Nakamichi N, Rhoads D D, Hayashi J I, Kagawa Y, Matsumura T
Meinyu Branch, Research Institute of Innovative Technology for the Earth (RITE) and Laboratory of Cell Technology, Meiji Cell Technology Center, Meiji Milk Products Company, Naruda, 540, Odawara 250, Japan.
J Biochem. 1998 Mar;123(3):392-8. doi: 10.1093/oxfordjournals.jbchem.a021950.
The mitochondrial regulatory region (mrr) located between the tRNAPhe and tRNAPro genes of mitochondrial DNA (mtDNA) is essential for regulation of replication and transcription of the mitochondrial genome. Polyadenylated short RNAs complementary to the L-strand of the mrr in human cells and similar RNAs (polyadenylation status unknown) in rat and mouse cells have been reported. We now report detection of ca. 0.2 kb polyadenylated mrrRNAs in cultured cells of Chinese hamster, African green monkey, mouse, rat, and human. We isolated a cDNA clone to a rat polyadenylated mrrRNA of 158 bp in length excluding the polyadenyl tail, which spans the region from the light strand promoter (LSP) to the origin of heavy strand replication (OriH). This cDNA contains both an open reading frame encoding a 26 amino acid polypeptide and a 12 nucleotide sequence complementary to the 3'-terminus of rat mitochondrial 12S rRNA. A cDNA clone to a human HeLa cell polyadenylated mrrRNA also contains a 12 nucleotide region complementary to the human mitochondrial 12S rRNA. We used a mitochondrial genome-deficient HeLa cell line, rho0 HeLa, and a derived cybrid cell line, HeEB, with a reconstituted mitochondrial genome, to demonstrate that the occurrence of the mrrRNA is dependent on the presence of a mitochondrial genome, and these polyadenylated mrrRNAs are transcribed from the mitochondrial genome. Our results further substantiate the common existence of polyadenylated mrrRNAs among mammals and support previously proposed hypotheses for the multi-functional nature of polyadenylated mrrRNA.
线粒体DNA(mtDNA)中位于tRNAPhe和tRNAPro基因之间的线粒体调控区(mrr)对于线粒体基因组的复制和转录调控至关重要。据报道,在人类细胞中存在与mrr的L链互补的多聚腺苷酸化短RNA,在大鼠和小鼠细胞中也存在类似的RNA(多聚腺苷酸化状态未知)。我们现在报告在中国仓鼠、非洲绿猴、小鼠、大鼠和人类的培养细胞中检测到约0.2 kb的多聚腺苷酸化mrrRNA。我们分离出一个大鼠多聚腺苷酸化mrrRNA的cDNA克隆,其长度为158 bp(不包括多聚腺苷酸尾),跨越从轻链启动子(LSP)到重链复制起点(OriH)的区域。该cDNA既包含一个编码26个氨基酸多肽的开放阅读框,又包含一个与大鼠线粒体12S rRNA 3'末端互补的12个核苷酸序列。人类HeLa细胞多聚腺苷酸化mrrRNA的一个cDNA克隆也包含一个与人类线粒体12S rRNA互补的12个核苷酸区域。我们使用线粒体基因组缺陷的HeLa细胞系rho0 HeLa和一个具有重组线粒体基因组的衍生细胞杂交系HeEB,来证明mrrRNA的出现依赖于线粒体基因组的存在,并且这些多聚腺苷酸化mrrRNA是从线粒体基因组转录而来的。我们的结果进一步证实了多聚腺苷酸化mrrRNA在哺乳动物中普遍存在,并支持了先前提出的关于多聚腺苷酸化mrrRNA多功能性质的假说。