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从凝血因子VIII基因(F8C)到红/绿色觉,跨越Xq28的葡萄糖-6-磷酸脱氢酶(G6PD)单倍型。

G6PD haplotypes spanning Xq28 from F8C to red/green color vision.

作者信息

Filosa S, Calabrò V, Lania G, Vulliamy T J, Brancati C, Tagarelli A, Luzzatto L, Martini G

机构信息

Istituto Internazionale di Genetica e Biofisica, CNR, Naples, Italy.

出版信息

Genomics. 1993 Jul;17(1):6-14. doi: 10.1006/geno.1993.1276.

Abstract

The most telomeric region of the human X chromosome within band Xq28 consists of a gene-rich region of about 3 Mb which contains the genes for coagulation factor VIIIc, glucose-6-phosphate dehydrogenase (G6PD), and red/green color vision. We have studied five polymorphic sites from this region, in a sample of normal people from the Cosenza province of Southern Italy. These sites, which span a distance of some 350 kb, are in strong linkage disequilibrium. Of the 32 possible haplotypes only 10 were found, and 4 of these account for 80% of all X chromosomes analyzed. In addition, we found that all G6PD-deficient people with the G6PD Mediterranean mutation belong to only two haplotypes. One of these (Med 1) is found only within a small subregion of the area investigated, west of the Appennine mountain range. Most remarkably, all Med 1 G6PD-deficient individuals also had red/green color blindness. The more frequent haplotype (Med 2) is the same in Calabria and in Sardinia, where it accounts for about 90% of the G6PD Mediterranean mutations, despite the fact that gene flow between the populations of Sardinia and Southern Italy must have been limited. These data do not enable us to determine whether the two types of G6PD Mediterranean have arisen through two separate identical mutational events or through a single mutational event followed by recombination. However, the data indicate relatively little recombination over an extended region of the X chromosome and they suggest that the G6PD Mediterranean mutation is recent by comparison to the other polymorphisms investigated.

摘要

人类X染色体Xq28带内最末端的区域由一个约3 Mb的基因丰富区域组成,该区域包含凝血因子VIIIc、葡萄糖-6-磷酸脱氢酶(G6PD)以及红/绿色觉相关的基因。我们在来自意大利南部科森扎省的正常人群样本中,研究了该区域的五个多态性位点。这些位点跨度约350 kb,处于强连锁不平衡状态。在32种可能的单倍型中,仅发现了10种,其中4种占所有分析的X染色体的80%。此外,我们发现所有携带G6PD地中海突变的G6PD缺乏症患者仅属于两种单倍型。其中一种(Med 1)仅在亚平宁山脉以西所研究区域的一个小亚区域内发现。最值得注意的是,所有携带Med 1的G6PD缺乏症个体也患有红/绿色盲。更常见的单倍型(Med 2)在卡拉布里亚和撒丁岛相同,在那里它占G6PD地中海突变的约90%,尽管撒丁岛和意大利南部人群之间的基因流动必定有限。这些数据无法让我们确定两种类型的G6PD地中海突变是通过两个独立的相同突变事件产生的,还是通过一个突变事件后再发生重组产生的。然而,数据表明在X染色体的一个扩展区域内重组相对较少,并且它们表明与所研究的其他多态性相比,G6PD地中海突变是近期发生的。

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