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从酵母到人——肯尼迪途径在磷脂酰胆碱合成中的作用。

From yeast to humans - roles of the Kennedy pathway for phosphatidylcholine synthesis.

机构信息

Department of Pharmacology, Dalhousie University, Halifax, Canada.

出版信息

FEBS Lett. 2018 Apr;592(8):1256-1272. doi: 10.1002/1873-3468.12919. Epub 2017 Dec 19.

Abstract

The major phospholipid present in most eukaryotic membranes is phosphatidylcholine (PC), comprising ~ 50% of phospholipid content. PC metabolic pathways are highly conserved from yeast to humans. The main pathway for the synthesis of PC is the Kennedy (CDP-choline) pathway. In this pathway, choline is converted to phosphocholine by choline kinase, phosphocholine is metabolized to CDP-choline by the rate-determining enzyme for this pathway, CTP:phosphocholine cytidylyltransferase, and cholinephosphotransferase condenses CDP-choline with diacylglycerol to produce PC. This Review discusses how PC synthesis via the Kennedy pathway is regulated, its role in cellular and biological processes, as well as diseases known to be associated with defects in PC synthesis. Finally, we present the first model for the making of a membrane via PC synthesis.

摘要

在大多数真核生物膜中存在的主要磷脂是磷脂酰胆碱(PC),约占磷脂含量的 50%。从酵母到人,PC 的代谢途径高度保守。PC 的主要合成途径是肯尼狄(CDP-胆碱)途径。在该途径中,胆碱激酶将胆碱转化为磷酸胆碱,限速酶 CTP:磷酸胆碱胞苷转移酶将磷酸胆碱代谢为 CDP-胆碱,然后胆碱磷酸转移酶将 CDP-胆碱与二酰基甘油缩合生成 PC。本综述讨论了通过肯尼狄途径合成 PC 的调控机制,其在细胞和生物学过程中的作用,以及与 PC 合成缺陷相关的已知疾病。最后,我们提出了通过 PC 合成制造膜的第一个模型。

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