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荷兰β地中海贫血:一种与大量γ链产生相关的10千碱基DNA缺失。

Dutch beta 0-thalassaemia: a 10 kilobase DNA deletion associated with significant gamma-chain production.

作者信息

Gilman J G, Huisman T H, Abels J

出版信息

Br J Haematol. 1984 Feb;56(2):339-48. doi: 10.1111/j.1365-2141.1984.tb03961.x.

Abstract

A unique beta 0-thalassaemia in a Dutch family results in fetal haemoglobin expression comparable to that of delta 0 beta 0-thalassaemia. Haemoglobin analysis and restriction endonuclease mapping studies of DNA suggest that the beta-globin gene is entirely deleted, but that the delta-globin gene is intact. The 5' break point of the deletion is 3-4 kilobases 3' to the delta-globin gene, while the 3' break point is 6-7 kilobases 3' to the beta-globin gene (relative to the normal DNA restriction map). The result is a approximately 10 kilobase deletion of DNA whose 3' end point may lie very close to that for one delta 0 beta 0-thalassaemia, within a cluster of Kpn I-family repetitive sequences. The Dutch beta 0-thalassaemia deletion is thus the shortest one which, in the absence of additional chromosomal rearrangements, results in enhancement of gamma-chain synthesis above that seen for haemoglobin Lepore. These data support the hypothesis that the region of DNA 3' to the beta-globin gene may be important to the developmental regulation of fetal gamma versus adult beta chain production.

摘要

荷兰一个家族中出现的一种独特的β⁰地中海贫血,其胎儿血红蛋白表达水平与δ⁰β⁰地中海贫血相当。血红蛋白分析和DNA限制性内切酶图谱研究表明,β珠蛋白基因完全缺失,但δ珠蛋白基因完整。缺失的5'断点位于δ珠蛋白基因下游3 - 4千碱基处,而3'断点位于β珠蛋白基因下游6 - 7千碱基处(相对于正常DNA限制性图谱)。结果是约10千碱基的DNA缺失,其3'端点可能与一种δ⁰β⁰地中海贫血的端点非常接近,位于Kpn I家族重复序列簇内。因此,荷兰β⁰地中海贫血缺失是最短的一种,在没有额外染色体重排的情况下,会导致γ链合成增强,超过血红蛋白Lepore的水平。这些数据支持了这样的假说,即β珠蛋白基因下游的DNA区域可能对胎儿γ链与成人β链产生的发育调控很重要。

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