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与主要组织相容性复合体(MHC)相关的Ⅲ类基因。德国高加索人群中C4基因频率、补体单倍型及其与不同HLA单倍型的关联分析。

MHC-linked class III genes. Analysis of C4 gene frequencies, complotypes and associations with distinct HLA haplotypes in German Caucasians.

作者信息

Schendel D J, O'Neill G J, Wank R

出版信息

Immunogenetics. 1984;20(1):23-31. doi: 10.1007/BF00373444.

Abstract

The class III complement components, C4, C2 and factor B (BF), are encoded in the human major histocompatibility complex (MHC). The two genes determining C4 (C4A and C4B) display considerable polymorphism and, thus, are important markers for HLA. In combination with alleles of C2 and BF they can be grouped into unique complotypes. We have analyzed the C4 alleles in a panel of 204 unrelated German Caucasians and studied their segregation with HLA haplotypes in 24 normal families. Inclusion of the class III markers with the class I and II alleles provides a more refined picture of the genetic structure of the MHC in these families. When charted according to the HLA-B locus specificities the MHCs can be clustered into groups showing distinctly homogenous or heterogenous complotypes. The identification of such groups is valuable for the selection of genetic material to analyze the molecular genetics of the human MHC.

摘要

Ⅲ类补体成分C4、C2和B因子(BF)在人类主要组织相容性复合体(MHC)中编码。决定C4的两个基因(C4A和C4B)表现出相当大的多态性,因此是HLA的重要标志物。与C2和BF的等位基因相结合,它们可以被归为独特的补体型。我们分析了204名无关德国白种人的C4等位基因,并在24个正常家庭中研究了它们与HLA单倍型的分离情况。将Ⅲ类标记与Ⅰ类和Ⅱ类等位基因一起纳入,能更清晰地呈现这些家庭中MHC的遗传结构。根据HLA - B位点特异性绘制图谱时,MHC可聚类成显示明显同质或异质补体型的组。识别这些组对于选择遗传物质以分析人类MHC的分子遗传学很有价值。

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