Kambhu S, Falldorf P, Lee J S
Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10021.
Proc Natl Acad Sci U S A. 1990 Jul;87(13):4927-31. doi: 10.1073/pnas.87.13.4927.
Two endogenous retroviral long terminal repeats (LTRs) were found in the human major histocompatibility complex locus HLA-DQ. The solo LTRs, unlinked to retrovirus structural genes, are located approximately 5 kilobases apart from each other and in the same transcriptional orientation, which is opposite to that for the HLA-DQB1 gene. These elements exhibit greater than 90% homology to the LTRs of the human endogenous retrovirus HERV-K10. The conservation of putative regulatory elements found within the LTRs and their position relative to the HLA-DQB1 gene suggest that these elements may confer distinct regulatory properties on genes in the HLA-DQ region. Polymorphic variation between different HLA haplotypes for the presence of the LTRs at this location and of the molecular architecture within this subregion is supported by polymerase chain reaction and Southern blot analysis. Comparisons of chromosomes with and without the LTRs in this region will provide a unique opportunity in the human genome to analyze transposition or integration of retroviral sequences.
在人类主要组织相容性复合体基因座HLA - DQ中发现了两个内源性逆转录病毒长末端重复序列(LTRs)。这些单独的LTRs与逆转录病毒结构基因不连锁,彼此相距约5千碱基,且转录方向相同,这与HLA - DQB1基因的转录方向相反。这些元件与人类内源性逆转录病毒HERV - K10的LTRs具有超过90%的同源性。LTRs中发现的假定调控元件的保守性及其相对于HLA - DQB1基因的位置表明,这些元件可能赋予HLA - DQ区域基因独特的调控特性。聚合酶链反应和Southern印迹分析证实了不同HLA单倍型在该位置LTRs的存在以及该亚区域内分子结构的多态性变异。比较该区域有无LTRs的染色体将为人类基因组分析逆转录病毒序列的转座或整合提供独特机会。