基因技术、胰岛素基因表征及其与糖尿病的关系研究。

Endokrinologie Pub Date : 1982-06-01
D Schröder, H Zühlke
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引用次数: 0

摘要

现代分子生物学方法的发展和引入是胰岛素基因表征的先决条件。人类胰岛素A和B链的化学合成基因以及自然存在的大鼠胰岛素基因转移到细菌中,为在细菌系统中产生胰岛素提供了可能性。测定了大鼠I型和大鼠II型胰岛素基因以及人胰岛素基因的结构。对从人类染色体基因库中分离的人类胰岛素基因进行结构分析,鉴定出单个人类胰岛素基因的等位变异。人类胰岛素基因位于11号染色体的短臂上。胰岛素结构异常与糖尿病的发生发展有关的假说可以在临床实践中得到证实。从糖尿病患者分离的人胰岛素显示氨基酸序列异常和激素生物活性降低。这一发现表明,在某些糖尿病病例中,由于胰岛素基因突变导致的结构异常胰岛素的合成可能是导致相对胰岛素缺乏和高血糖的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gene technology, characterization of insulin gene and the relationship to diabetes research.

The development and introduction of modern molecular biological methods was a prerequisite to the characterization of the insulin gene. The transfer of chemically synthesized genes for human insulin A and B chains as well as the naturally occurring rat insulin gene into bacteria opened possibilities to produce insulin in bacterial systems. Moreover, the structure of rat I and rat II insulin genes as well as human insulin gene were determined. Structural analysis of human insulin genes isolated from a human chromosomal gene library led to the identification of allelic variants of a single human insulin gene. The human insulin gene is located on the short arm of chromosome 11. The hypothesis that structurally abnormal insulin could play a role in the development of diabetes mellitus could be proved in clinical practice. Human insulin isolated from a diabetic patient showed an abnormality in the amino acid sequence and a decreased biological activity of the hormone. This finding demonstrates that in certain cases of diabetes mellitus the synthesis of structurally abnormal insulin due to a mutation in the insulin gene can be the cause for the development of relative insulin deficiency and hyperglycaemia.

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