Zhang W J, Degli-Esposti M A, Cobain T J, Cameron P U, Christiansen F T, Dawkins R L
Department of Clinical Immunology, Royal Perth Hospital, Perth, Western Australia.
J Exp Med. 1990 Jun 1;171(6):2101-14. doi: 10.1084/jem.171.6.2101.
We have examined the hypothesis that MHC ancestral haplotypes have a specific content of genes regulating the extent of autoimmune reactions. Gene copy number was quantitated by objective densitometry after PFGE was used to separate heterozygous AHs of different lengths. Initially we analyzed examples of known gene copy number at the C4 and 21 hydroxylase loci and showed that the approach provides predictable results. We then studied heterozygotes containing one characterized and one uncharacterized AH with particular attention to the gene copy number at the C4, Cyp21, and DRB loci. Each AH studied has a characteristic gene copy number at each locus studied. The same may be true of TNF, but other possibilities must be considered. AHs are markers for extensive chromosomal segments including particular numbers of several functional genes. Since AHs mark susceptibility to autoimmune disease, differences in gene copy number may be implicated.
我们检验了这样一种假说,即主要组织相容性复合体(MHC)的祖先单倍型具有特定的基因含量,这些基因调控自身免疫反应的程度。在用脉冲场凝胶电泳(PFGE)分离不同长度的杂合祖先单倍型(AHs)后,通过客观密度测定法定量基因拷贝数。最初,我们分析了C4和21羟化酶基因座已知基因拷贝数的实例,并表明该方法可提供可预测的结果。然后,我们研究了含有一个已表征和一个未表征AH的杂合子,特别关注C4、Cyp21和DRB基因座的基因拷贝数。所研究的每个AH在每个研究基因座都有一个特征性的基因拷贝数。肿瘤坏死因子(TNF)可能也是如此,但必须考虑其他可能性。AHs是包括特定数量的几个功能基因在内的广泛染色体片段的标记。由于AHs标记了对自身免疫疾病的易感性,基因拷贝数的差异可能与之有关。