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一个患有β地中海贫血的爱尔兰家庭中的减数分裂重组

Meiotic recombination in an Irish family with beta-thalassaemia.

作者信息

Hall G W, Sampietro M, Barnetson R, Fitzgerald J, McCann S, Thein S L

机构信息

MRC Molecular Haematology Unit, John Radcliffe Hospital, Headington, Oxford, UK.

出版信息

Hum Genet. 1993 Aug;92(1):28-32. doi: 10.1007/BF00216141.

Abstract

Using the technique of allele-specific priming of the polymerase chain reaction (PCR), the C-T substitution in codon 39 was identified as the cause of beta-thalassaemia in an Irish family. Analysis of the restriction fragment length polymorphisms (RFLPs) in the beta-globin gene cluster established linkage of the beta-thalassaemia mutation to a particular beta-haplotype but indicated that a recombinational event had occurred in the paternal chromosome in the younger of two affected children. Non-paternity was excluded by DNA fingerprinting analysis with hypervariable minisatellite probes. This is the fourth case of recombination in the beta-globin gene cluster to be reported. The event has occurred 5' of the polymorphic RsaI site at position -550 bp upstream of the beta-globin gene mRNA Cap site, within the 9.1-kb region that has been shown to be a hot spot for recombination in the beta-globin gene cluster.

摘要

运用聚合酶链反应(PCR)的等位基因特异性引物技术,在一个爱尔兰家庭中确定了密码子39处的C-T替换是β地中海贫血的病因。对β珠蛋白基因簇中限制性片段长度多态性(RFLP)的分析确定了β地中海贫血突变与特定β单倍型的连锁关系,但表明在两个患病儿童中年龄较小者的父本染色体上发生了一次重组事件。通过使用高变微卫星探针的DNA指纹分析排除了非父系情况。这是报道的β珠蛋白基因簇中第四例重组情况。该事件发生在β珠蛋白基因mRNA帽位点上游-550 bp处多态性RsaI位点的5'端,位于已被证明是β珠蛋白基因簇中重组热点的9.1 kb区域内。

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