真核生物铁代谢的调控。

T Rouault, R Klausner
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引用次数: 249

摘要

铁代谢在细胞中受到调节,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的调控。果蝇的铁蛋白、eALAS、SDHb和哺乳动物的线粒体乌头酶受翻译调控。TfR在mRNA稳定性水平上受到调控。铁调节蛋白通过铁硫簇的组装或拆卸(IRP1)或在铁存在下的快速降解(IRP2)来调节。IRP介导的调控靶点越来越多,多种调控的可能性也越来越多,因为每个IRP都可以结合不同于共识IRE的独特靶点。铁与氧的反应性和有毒副产物的产生可能是产生这种严格的转录后基因调控系统的进化刺激。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of iron metabolism in eukaryotes.

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.

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