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U8小核仁RNA 5'端的序列对于5.8S和28S核糖体RNA的成熟至关重要。

The sequence of the 5' end of the U8 small nucleolar RNA is critical for 5.8S and 28S rRNA maturation.

作者信息

Peculis B A

机构信息

Genetics and Biochemistry Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-1766, USA.

出版信息

Mol Cell Biol. 1997 Jul;17(7):3702-13. doi: 10.1128/MCB.17.7.3702.

Abstract

Ribosome biogenesis in eucaryotes involves many small nucleolar ribonucleoprotein particles (snoRNP), a few of which are essential for processing pre-rRNA. Previously, U8 snoRNA was shown to play a critical role in pre-rRNA processing, being essential for accumulation of mature 28S and 5.8S rRNAs. Here, evidence which identifies a functional site of interaction on the U8 RNA is presented. RNAs with mutations, insertions, or deletions within the 5'-most 15 nucleotides of U8 do not function in pre-rRNA processing. In vivo competitions in Xenopus oocytes with 2'O-methyl oligoribonucleotides have confirmed this region as a functional site of a base-pairing interaction. Cross-species hybrid molecules of U8 RNA show that this region of the U8 snoRNP is necessary for processing of pre-rRNA but not sufficient to direct efficient cleavage of the pre-rRNA substrate; the structure or proteins comprising, or recruited by, the U8 snoRNP modulate the efficiency of cleavage. Intriguingly, these 15 nucleotides have the potential to base pair with the 5' end of 28S rRNA in a region where, in the mature ribosome, the 5' end of 28S interacts with the 3' end of 5.8S. The 28S-5.8S interaction is evolutionarily conserved and critical for pre-rRNA processing in Xenopus laevis. Taken together these data strongly suggest that the 5' end of U8 RNA has the potential to bind pre-rRNA and in so doing, may regulate or alter the pre-rRNA folding pathway. The rest of the U8 particle may then facilitate cleavage or recruitment of other factors which are essential for pre-rRNA processing.

摘要

真核生物中的核糖体生物合成涉及许多小核仁核糖核蛋白颗粒(snoRNP),其中一些对于前体rRNA的加工至关重要。此前,U8 snoRNA已被证明在前体rRNA加工中起关键作用,对于成熟28S和5.8S rRNA的积累必不可少。本文提供了确定U8 RNA上功能性相互作用位点的证据。在U8最5'端15个核苷酸内有突变、插入或缺失的RNA在前体rRNA加工中不起作用。在非洲爪蟾卵母细胞中与2'-O-甲基寡核糖核苷酸进行的体内竞争已证实该区域是碱基配对相互作用的功能位点。U8 RNA的跨物种杂交分子表明,U8 snoRNP的该区域对于前体rRNA的加工是必需的,但不足以直接有效地切割前体rRNA底物;构成U8 snoRNP或由其招募的结构或蛋白质调节切割效率。有趣的是,这15个核苷酸有可能在成熟核糖体中28S的5'端与5.8S的3'端相互作用的区域与28S rRNA的5'端碱基配对。28S - 5.8S相互作用在进化上是保守的,对非洲爪蟾前体rRNA的加工至关重要。综合这些数据强烈表明,U8 RNA的5'端有可能结合前体rRNA,这样做可能会调节或改变前体rRNA的折叠途径。然后U8颗粒的其余部分可能促进切割或招募前体rRNA加工所必需的其他因子。

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