Suppr超能文献

斑马鱼作为嘧啶核苷酸代谢紊乱研究模型。

Zebrafish as a model for study of disorders in pyrimidine nucleotide metabolism.

机构信息

Department of Anatomy, Physiology and Biochemistry, The Swedish University of Agricultural Sciences, Uppsala, Sweden.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2024;43(8):722-733. doi: 10.1080/15257770.2023.2298742. Epub 2023 Dec 28.

Abstract

Pyrimidine nucleotides are not only the building blocks of DNA and RNA but also participate in multiple cellular metabolic processes, including protein, lipid and polysaccharide biosynthesis. Pyrimidine nucleotides are synthesized by two distinct pathways-the and salvage pathways. Disorders in pyrimidine nucleotide metabolism cause severe neurodegenerative disorders in human. For example, deficiency in thymidylate kinase, an essential enzyme in dTTP synthesis, causes severe microcephaly in human patients. Zebrafish mutants selected by insertion mutagenesis that results in inactive enzymes in pyrimidine metabolism showed also neurological and developmental disorders. In this work I have summarized current data on neurological and developmental disorders caused by defects in enzymes in pyrimidine nucleotide metabolism in zebrafish and compared to human. All these data suggest that zebrafish is a useful animal model to study pathogenic mechanism of neurological disorders due to defect in pyrimidine nucleotide metabolism.

摘要

嘧啶核苷酸不仅是 DNA 和 RNA 的构建模块,还参与多种细胞代谢过程,包括蛋白质、脂质和多糖的生物合成。嘧啶核苷酸由两条不同的途径合成——从头合成途径和补救途径。嘧啶核苷酸代谢紊乱会导致人类严重的神经退行性疾病。例如,胸苷酸激酶的缺乏,这是 dTTP 合成中的一种必需酶,会导致人类患者严重的小头畸形。通过插入诱变选择的斑马鱼突变体,导致嘧啶代谢中酶的失活,也表现出神经和发育障碍。在这项工作中,我总结了目前关于斑马鱼中嘧啶核苷酸代谢酶缺陷引起的神经和发育障碍的研究数据,并与人类进行了比较。所有这些数据表明,斑马鱼是研究由于嘧啶核苷酸代谢缺陷导致的神经疾病发病机制的有用动物模型。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验