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人类β-珠蛋白基因5'侧翼区的DNA序列:进化保守性与多态性差异

The DNA sequence of the 5' flanking region of the human beta-globin gene: evolutionary conservation and polymorphic differences.

作者信息

Moschonas N, de Boer E, Flavell R A

出版信息

Nucleic Acids Res. 1982 Mar 25;10(6):2109-20. doi: 10.1093/nar/10.6.2109.

Abstract

We have determined the DNA sequence of a 1464 bp segment immediately flanking the 5' side of the human beta-globin gene. The sequence shows little similarity to the corresponding regions of the epsilon- or gamma-globin genes. There is about 75% homology, however, between the 5' extragenic regions of the beta-globin genes of man, goat and rabbit respectively. The mouse beta minor globin gene, but not the mouse beta major globin gene, also shares this extensive homology. A short segment of simple sequence DNA is found from about 1418 to 1388 bp upstream from the human beta-globin gene which consists of repeats of the sequence (TTTTA). Similar DNA sequences are also found at several sites in the large intron of the beta-globin gene. We have compared the DNA sequence of the 5' extragenic region of the normal beta-globin gene with the same segment of the beta-globin gene of a patient with beta thalassaemia. Of the two nucleotide differences observed, one generates a polymorphic HinfI site present 990 bp upstream from the beta-globin gene in the thalassaemic beta-globin and absent in the normal gene. A second beta thalassemic beta-globin gene which has the same molecular defect as the above mentioned case, however, lacks this HinfI site. It is therefore not yet clear whether this HinfI site will have any value in prenatal diagnosis of beta thalassaemia.

摘要

我们已经测定了人β-珠蛋白基因5'端紧邻的一段1464bp片段的DNA序列。该序列与ε-或γ-珠蛋白基因的相应区域几乎没有相似性。然而,人、山羊和兔子的β-珠蛋白基因的5'基因外区域之间分别有约75%的同源性。小鼠β-珠蛋白小基因而非β-珠蛋白大基因也具有这种广泛的同源性。在人β-珠蛋白基因上游约1418至1388bp处发现了一段短的简单序列DNA,其由序列(TTTTA)的重复组成。在β-珠蛋白基因的大内含子中的几个位点也发现了类似的DNA序列。我们已经将正常β-珠蛋白基因的5'基因外区域的DNA序列与一名β地中海贫血患者的β-珠蛋白基因的相同片段进行了比较。在所观察到的两个核苷酸差异中,一个产生了一个多态性HinfI位点,该位点存在于地中海贫血β-珠蛋白基因中β-珠蛋白基因上游990bp处,而在正常基因中不存在。然而,另一个具有与上述病例相同分子缺陷的地中海贫血β-珠蛋白基因却没有这个HinfI位点。因此,尚不清楚这个HinfI位点在地中海贫血的产前诊断中是否有任何价值。

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