Suppr超能文献

真核生物中铁代谢的调节

Regulation of iron metabolism in eukaryotes.

作者信息

Rouault T, Klausner R

机构信息

Cell Biology and Metabolism National Institutes of Child and Human Disease, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Curr Top Cell Regul. 1997;35:1-19. doi: 10.1016/s0070-2137(97)80001-5.

Abstract

Iron metabolism is regulated in cells to ensure that iron supplies are adequate and nontoxic. The expression of iron metabolism is regulated primarily by posttranscriptional mechanisms. Ferritin, eALAS, SDHb of Drosophila, and mammalian mitochondrial aconitase are translationally regulated. The TfR is regulated at the level of mRNA stability. Iron regulatory proteins are regulated either by assembly or by disassembly of an iron-sulfur cluster (IRP1) or by rapid degradation in the presence of iron (IRP2). The list of targets for IRP-mediated regulation is growing longer, and a range of possibilities for versatile regulation exists, as each IRP can bind to unique targets that differ from the consensus IRE. The reactivity of iron with oxygen and the creation of toxic by-products may be the evolutionary stimulus that produced this system of tight posttranscriptional gene regulation.

摘要

细胞中的铁代谢受到调控,以确保铁供应充足且无毒。铁代谢的表达主要受转录后机制调控。铁蛋白、eALAS、果蝇的SDHb和哺乳动物线粒体乌头酸酶受翻译调控。转铁蛋白受体(TfR)在mRNA稳定性水平上受到调控。铁调节蛋白要么通过铁硫簇的组装或拆卸(IRP1)进行调控,要么在铁存在的情况下通过快速降解(IRP2)进行调控。IRP介导的调控靶点列表越来越长,并且存在多种调控可能性,因为每个IRP都可以结合不同于共有铁反应元件(IRE)的独特靶点。铁与氧的反应性以及有毒副产物的产生可能是产生这种严格转录后基因调控系统的进化刺激因素。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验