Hentze M W, Seuanez H N, O'Brien S J, Harford J B, Klausner R D
Cell Biology and Metabolism Branch, National Institute of Child Health and Human Development, Bethesda, MD 20892.
Nucleic Acids Res. 1989 Aug 11;17(15):6103-8. doi: 10.1093/nar/17.15.6103.
Three human mRNAs are regulated post-transcriptionally by iron via iron-responsive elements (IREs) contained in each mRNA. A cytoplasmic protein (IRE-BP) binds to these cis-acting elements and mediates the translational regulation of ferritin H- and L-chain mRNA and the iron-dependent stability of transferrin receptor (TfR) mRNA. We have taken advantage of the different mobilities of the human and rodent IRE/IRE-BP complexes on non-denaturing polyacrylamide gels to determine the chromosomal localization of the gene encoding the IRE-BP. Utilizing a panel of 34 different human/rodent hybrid cell lines we have assigned the IRE-BP gene to human chromosome 9. This new technique based on nucleic acid/protein interaction may allow determination of the chromosomal localization of other RNA- or DNA-binding proteins.
三种人类mRNA通过各自mRNA中所含的铁反应元件(IRE)在转录后受到铁的调节。一种细胞质蛋白(IRE-BP)与这些顺式作用元件结合,并介导铁蛋白H链和L链mRNA的翻译调控以及转铁蛋白受体(TfR)mRNA的铁依赖性稳定性。我们利用人类和啮齿动物IRE/IRE-BP复合物在非变性聚丙烯酰胺凝胶上的不同迁移率来确定编码IRE-BP的基因的染色体定位。利用一组34种不同的人类/啮齿动物杂交细胞系,我们已将IRE-BP基因定位于人类9号染色体。这种基于核酸/蛋白质相互作用的新技术可能有助于确定其他RNA或DNA结合蛋白的染色体定位。