Granick D
J Cell Biol. 1975 May;65(2):398-417. doi: 10.1083/jcb.65.2.398.
A number of chemicals, mostly adenosine analogues, cause the nucleolus of the chick embryo fibroblast to lose material and unravel over a period of several hours into beaded strands termed nucleolar necklaces (NN). The results of analyses of the fibroblasts, treated with the NN-forming chemical dichlororibobenzimidazole (DRB), suggests that the following biochemical alterations occur: DRB almost completely prevents the increase in both messenger RNA (mRNA) and heterogeneous nuclear RNA. It interferes with ribosome synthesis by decreasing the rate of 45S ribosomal RNA (rRNA) accumulation by 50%, slowing the rate of 18S rRNA appearance by 50%, and causing an extensive degradation (80%) of the 32S and 28S rRNA-containing preribisomes. Most of this preribosome degration probably occurs at or before the 32S rRNA preribosome stage. The degradation of these preribosomes appears to be due to the formation of defective 45S rRNA preribosomes rather than to a direct DRB interference with preribosome processing enzyme action. DRB inhibits total cellular RNA synthesis in less than 15 min, suggesting a direct interference with RNA synthesis. DRB also inhibits the uptake of nucleosides into the cell. DRB in the concentrations used does not appear to directly interfere with the translation of mRNA (i.e., protein synthesis). Other NN-forming adenoside analogues and high concentrations of adenosine (2 mM) cause biochemical alterations similar to those produced by DRB. To explain the preribosome degradation, we propose the hypothesis that DRB inhibits the synthesis of mRNA; as a consequence, some of the preribosomal proteins that normally coat the 32S rRNA portion of the 45S precursor RNA become limiting, and this defective portion is then subject to degradation by nucleases.
许多化学物质,主要是腺苷类似物,会导致鸡胚成纤维细胞的核仁在数小时内失去物质并解聚成串珠状链,称为核仁项链(NN)。用形成NN的化学物质二氯核糖苯并咪唑(DRB)处理成纤维细胞的分析结果表明,会发生以下生化改变:DRB几乎完全阻止信使核糖核酸(mRNA)和不均一核RNA的增加。它通过将45S核糖体RNA(rRNA)积累速率降低50%、将18S rRNA出现速率减慢50%以及导致含32S和28S rRNA的前核糖体大量降解(80%)来干扰核糖体合成。这种前核糖体的降解大部分可能发生在32S rRNA前核糖体阶段或之前。这些前核糖体的降解似乎是由于有缺陷的45S rRNA前核糖体的形成,而不是DRB直接干扰前核糖体加工酶的作用。DRB在不到15分钟内抑制总细胞RNA合成,表明对RNA合成有直接干扰。DRB还抑制核苷进入细胞。所用浓度的DRB似乎不会直接干扰mRNA的翻译(即蛋白质合成)。其他形成NN的腺苷类似物和高浓度的腺苷(2 mM)会引起与DRB产生的类似生化改变。为了解释前核糖体的降解,我们提出以下假说:DRB抑制mRNA的合成;因此,一些通常覆盖45S前体RNA的32S rRNA部分的前核糖体蛋白变得有限,然后这个有缺陷的部分会被核酸酶降解。