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MHC III类基因的多态性:限制性片段连锁群的定义以及频繁缺失和重复的证据。

Polymorphism of MHC class III genes: definition of restriction fragment linkage groups and evidence for frequent deletions and duplications.

作者信息

Ghanem N, Uring-Lambert B, Abbal M, Hauptmann G, Lefranc M P, Lefranc G

机构信息

Laboratoire d'Immunogénétique, UA CNRS 1191 Génétique Moléculaire, Université des Sciences et Techniques du Languedoc, Montpellier, France.

出版信息

Hum Genet. 1988 Jul;79(3):209-18. doi: 10.1007/BF00366239.

Abstract

The loci for the complement proteins BF and C2 and the two loci for C4 are closely linked to one another, as are the duplicated steroid 21 hydroxylase (21-OHase) genes to the C4A and C4B loci. The alleles of these four loci occur in specific combinations termed "complotypes". We have studied the gene frequencies of their different products in the Lebanese population and compared these values with those found in other populations. We observed a novel complotype (S B 4 6) in one family and a complotype with a so far undescribed variant of the C4A locus. Using several restriction fragment length polymorphisms (RFLPs), we have defined restriction fragment linkage groups. The combined use of C4 and 21-OHase probes allowed us to detect different types of deletions and duplications at these loci in the Lebanese population.

摘要

补体蛋白BF和C2的基因座以及C4的两个基因座彼此紧密连锁,重复的类固醇21羟化酶(21-OHase)基因与C4A和C4B基因座也是如此。这四个基因座的等位基因以特定组合出现,称为“复合单体型”。我们研究了黎巴嫩人群中它们不同产物的基因频率,并将这些值与其他人群中的值进行了比较。我们在一个家族中观察到一种新的复合单体型(S B 4 6)和一种具有迄今未描述的C4A基因座变体的复合单体型。使用几种限制性片段长度多态性(RFLP),我们定义了限制性片段连锁群。C4和21-OHase探针的联合使用使我们能够在黎巴嫩人群中检测到这些基因座处不同类型的缺失和重复。

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