Hughes J M, Ares M
Sinsheimer Laboratories, University of California, Santa Cruz 95064.
EMBO J. 1991 Dec;10(13):4231-9. doi: 10.1002/j.1460-2075.1991.tb05001.x.
Multiple processing events are required to convert a single eukaryotic pre-ribosomal RNA (pre-rRNA) into mature 18S (small subunit), 5.8S and 25-28S (large subunit) rRNAs. We have asked whether U3 small nucleolar RNA is required for pre-rRNA processing in vivo by depleting Saccharomyces cerevisiae of U3 by conditional repression of U3 synthesis. The resulting pattern of accumulation and depletion of specific pre-rRNAs indicates that U3 is required for multiple events leading to the maturation of 18S rRNA. These include an initial cleavage within the 5' external transcribed spacer, resembling the U3 dependent initial processing event of mammalian pre-rRNA. Formation of large subunit rRNAs is unaffected by U3 depletion. The similarity between the effects of U3 depletion and depletion of U14 small nucleolar RNA and the nucleolar protein fibrillarin (NOP1) suggests that these could be components of a single highly conserved processing complex.
要将单个真核生物前核糖体RNA(pre-rRNA)转化为成熟的18S(小亚基)、5.8S和25 - 28S(大亚基)rRNA,需要多个加工事件。我们通过条件性抑制U3合成来耗尽酿酒酵母中的U3,从而研究U3小核仁RNA在体内pre-rRNA加工过程中是否是必需的。特定pre-rRNA积累和耗尽的结果模式表明,U3是导致18S rRNA成熟的多个事件所必需的。这些事件包括5'外部转录间隔区内的初始切割,类似于哺乳动物pre-rRNA的U3依赖性初始加工事件。大亚基rRNA的形成不受U3耗尽的影响。U3耗尽与U14小核仁RNA和核仁蛋白纤维蛋白原(NOP1)耗尽的影响之间的相似性表明,这些可能是单个高度保守加工复合体的组成部分。