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人类主要组织相容性复合体的血清补体“超级基因”(补体型)

Serum complement 'supergenes' of the major histocompatibility complex in man (complotypes).

作者信息

Alper C A, Raum D, Karp S, Awdeh Z L, Yunis E J

出版信息

Vox Sang. 1983;45(1):62-7. doi: 10.1111/j.1423-0410.1983.tb04124.x.

Abstract

The loci for the complement proteins C2 and BF, and the two loci for C4 are closely linked to one another. In many hundreds of meioses no crossing over has been detected between these loci. In addition, the alleles of these four loci occur in specific combinations not predicted by their gene frequencies in much the same way as alleles of the Rh and MNS systems. These units are termed complotypes. There are 14 complotypes with frequencies in excess of 1% in our study population of normal sixth chromosomes from Caucasians. Since they are also intimately associated with HLA-DR, comploytypes may also be of importance in screening programs for transplantation.

摘要

补体蛋白C2和BF的基因座,以及C4的两个基因座彼此紧密连锁。在数百次减数分裂中,未检测到这些基因座之间发生交换。此外,这四个基因座的等位基因以特定组合出现,其方式并非由它们的基因频率所预测,这与Rh和MNS系统的等位基因情况非常相似。这些单位被称为补体型。在我们对白种人正常第六号染色体的研究群体中,有14种补体型的频率超过1%。由于它们也与HLA-DR密切相关,补体型在移植筛查项目中可能也很重要。

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