Ramamonjisoa D, Kauffmann S, Choisne N, Maréchal-Drouard L, Green G, Wintz H, Small I, Dietrich A
Institut de Biologie Moléculaire des Plantes, UPR A0406 du CNRS, Université Louis Pasteur, Strasbourg, France.
Plant Mol Biol. 1998 Mar;36(4):613-25. doi: 10.1023/a:1005972023506.
Bean nuclear genes for tRNA(Pro), tRNA(Thr) and tRNA(Leu) were isolated. Expression of the tRNA(Pro) genes was demonstrated in vivo and sequence analysis suggested amplification of the tRNA(Pro) gene copy number through duplication of a gene cluster at the same locus of the bean genome. The two tRNA(Thr) genes isolated were actively transcribed and their transcripts processed in a HeLa cell system. In vivo expression tests of these genes and aminoacylation assays of the corresponding in vitro transcripts showed the presence of identity determinants in the anticodon of plant tRNA(Thr). The tRNA(Leu) gene was not expressed due to deviation from the consensus in the internal B-box promoter. The same sequence deviation also prevented aminoacylation of the corresponding in vitro transcript. This tRNA(Leu) however exists in plants and is synthesized from another gene with a consensus B-box promoter. Plant mitochondria import from the cytosol a number of nucleus-encoded tRNAs, including tRNA(Leu) and tRNA(Thr). From the available sequence data, we could not identify any conserved structural motif characteristic for the nucleus-encoded tRNAs imported into plant mitochondria, either in the tRNAs, or in the gene flanking sequences. These results suggest that recognition of tRNAs for import is idiosyncratic and likely to depend on protein/RNA interactions that are specific to each tRNA or each isoacceptor group.
分离出了豆类中编码tRNA(Pro)、tRNA(Thr)和tRNA(Leu)的核基因。在体内证实了tRNA(Pro)基因的表达,序列分析表明,通过豆类基因组同一基因座处基因簇的重复,tRNA(Pro)基因拷贝数得以扩增。分离出的两个tRNA(Thr)基因在HeLa细胞系统中被积极转录并对其转录本进行了加工。这些基因的体内表达测试以及相应体外转录本的氨酰化测定表明,植物tRNA(Thr)的反密码子中存在身份决定因素。由于内部B盒启动子与共有序列存在偏差,tRNA(Leu)基因未表达。同样的序列偏差也阻止了相应体外转录本的氨酰化。然而,这种tRNA(Leu)存在于植物中,是由另一个具有共有B盒启动子的基因合成的。植物线粒体从细胞质中导入许多核编码的tRNA,包括tRNA(Leu)和tRNA(Thr)。根据现有的序列数据,我们无法在tRNA或基因侧翼序列中识别出导入植物线粒体的核编码tRNA所特有的任何保守结构基序。这些结果表明,tRNA导入的识别是特异的,可能取决于每个tRNA或每个同功受体组特有的蛋白质/RNA相互作用。