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人类中的一种融合基因:宫田血红蛋白异常珠蛋白基因的DNA序列分析

A fusion gene in man: DNA sequence analysis of the abnormal globin gene of hemoglobin Miyada.

作者信息

Kimura A, Ohta Y, Fukumaki Y, Takagi Y

出版信息

Biochem Biophys Res Commun. 1984 Mar 30;119(3):968-74. doi: 10.1016/0006-291x(84)90868-4.

Abstract

An abnormal globin gene from a patient heterozygous for Hemoglobin Miyada was cloned and sequenced. The results indicated that the 5' flanking region and the 5' side of the gene were identical to those of a beta-globin gene and that the 3' side was identical to that of a delta-globin gene. The part of the gene identical to a beta-globin gene shifted to the part identical to the delta-globin gene somewhere in a homologous sequence region between the third nucleotide of the 17th codon and the second nucleotide of the 22nd codon of these two genes. Thus, results of analysis of the nucleotide sequence support the idea that the abnormal globin gene of Hemoglobin Miyada was generated as a fusion gene by unequal crossing over between a beta- and a delta-globin gene.

摘要

对一名血红蛋白宫田杂合子患者的异常珠蛋白基因进行了克隆和测序。结果表明,该基因的5'侧翼区域和基因的5'端与β-珠蛋白基因的相应区域相同,而3'端与δ-珠蛋白基因的相同。该基因中与β-珠蛋白基因相同的部分在这两个基因第17密码子的第三个核苷酸和第22密码子的第二个核苷酸之间的同源序列区域的某处,转移到了与δ-珠蛋白基因相同的部分。因此,核苷酸序列分析结果支持这样一种观点,即血红蛋白宫田的异常珠蛋白基因是由β-珠蛋白基因和δ-珠蛋白基因之间的不等交换产生的融合基因。

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