Di Liegro C M, Bellafiore M, Izquierdo J M, Rantanen A, Cuezva J M
Departamento de Biología Molecular, Centro de Biología Molecular Severo Ochoa, Universidad Autónoma de Madrid, 28049 Madrid, Spain.
Biochem J. 2000 Nov 15;352 Pt 1(Pt 1):109-15.
Recent findings have indicated that the 3'-untranslated region (3'-UTR) of the mRNA encoding the beta-catalytic subunit of the mitochondrial H(+)-ATP synthase has an in vitro translation-enhancing activity (TEA) [Izquierdo and Cuezva, Mol. Cell. Biol. (1997) 17, 5255-5268; Izquierdo and Cuezva, Biochem. J. (2000) 346, 849-855]. In the present work, we have expressed chimaeric plasmids that encode mRNA variants of green fluorescent protein in normal rat kidney and liver clone 9 cells to determine whether the 3'-UTRs of nuclear-encoded mRNAs involved in the biogenesis of mitochondria have an intrinsic TEA. TEA is found in the 3'-UTR of the mRNAs encoding the alpha- and beta-subunits of the rat H(+)-ATP synthase complex, as well as in subunit IV of cytochrome c oxidase. No TEA is present in the 3'-UTR of the somatic mRNA encoding rat mitochondrial transcription factor A. Interestingly, the TEA of the 3'-UTR of mRNAs of oxidative phosphorylation is different, depending upon the cell type analysed. These data provide the first in vivo evidence of a novel cell-specific mechanism for the control of the translation of mRNAs required in mitochondrial function.
最近的研究结果表明,线粒体H(+)-ATP合酶β催化亚基编码mRNA的3'-非翻译区(3'-UTR)具有体外翻译增强活性(TEA)[伊兹基尔多和奎兹瓦,《分子细胞生物学》(1997年)17卷,5255 - 5268页;伊兹基尔多和奎兹瓦,《生物化学杂志》(2000年)346卷,849 - 855页]。在本研究中,我们在正常大鼠肾和肝克隆9细胞中表达了编码绿色荧光蛋白mRNA变体的嵌合质粒,以确定参与线粒体生物合成的核编码mRNA的3'-UTR是否具有内在的TEA。在大鼠H(+)-ATP合酶复合体α和β亚基编码mRNA的3'-UTR中发现了TEA,细胞色素c氧化酶亚基IV中也有。在编码大鼠线粒体转录因子A的体细胞mRNA的3'-UTR中未发现TEA。有趣的是,氧化磷酸化mRNA的3'-UTR的TEA因所分析的细胞类型而异。这些数据首次在体内证明了一种控制线粒体功能所需mRNA翻译的新型细胞特异性机制。