical Research Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue, D2-100, Seattle WA 98109, USA.
Proc Natl Acad Sci U S A. 1998 Aug 4;95(16):9494-9. doi: 10.1073/pnas.95.16.9494.
We report here the genomic sequence of the centromeric portion of HLA class I, extending 424,015 bp from tumor necrosis factor alpha to a newly identified gene approximately 20 kb telomeric of Otf-3. As a source of DNA, we used cosmids centromeric of HLA-B that had been mapped previously with conventional restriction digestion and fingerprinting and previously characterized yeast artificial chromosomes subcloned into cosmids and mapped with multiple complete digest methodologies. The data presented provide a description of the gene content of centromeric HLA class I including new data on intron, promoter and flanking sequences of previously described genes, and a description of putative new genes that remain to be characterized beyond the structural information uncovered. A complete accounting of the repeat structure including abundant di-, tri-, and tetranucleotide microsatellite loci yielded access to precisely localized mapping tools for the major histocompatibility complex. Comparative analysis of a highly polymorphic region between HLA-B and -C was carried out by sequencing over 40 kb of overlapping sequence from two haplotypes. The levels of variation observed were much higher than those seen in other regions of the genome and indeed were higher than those observed between allelic HLA class I loci.
我们在此报告 HLA Ⅰ类基因着丝粒部分的基因组序列,该序列从肿瘤坏死因子α延伸 424,015 碱基对至 Otf - 3 端粒方向约 20 kb 处新发现的一个基因。作为 DNA 来源,我们使用了先前通过传统限制性酶切和指纹图谱定位的 HLA - B 着丝粒粘粒,以及先前已鉴定的酵母人工染色体,这些酵母人工染色体已亚克隆到粘粒中,并通过多种完全酶切方法进行了定位。所呈现的数据描述了着丝粒 HLA Ⅰ类基因的基因内容,包括先前描述基因的内含子、启动子和侧翼序列的新数据,以及对有待在已揭示的结构信息之外进行特征鉴定的假定新基因的描述。对包括丰富的二核苷酸、三核苷酸和四核苷酸微卫星位点在内的重复结构进行全面分析,获得了用于主要组织相容性复合体精确定位的图谱工具。通过对来自两个单倍型的 40 kb 以上重叠序列进行测序,对 HLA - B 和 - C 之间的一个高度多态区域进行了比较分析。观察到的变异水平远高于基因组其他区域,实际上也高于 HLA Ⅰ类等位基因位点之间观察到的变异水平。