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Regulating the fate of mRNA: the control of cellular iron metabolism.

作者信息

Klausner R D, Rouault T A, Harford J B

机构信息

Cell Biology and Metabolism Branch National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Cell. 1993 Jan 15;72(1):19-28. doi: 10.1016/0092-8674(93)90046-s.

DOI:10.1016/0092-8674(93)90046-s
PMID:8380757
Abstract
摘要

相似文献

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Regulating the fate of mRNA: the control of cellular iron metabolism.调控mRNA的命运：细胞铁代谢的控制
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2
Cellular iron homeostasis: a paradigm for mechanisms of posttranscriptional control of gene expression.细胞铁稳态：基因表达转录后调控机制的范例
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Intracellular iron metabolism.细胞内铁代谢
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The interaction between the iron-responsive element binding protein and its cognate RNA is highly dependent upon both RNA sequence and structure.铁反应元件结合蛋白与其同源RNA之间的相互作用高度依赖于RNA的序列和结构。
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Molecular control of vertebrate iron metabolism: mRNA-based regulatory circuits operated by iron, nitric oxide, and oxidative stress.脊椎动物铁代谢的分子调控：由铁、一氧化氮和氧化应激操纵的基于mRNA的调控回路。
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7
Iron-dependent regulation of ferritin and transferrin receptor expression by the iron-responsive element binding protein.铁反应元件结合蛋白对铁蛋白和转铁蛋白受体表达的铁依赖性调节
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Cloning of the cDNA encoding an RNA regulatory protein--the human iron-responsive element-binding protein.编码一种RNA调节蛋白——人铁反应元件结合蛋白的cDNA的克隆
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The 5'-untranslated region of human transferrin mRNA, which contains a putative iron-regulatory element, is bound by purified iron-regulatory protein in a sequence-specific manner.人转铁蛋白mRNA的5′非翻译区含有一个假定的铁调节元件，它能被纯化的铁调节蛋白以序列特异性方式结合。
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Annu Rev Nutr. 2000;20:627-62. doi: 10.1146/annurev.nutr.20.1.627.

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