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Processing of a dicistronic small nucleolar RNA precursor by the RNA endonuclease Rnt1.

机译:RNA内切核酸酶Rnt1处理双顺反子小核仁RNA前体。

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摘要

Small nucleolar RNAs (snoRNAs) are intron encoded or expressed from monocistronic independent transcription units, or, in the case of plants, from polycistronic clusters. We show that the snR190 and U14 snoRNAs from the yeast Saccharomyces cerevisiae are co-transcribed as a dicistronic precursor which is processed by the RNA endonuclease Rnt1, the yeast ortholog of bacterial RNase III. RNT1 disruption results in a dramatic decrease in the levels of mature U14 and snR190 and in accumulation of dicistronic snR190-U14 RNAs. Addition of recombinant Rnt1 to yeast extracts made from RNT1 disruptants induces the chase of dicistronic RNAs into mature snoRNAs, showing that dicistronic RNAs correspond to functional precursors stalled in the processing pathway. Rnt1 cleaves a dicistronic transcript in vitro in the absence of other factors, separating snR190 from U14. Thus, one of the functions of eukaryotic RNase III is, as for the bacterial enzyme, to liberate monocistronic RNAs from polycistronic transcripts.
机译:小核仁RNA(snoRNA)是由单顺反子独立转录单位(或在植物中为多顺反子簇)编码或表达的内含子。我们显示,来自酿酒酵母的snR190和U14 snoRNAs被共转录为双顺反子前体,由RNA内切酶Rnt1(细菌RNase III的酵母直系同源物)处理。 RNT1破坏导致成熟的U14和snR190的水平急剧下降,并导致双顺反子snR190-U14 RNA的积累。向由RNT1破坏物制成的酵母提取物中添加重组Rnt1可以将双顺反子RNA追逐到成熟的snoRNA中,表明双顺反子RNA对应于停滞在加工途径中的功能性前体。在没有其他因素的情况下,Rnt1在体外切割了双顺反子转录物,将snR190与U14分开。因此,就细菌酶而言,真核RNase III的功能之一是从多顺反子转录物中释放出单顺反子RNA。

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