Li J M, Hopper A K, Martin N C
Department of Biochemistry, School of Medicine, University of Louisville, Kentucky 40292.
J Cell Biol. 1989 Oct;109(4 Pt 1):1411-9. doi: 10.1083/jcb.109.4.1411.
The TRM1 gene of Saccharomyces cerevisiae encodes a tRNA modification enzyme, N2,N2-dimethylguanosine-specific tRNA methyltransferase, which modifies both mitochondrial and cytoplasmic tRNAs. The enzyme is targeted to mitochondria for the modification of mitochondrial tRNAs. Cellular fractionation and indirect immunofluorescence studies reported here demonstrate that this enzyme is also localized to the nucleus. Further, immunofluorescence experiments using strains that overproduce the enzyme show a staining at the periphery of the nucleus suggesting that the enzyme is found in a subnuclear destination near or at the nuclear membrane. There is no obvious cytoplasmic staining in these overproducing strains. Fusion protein technology was used to begin to localize sequences involved in the nuclear targeting of this enzyme. Indirect immunofluorescence studies indicate that sequences between the first 70 and 213 NH2-terminal amino acids of the methyltransferase are sufficient to target Escherichia coli beta-galactosidase to nuclei.
酿酒酵母的TRM1基因编码一种tRNA修饰酶,即N2,N2-二甲基鸟苷特异性tRNA甲基转移酶,它可修饰线粒体和细胞质中的tRNA。该酶定位于线粒体,用于修饰线粒体tRNA。本文报道的细胞分级分离和间接免疫荧光研究表明,这种酶也定位于细胞核。此外,使用过量表达该酶的菌株进行的免疫荧光实验显示,在细胞核周边有染色,这表明该酶存在于靠近核膜或核膜处的亚核位置。在这些过量表达的菌株中没有明显的细胞质染色。融合蛋白技术被用于开始定位该酶核靶向所涉及的序列。间接免疫荧光研究表明,甲基转移酶前70至213个NH2末端氨基酸之间的序列足以将大肠杆菌β-半乳糖苷酶靶向细胞核。