Vance V B, Thompson E A, Bowman L H
Nucleic Acids Res. 1985 Oct 25;13(20):7499-513. doi: 10.1093/nar/13.20.7499.
Truncated mouse ribosomal DNA (rDNA) genes were stably incorporated into rat HTC-5 cells by DNA-mediated cell transfection techniques. The mouse rDNA genes were accurately transcribed in these rat cells indicating that there is no absolute species specificity of rDNA transcription between mouse and rat. No more than 170 nucleotides of the 5' nontranscribed spacer was required for the accurate initiation of mouse rDNA transcription in rat cells. Further, the mouse transcripts were accurately cleaved at the 5' end of the 18S rRNA sequence, even though these transcripts contained neither the 3' end of mouse 18S rRNA nor any other downstream mouse sequences. Thus, cleavage at the 5' end of 18S rRNA is not dependent on long range interactions involving these downstream sequences.
通过DNA介导的细胞转染技术,截短的小鼠核糖体DNA(rDNA)基因被稳定地整合到大鼠HTC-5细胞中。这些小鼠rDNA基因在这些大鼠细胞中被准确转录,这表明小鼠和大鼠之间rDNA转录不存在绝对的物种特异性。在大鼠细胞中准确起始小鼠rDNA转录,5'非转录间隔区不超过170个核苷酸是必需的。此外,小鼠转录本在18S rRNA序列的5'端被准确切割,尽管这些转录本既不包含小鼠18S rRNA的3'端,也不包含任何其他下游小鼠序列。因此,18S rRNA 5'端的切割不依赖于涉及这些下游序列的长程相互作用。