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论文摘要

PRPS1基因及其突变与相关临床综合征的研究进展

Research progress of PRPS1 gene and its mutations and related clinical syndrome

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Author:

收稿日期:2019-12-11          年卷(期)页码:2020,43(01):82-88

期刊名称:国际输血及血液学杂志

Journal Name:International Journal of Blood Transfusion and Hematology

关键字:磷酸核糖焦磷酸,综合征,代谢,磷酸核糖焦磷酸合成酶,PRPS1基因

Key words:Phosphoribosyl pyrophosphate|Syndrome|Metabolism|Phosphoribosyl pyrophosphate synthetase|PRPS1 gene

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中文摘要

英文摘要

Phosphoribosyl pyrophosphate synthetase (PRS) 1, encoded by PRPS1 gene, is the first limiting enzyme participating in the synthetic process of nucleic acids. Consequently, it has a great effect on cell functions, especially the synthesis and metabolism of purine and pyrimidine. Some changes in PRS1 crystal structure might exert inconceivable effects on enzyme activity and lead to disorder of purine/pyrimidine metabolism, even cellular energy metabolism failure. Inherited mutation may induce disfunction of some energy-intensive tissue, the common clinical manifestations are some clinical syndrome. In addition, PRPS1 mutations found in cancer are proved to be an important cause of tumor resistance, followed by patient relapse. In a word, PRS1 plays a key role in energy metabolism, signal transduction and nucleic acid synthesis, which is of great significance in maintaining physiological activities. This article mainly focuses on the physiological functions and crystal structure of PRS1, the regulation of cell metabolism by PRPS1 gene and its mutations, as well as clinical syndromes related to PRPS1 gene mutation.

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