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缺氧对铁调节蛋白 1 表达的影响及其机制。

Effect of hypoxia on the expression of iron regulatory proteins 1 and the mechanisms involved.

机构信息

Department of Biochemistry, Institute of Nautical Medicine, Nantong University, Nantong 226001, People's Republic of China.

出版信息

IUBMB Life. 2011 Feb;63(2):120-8. doi: 10.1002/iub.419.

Abstract

Iron is essential for many biological processes, including oxygen delivery, and its supply is tightly regulated. Iron regulatory proteins (IRPs, IRP1 and IRP2) are master regulators of cellular iron metabolism. Hypoxia triggers a broad range of gene responses that are primarily mediated by hypoxia-inducible factor-1 (HIF-1). In this study, we have shown that hypoxia could not only upregulate the expression of hypoxia inducible factor-1 but also downregulate the expression of IRP1. However, the molecular mechanisms that govern the IRP1 response to hypoxia are not known. Herein we suggested that HIF/HRE system was an essential link between IRP1 and hypoxia. The HRE of IRP1 5'-regulation regions could combine with HIF-1 in vitro. Dual-luciferase reporter assay showed that IRP1 was directly downregulated by HIF/HRE system.

摘要

铁是许多生物过程所必需的,包括氧气输送,其供应受到严格调节。铁调节蛋白(IRPs,IRP1 和 IRP2)是细胞铁代谢的主要调节剂。缺氧引发广泛的基因反应,主要由缺氧诱导因子-1(HIF-1)介导。在这项研究中,我们已经表明,缺氧不仅可以上调缺氧诱导因子-1 的表达,还可以下调 IRP1 的表达。然而,调节 IRP1 对缺氧反应的分子机制尚不清楚。在这里,我们认为 HIF/HRE 系统是 IRP1 和缺氧之间的重要联系。IRP1 5'-调控区的 HRE 可以在体外与 HIF-1 结合。双荧光素酶报告基因检测显示,IRP1 被 HIF/HRE 系统直接下调。

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