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一个患有溶血性贫血且有三种β珠蛋白的家族:血红蛋白亚特兰大-考文垂缺失(β75亮氨酸→脯氨酸,141位亮氨酸缺失)在核苷酸水平不存在。

A family with haemolytic anaemia and three beta-globins: the deletion in haemoglobin Atlanta-Coventry (beta 75 Leu----Pro, 141 Leu deleted) is not present at the nucleotide level.

作者信息

George P M, Myles T, Williamson D, Higuchi R, Symmans W A, Brennan S O

机构信息

Molecular Pathology Laboratory, Christchurch Hospital, New Zealand.

出版信息

Br J Haematol. 1992 May;81(1):93-8. doi: 10.1111/j.1365-2141.1992.tb08178.x.

Abstract

Analyses of haemoglobin from a family with an unstable haemoglobin haemolytic anaemia demonstrated that the affected individuals had three beta-globins, namely, normal (beta A), Atlanta (beta At) with a mutation of beta 75 Leu----Pro, and beta-Atlanta-Coventry (beta At-Co) with mutation of beta 75 Leu----Pro and beta 141 Leu deleted. These were present in the ratio 66:23:11 respectively. The structure of the beta-globin cluster, however, was found to be normal by Southern blotting; also cytogenetic analysis failed to show any abnormality. DNA sequence analyses demonstrated the presence of the beta At mutation in genomic DNA isolated from leucocytes but the Coventry deletion of 141 Leu in beta At-Co was not present in genomic DNA. PCR amplification of the beta-globin cDNA and direct sequencing of the product also failed to demonstrate the Coventry deletion. Thus, it appears that the absence of 141 Leu in the beta At-Co globin is a consequence of the beta At mutation in these patients and that both beta At and beta At-Co are the product of a single gene. This unusual conclusion is paralleled in the bizarre case of Hb Vicksburg where the deletion of a leucine at beta 75 is not coded for in genomic DNA.

摘要

对一个患有不稳定血红蛋白溶血性贫血家族的血红蛋白分析表明,受影响个体有三种β-珠蛋白,即正常的(βA)、在β75位有亮氨酸突变为脯氨酸的亚特兰大(βAt)以及β75位亮氨酸突变为脯氨酸且β141位亮氨酸缺失的β-亚特兰大-考文垂(βAt-Co)。它们分别以66:23:11的比例存在。然而,通过Southern印迹法发现β-珠蛋白基因簇的结构正常;细胞遗传学分析也未显示任何异常。DNA序列分析表明,从白细胞中分离的基因组DNA中存在βAt突变,但βAt-Co中β141位亮氨酸的考文垂缺失在基因组DNA中不存在。β-珠蛋白cDNA的PCR扩增及产物的直接测序也未能证实考文垂缺失。因此,似乎在这些患者中βAt-Co珠蛋白中β141位亮氨酸的缺失是βAt突变的结果,并且βAt和βAt-Co都是单个基因的产物。这一不同寻常的结论在Hb维克斯堡的奇特病例中也有类似情况,即β75位亮氨酸的缺失在基因组DNA中没有编码。

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