Frontali L, Palleschi C, Francisci S
Nucleic Acids Res. 1982 Nov 25;10(22):7283-93. doi: 10.1093/nar/10.22.7283.
The transcription of a group of tRNA genes from the large tRNA gene cluster of mitochondrial DNA from Saccharomyces cerevisiae has been investigated by hybridization with DNA probes carrying tRNA coding sequences and small portions of the A + T rich intergenic regions. Results have shown that in some rho- mutants (DS502, F11) mature tRNA was absent, but a few transcripts could be detected. Some high molecular weight species actually hybridized with DNA probes carrying different tRNA coding sequences. Low molecular weight transcripts (100-150 nucleotides, carrying one tRNA sequence) were also present in these mutants. A high molecular weight transcript was also observed in the wild type, though in much more limited amount. The low molecular weight transcripts were analysed by the S1 mapping technique and found to include both a tRNA sequence and the upstream 5' flanking region extending as far as the 3' end of the preceding tRNA gene. The results suggest the existence of a common transcript bearing several tRNA sequences and indicate a possible mechanism of processing, which might be defective in mutants.
通过与携带tRNA编码序列和富含A + T的基因间区域小片段的DNA探针杂交,对酿酒酵母线粒体DNA的大tRNA基因簇中一组tRNA基因的转录进行了研究。结果表明,在一些ρ-突变体(DS502、F11)中,没有成熟的tRNA,但可以检测到一些转录本。一些高分子量的物种实际上与携带不同tRNA编码序列的DNA探针杂交。这些突变体中也存在低分子量转录本(100 - 150个核苷酸,携带一个tRNA序列)。在野生型中也观察到了高分子量转录本,不过数量要少得多。通过S1作图技术分析低分子量转录本,发现其既包含一个tRNA序列,还包括上游5'侧翼区域,该区域一直延伸到前一个tRNA基因的3'端。结果表明存在一种携带多个tRNA序列的共同转录本,并提示了一种可能的加工机制,而这种机制在突变体中可能存在缺陷。