Montoya J, Gaines G L, Attardi G
Cell. 1983 Aug;34(1):151-9. doi: 10.1016/0092-8674(83)90145-9.
A detailed analysis of the mapping and kinetic properties of oligo(dT)-cellulose bound and unbound transcripts synthesized in HeLa cells has indicated that two distinct transcription events take place in the rDNA region. Of these, one appears to start approximately 25 bp upstream of the tRNAPhe gene and to terminate at or near the 3' end of the 16S rRNA gene, being responsible for the synthesis of the bulk of rRNA. The other transcription event starts near the 5' end of the 12S rRNA gene, proceeds beyond the 3' end of the 16S rRNA gene, and results in the synthesis of a polycistronic molecule corresponding to almost the entire H-strand, which is destined to be processed to yield the mRNAs and most of the tRNAs encoded in the heavy strand. The existence of two overlapping transcription units with distinct promoters is probably the basis for the differential regulation of synthesis of the rRNAs and heavy-strand-coded mRNAs.
对在HeLa细胞中合成的与寡聚(dT)-纤维素结合和未结合的转录本的图谱和动力学特性进行的详细分析表明,在rDNA区域发生了两种不同的转录事件。其中之一似乎在tRNAPhe基因上游约25 bp处开始,并在16S rRNA基因的3'末端或其附近终止,负责大部分rRNA的合成。另一个转录事件在12S rRNA基因的5'末端附近开始,延伸至16S rRNA基因的3'末端之外,并导致合成一个几乎对应于整个H链的多顺反子分子,该分子注定要被加工以产生重链中编码的mRNA和大部分tRNA。具有不同启动子的两个重叠转录单元的存在可能是rRNA和重链编码mRNA合成差异调节的基础。