Corral-Debrinski M, Blugeon C, Jacq C
Laboratoire de Génétique Moléculaire, UMR CNRS 8541, Ecole Normale Supérieure, 75230 Paris, France.
Mol Cell Biol. 2000 Nov;20(21):7881-92. doi: 10.1128/MCB.20.21.7881-7892.2000.
We isolated mitochondria from Saccharomyces cerevisiae to selectively study polysomes bound to the mitochondrial surface. The distribution of several mRNAs coding for mitochondrial proteins was examined in free and mitochondrion-bound polysomes. Some mRNAs exclusively localize to mitochondrion-bound polysomes, such as the ones coding for Atm1p, Cox10p, Tim44p, Atp2p, and Cot1p. In contrast, mRNAs encoding Cox6p, Cox5a, Aac1p, and Mir1p are found enriched in free cytoplasmic polysome fractions. Aac1p and Mir1p are transporters that lack cleavable presequences. Sequences required for mRNA asymmetric subcellular distribution were determined by analyzing the localization of reporter mRNAs containing the presequence coding region and/or the 3'-untranslated region (3'UTR) of ATM1, a gene encoding an ABC transporter of the mitochondrial inner membrane. Biochemical analyses of mitochondrion-bound polysomes and direct visualization of RNA localization in living yeast cells allowed us to demonstrate that either the presequence coding region or the 3'UTR of ATM1 is sufficient to allow the reporter mRNA to localize to the vicinity of the mitochondrion, independently of its translation. These data demonstrate that mRNA localization is one of the mechanisms used, in yeast, for segregating mitochondrial proteins.
我们从酿酒酵母中分离出线粒体,以选择性地研究与线粒体表面结合的多核糖体。在游离的和与线粒体结合的多核糖体中检测了几种编码线粒体蛋白的mRNA的分布。一些mRNA仅定位于与线粒体结合的多核糖体,例如编码Atm1p、Cox10p、Tim44p、Atp2p和Cot1p的mRNA。相比之下,编码Cox6p、Cox5a、Aac1p和Mir1p的mRNA在游离的细胞质多核糖体组分中含量丰富。Aac1p和Mir1p是缺乏可切割前导序列的转运蛋白。通过分析含有前导序列编码区和/或线粒体内膜ABC转运蛋白编码基因ATM1的3'-非翻译区(3'UTR)的报告mRNA的定位,确定了mRNA不对称亚细胞分布所需的序列。对与线粒体结合的多核糖体的生化分析以及对活酵母细胞中RNA定位的直接观察使我们能够证明,ATM1的前导序列编码区或3'UTR足以使报告mRNA定位于线粒体附近,而与其翻译无关。这些数据表明,mRNA定位是酵母中用于分离线粒体蛋白的机制之一。