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沙特人群中γ-珠蛋白基因区域的Xmn I多态性

Xmn I polymorphism in the gamma-globin gene region among Saudis.

作者信息

el-Hazmi M A

机构信息

Medical Biochemistry Department, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, Saudi Arabia.

出版信息

Hum Hered. 1989;39(1):12-9. doi: 10.1159/000153825.

Abstract

The gamma-globin chains of haemoglobin F are encoded by two non-allelic genes which synthesise two different gamma-chains referred to as G gamma and A gamma. Xmn I restricts on both sides of the genes and normally produces an 8.1-kilobase (kb) fragment containing both gamma-genes. A polymorphic site on the 5' end of the G gamma genes has been reported in some populations and it results in the production of a 7.0-kb fragment containing both gamma-genes. We investigated the Xmn I polymorphic site in normal individuals, haemoglobin S heterozygotes and sickle cell disease patients from three different regions of Saudi Arabia. In the eastern province, 10% of gamma-genes in normal individuals were linked to the 7.0-kb fragment while in the sickle cell disease patients and haemoglobin S heterozygotes the frequency of the polymorphic site was 0.932 and 0.625, respectively. In the south-western province, the frequency of the polymorphic site in normal individuals was 0.096 (similar to that in the eastern province) but in the sickle cell disease patients and sickle cell heterozygotes the frequency was 0.033 and 0.095, respectively. Finally, only 6 sickle cell disease patients from the north-western province were investigated and all had the gamma-globin gene linked to the 8.1-kb fragment. The results of this study in different regions of Saudi Arabia are presented and the possible significance of Xmn I polymorphism is suggested.

摘要

血红蛋白F的γ-珠蛋白链由两个非等位基因编码,这两个基因合成两种不同的γ-链,分别称为Gγ和Aγ。Xmn I在这两个基因的两侧进行切割,通常会产生一个包含两个γ-基因的8.1千碱基(kb)片段。在一些人群中,已报道Gγ基因5'端存在一个多态性位点,该位点会产生一个包含两个γ-基因的7.0 kb片段。我们对来自沙特阿拉伯三个不同地区的正常个体、血红蛋白S杂合子和镰状细胞病患者的Xmn I多态性位点进行了研究。在东部省份,正常个体中10%的γ-基因与7.0 kb片段相连,而在镰状细胞病患者和血红蛋白S杂合子中,多态性位点的频率分别为0.932和0.625。在西南部省份,正常个体中多态性位点的频率为0.096(与东部省份相似),但在镰状细胞病患者和镰状细胞杂合子中,频率分别为0.033和0.095。最后,仅对来自西北部省份的6例镰状细胞病患者进行了研究,所有患者的γ-珠蛋白基因均与8.1 kb片段相连。本文展示了沙特阿拉伯不同地区的这项研究结果,并提出了Xmn I多态性的可能意义。

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