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人类α-珠蛋白基因。重复基因的蛋白质产物是相同的。

The human alpha-globin gene. The protein products of the duplicated genes are identical.

作者信息

Földi J, Cohen-Solal M, Valentin C, Blouquit Y, Hollán S R, Rosa J

出版信息

Eur J Biochem. 1980 Aug;109(2):463-70. doi: 10.1111/j.1432-1033.1980.tb04816.x.

Abstract

In order to determine whether any heterogeneity exists in the human alpha-globin chain, i.e. whether the products of the duplicated genes are identical, we have determined the total sequence of 14 alpha-globin chains: seven of these were abnormal, while six were normal chains from the same individuals, with one additional sample which consisted of the alpha chains from a normal control. In the individuals heterozygous for an alpha-chain abnormality, the product of a single alpha-gene could be isolated from that of the three others using the differing physicochemical properties of the mutant haemoglobins. In the special situation of a double heterozygosity for an alpha-chain abnormality, the products of the two mutated genes were separated from each other and from the mixture of the products of the two normal genes. They were then investigated independently, this approach increased the precision of our work. During the course of the present investigation, sequence determinations were mainly performed on large fragments of the chains, which were purified exclusively by gel chromatography. In this way mixtures of products of several genes could be studied, thereby overcoming the risk of losing peptides differing slightly in sequence. Such loss may often occur when using ion-exchange procedures to purify small peptides. Our results show the absence of any heterogeneity at the level of the gene products of the duplicated alpha loci. Thus the human alpha-globin chain has to be considered as homogeneous.

摘要

为了确定人类α-珠蛋白链中是否存在任何异质性,即重复基因的产物是否相同,我们测定了14条α-珠蛋白链的完整序列:其中7条是异常的,6条是来自同一受试者的正常链,另有一个样本由正常对照的α链组成。在α链异常的杂合子个体中,利用突变血红蛋白不同的物理化学性质,可以将单个α基因的产物与其他三个基因的产物分离。在α链异常的双重杂合子这种特殊情况下,两个突变基因的产物相互分离,并与两个正常基因产物的混合物分离。然后对它们进行独立研究,这种方法提高了我们工作的精确度。在本研究过程中,序列测定主要是在通过凝胶色谱法专门纯化的链的大片段上进行的。通过这种方式,可以研究几个基因产物的混合物,从而克服了丢失序列略有差异的肽段的风险。当使用离子交换程序纯化小肽时,这种丢失经常会发生。我们的结果表明,在重复的α基因座的基因产物水平上不存在任何异质性。因此,人类α-珠蛋白链必须被视为是同质的。

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