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酵母5.8S rRNA的3'端是通过核酸外切酶加工机制产生的。

The 3' end of yeast 5.8S rRNA is generated by an exonuclease processing mechanism.

作者信息

Mitchell P, Petfalski E, Tollervey D

机构信息

European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.

出版信息

Genes Dev. 1996 Feb 15;10(4):502-13. doi: 10.1101/gad.10.4.502.

Abstract

Eukaryotic rRNAs (with the exception of 5S rRNA) are synthesized from a contiguous pre-rRNA precursor by a complex series of processing reactions. Final maturation of yeast 5.8S rRNA involves processing of a 3'-extended, 7S precursor that contains approximately 140 nucleotides of the internal transcribed spacer 2 (ITS2) region. In yeast strains carrying the temperature-sensitive (ts) rrp4-1 mutation, 5.8S rRNA species were observed with 3' extensions of variable length extending up to the 3' end of the 7S pre-rRNA. These 3'-extended 5.8S rRNA species were observed at low levels in rrp4-1 strains under conditions permissive for growth and increased in abundance upon transfer to the nonpermissive temperature. The RRP4 gene was cloned by complementation of the ts growth phenotype of rrp4-1 strains. RRP4 encodes an essential protein of 39-kD predicted molecular mass. Immunoprecipitated Rrp4p exhibited a 3'-->5' exoribonuclease activity in vitro that required RNA with a 3'-terminal hydroxyl group and released nucleoside 5' monophosphates. We conclude that the 7S pre-rRNA is processed to 5.8S rRNA by a 3'-->5' exonuclease activity involving Rrp4p. Homologs of Rrp4p are found in both humans and fission yeast Schizosaccharomyces pombe (43% and 52% identity, respectively), suggesting that the mechanism of 5.8S rRNA 3' end formation has been conserved throughout eukaryotes.

摘要

真核生物的核糖体RNA(5S rRNA除外)是通过一系列复杂的加工反应从一个连续的前体rRNA前体合成而来。酵母5.8S rRNA的最终成熟涉及对一个3'端延伸的7S前体的加工,该前体包含约140个核苷酸的内部转录间隔区2(ITS2)区域。在携带温度敏感型(ts)rrp4-1突变的酵母菌株中,观察到5.8S rRNA种类具有可变长度的3'端延伸,一直延伸到7S前体rRNA的3'端。这些3'端延伸的5.8S rRNA种类在rrp4-1菌株中,在允许生长的条件下水平较低,而在转移到非允许温度后丰度增加。通过互补rrp4-1菌株的ts生长表型克隆了RRP4基因。RRP4编码一种预测分子量为39-kD的必需蛋白质。免疫沉淀的Rrp4p在体外表现出3'→5'外切核糖核酸酶活性,该活性需要具有3'端羟基的RNA并释放5'单磷酸核苷。我们得出结论,7S前体rRNA通过涉及Rrp4p的3'→5'外切核糖核酸酶活性加工成5.8S rRNA。在人类和裂殖酵母粟酒裂殖酵母中都发现了Rrp4p的同源物(分别具有43%和52%的同一性),这表明5.8S rRNA 3'端形成的机制在整个真核生物中是保守的。

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