Partanen J
Finnish Red Cross Blood Transfusion Service, Tissue Typing Laboratory, Helsinki, Finland.
J Immunogenet. 1987 Dec;14(6):285-93. doi: 10.1111/j.1744-313x.1987.tb00393.x.
DNA polymorphism of the human major histocompatibility complex (MHC)-linked complement C4 genes was studied using restriction enzymes XbaI and TaqI, and Southern hybridization. The results show that some, but not all, C4 phenotypes can be divided into subtypes. Analysis of MHC haplotypes indicates that in each extended MHC haplotype, i.e. in the haplotypes having a particular combination of HLA and complotype phenotypes in significant linkage disequilibrium, the C4 genes always produce just one 'conserved' restriction enzyme fragment pattern, while in the other haplotypes the C4 genes are more heterogeneous. Furthermore, the findings provide preliminary evidence for a C4B gene duplication, and suggest that the C4 genes may often be 'corrected' alike.
使用限制性内切酶XbaI和TaqI以及Southern杂交技术,对人类主要组织相容性复合体(MHC)连锁的补体C4基因的DNA多态性进行了研究。结果表明,部分而非全部C4表型可分为亚型。对MHC单倍型的分析表明,在每个扩展的MHC单倍型中,即在具有显著连锁不平衡的特定HLA和补体型表型组合的单倍型中,C4基因总是产生一种“保守的”限制性酶切片段模式,而在其他单倍型中,C4基因则更为异质。此外,这些发现为C4B基因重复提供了初步证据,并表明C4基因可能经常以相似的方式“校正”。