Kulski Jerzy K, Shigenari Atsuko, Shiina Takashi, Hosomichi Kazuyoshi, Yawata Makoto, Inoko Hidetoshi
Centre for Forensic Science, The University of Western Australia, Crawley, Western Australia, Australia.
Immunogenetics. 2009 Apr;61(4):257-70. doi: 10.1007/s00251-009-0364-0. Epub 2009 Mar 18.
The study of the association of the Human Leukocyte Antigen (HLA) alleles and polymorphic retrotransposons such as Alu, HERV, and LTR at various loci within the Major Histocompatibility Complex allows for a better identification and stratification of disease associations and the origins of HLA haplotypes in different populations. This paper provides sequence and association data on two structurally polymorphic MER9-LTR retrotransposons that are located 54 kb apart and in close proximity to the multiallelic HLA-A gene involved in the regulation of the human immune system. Direct DNA sequencing and analysis of the PCR products identified DNA nucleotide variations between the MER9-LTR sequences at the two loci and their associations with HLA-A alleles as potential haplotype and evolutionary markers. All MER9-LTR sequences were haplotypic when associated with common HLA-A alleles. The number of SNP loci was 2.5 times greater for the solo LTR at the AK locus, which is located closer to the HLA-A gene than the solo or 3' LTR at the HG locus. Our study shows that the nucleotide variations of the MER9-LTR DNA sequences are additional informative markers in fine mapping HLA-A genomic haplotypes for future population, evolutionary, and disease studies.
对主要组织相容性复合体中不同位点的人类白细胞抗原(HLA)等位基因与Alu、HERV和LTR等多态性逆转座子之间关联的研究,有助于更好地识别和分层疾病关联以及不同人群中HLA单倍型的起源。本文提供了关于两个结构多态性MER9-LTR逆转座子的序列和关联数据,它们相距54 kb,且紧邻参与人类免疫系统调节的多等位基因HLA-A基因。对PCR产物进行直接DNA测序和分析,确定了两个位点的MER9-LTR序列之间的DNA核苷酸变异及其与HLA-A等位基因的关联,作为潜在的单倍型和进化标记。当与常见的HLA-A等位基因相关联时,所有MER9-LTR序列都是单倍型的。位于比HG位点的单独LTR或3' LTR更靠近HLA-A基因的AK位点的单独LTR的SNP位点数量,是HG位点的2.5倍。我们的研究表明,MER9-LTR DNA序列的核苷酸变异是未来人群、进化和疾病研究中精细定位HLA-A基因组单倍型时的额外信息标记。