Peculis B A, Greer C L
National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Genetics and Biochemistry Branch, Bethesda, Maryland 20892, USA.
RNA. 1998 Dec;4(12):1610-22. doi: 10.1017/s1355838298981420.
Accurate and efficient processing of pre-rRNA is critical to the accumulation of mature functional ribosomal subunits for maintenance of cell growth. Processing requires numerous factors which act in trans as well as RNA sequence/ structural elements which function in cis. To examine the latter, we have used directed mutagenesis and expression of mutated pre-rRNAs in yeast. Specifically, we tested requirements for formation of an ITS2-proximal stem on processing, a structure formed by an interaction between sequences corresponding to the 3' end of 5.8S rRNA and the 5' end of 25S. Pre-rRNA processing is inhibited in templates encoding mutations that prevent the formation of the ITS2-proximal stem. Compensatory, double mutations, which alter the sequence of this region but restore the structure of the stem, also restore processing, although at lower efficiency. This reduction in efficiency is reflected in decreased levels of mature 5.8S and 25S rRNA and increased levels of 35S pre-rRNA and certain processing intermediates. This phenotype is reminiscent of the biochemical depletion of U8 snoRNA in vertebrates for which the ITS2-proximal stem has been proposed as a potential site for interaction with U8 RNP. Thus, formation of the ITS2-proximal stem may be a requirement common to yeast and vertebrate pre-rRNA processing.
前体核糖体RNA(pre-rRNA)的准确高效加工对于积累成熟的功能性核糖体亚基以维持细胞生长至关重要。加工过程需要众多反式作用因子以及顺式作用的RNA序列/结构元件。为了研究后者,我们在酵母中使用了定点诱变和突变前体rRNA的表达。具体而言,我们测试了加工过程中ITS2近端茎环形成的要求,该结构由对应于5.8S rRNA 3'端和25S 5'端的序列相互作用形成。在编码阻止ITS2近端茎环形成的突变的模板中,前体rRNA加工受到抑制。补偿性双突变改变了该区域的序列,但恢复了茎环结构,也能恢复加工,尽管效率较低。效率的降低表现为成熟的5.8S和25S rRNA水平下降,以及35S前体rRNA和某些加工中间体水平升高。这种表型让人联想到脊椎动物中U8小核仁RNA(snoRNA)的生化缺失,其ITS2近端茎环被认为是与U8核糖核蛋白(RNP)相互作用的潜在位点。因此,ITS2近端茎环的形成可能是酵母和脊椎动物前体rRNA加工的共同要求。