Gurney T
Nucleic Acids Res. 1985 Jul 11;13(13):4905-19. doi: 10.1093/nar/13.13.4905.
Mouse fibroblasts labeled 1-9 h with 3H-uridine contained radioactive 45S rRNA subspecies of 13.9, 13.3, and 12.8 kb, as determined by hybrid-selection with rDNA plasmids and by electrophoresis in agarose-formaldehyde. The 13.9 kb subspecies contained 5' and 3' terminal rDNA sequences known from the work of Grummt and colleagues to be at or near the ends of the primary transcript. The 13.3 kb subspecies contained the 3' terminal sequence but lacked the 5' terminal sequence. The 12.8 kb subspecies lacked both terminal sequences. Washed nuclei produced one discrete species of 13.9 kb. The results suggested that synthesis of the primary transcript terminated 500 +/- 100 nucleotides beyond the 3' end of 28S rRNA, that the first processing cleavage occurred 600 +/- 100 nucleotides from the origin of synthesis, and the second cleavage occurred near the 3' end of 28S rRNA. Changes in relative radioactivities among the subspecies after serum stimulation or after treatment with low concentrations of cycloheximide suggesting that processing was not perfectly coupled with synthesis and that cycloheximide inhibited one cleavage more than others.
用³H-尿苷标记1 - 9小时的小鼠成纤维细胞含有放射性的45S rRNA亚类,其大小分别为13.9、13.3和12.8 kb,这是通过与rDNA质粒进行杂交选择以及在琼脂糖 - 甲醛中电泳确定的。13.9 kb的亚类包含5'和3'末端rDNA序列,根据格鲁姆特及其同事的研究,这些序列位于初级转录本的末端或其附近。13.3 kb的亚类包含3'末端序列,但缺少5'末端序列。12.8 kb的亚类则两个末端序列都没有。洗涤后的细胞核产生一种13.9 kb的离散物种。结果表明,初级转录本的合成在28S rRNA 3'末端下游500±100个核苷酸处终止,第一次加工切割发生在距合成起始点600±100个核苷酸处,第二次切割发生在28S rRNA 3'末端附近。血清刺激或用低浓度环己酰亚胺处理后,亚类之间相对放射性的变化表明加工过程与合成并非完美偶联,且环己酰亚胺对一种切割的抑制作用比对其他切割的抑制作用更强。