Li H D, Zagorski J, Fournier M J
Department of Biochemistry, Lederle Graduate Research Center, University of Massachusetts, Amherst 01003.
Mol Cell Biol. 1990 Mar;10(3):1145-52. doi: 10.1128/mcb.10.3.1145-1152.1990.
Repression of an essential nucleolar small nuclear RNA (snRNA) gene of Saccharomyces cerevisiae was shown to result in impaired production of 18S rRNA. The effect, observed for an snRNA species of 128 nucleotides (snR128), was evident within one generation after the onset of SNR128 gene repression and correlated well with depletion of the snRNA. The steady-state mass ratio of 18S RNA to 25S RNA decreased eightfold over the course of the analysis. Results from pulse-chase assays revealed the basis of the imbalance to be underaccumulation of 18S RNA and its 20S precursor. This effect appears to result from impairment of processing of the 35S rRNA transcript at sites that define the 20S species coupled with rapid turnover of unstable intermediates. Possible bases for the effects observed are discussed. A common U14 designation is proposed for the structurally related yeast snRNA and 4.5S hybRNAs from amphibians and mammals.
酿酒酵母一个必需的核仁小核RNA(snRNA)基因的抑制被证明会导致18S rRNA产生受损。对于一种128个核苷酸的snRNA(snR128)观察到的这种效应,在SNR128基因抑制开始后的一代内就很明显,并且与该snRNA的耗竭密切相关。在分析过程中,18S RNA与25S RNA的稳态质量比下降了八倍。脉冲追踪分析结果表明,这种失衡的基础是18S RNA及其20S前体的积累不足。这种效应似乎是由于35S rRNA转录本在定义20S种类的位点处加工受损,以及不稳定中间体的快速周转所致。讨论了观察到这些效应的可能原因。对于来自两栖动物和哺乳动物的结构相关的酵母snRNA和4.5S杂交RNA,提出了一个通用的U14命名。