Allmang C, Tollervey D
Institute of Cell and Molecular Biology, University of Edinburgh, Edinburgh, EH9 3JR, United Kingdom.
J Mol Biol. 1998 Apr 24;278(1):67-78. doi: 10.1006/jmbi.1998.1693.
We have undertaken a deletion analysis of the 3' external transcribed spacer (3' ETS) in the pre-rRNA of Saccharomyces cerevisiae. A stem loop structure immediately 3' to the 25 S rRNA region is necessary and sufficient for processing of the 3' ETS. This is believed to be by cotranscriptional cleavage by Rnt1p, the yeast homologue of RNase III. In addition, this stem-loop is required for cleavage of site A3 by RNase MRP and for processing at site B1L, in the 3' region of ITS1. Processing at an upstream site in ITS1, site A2, and at sites in the 5' external transcribed spacer are not affected, even by complete deletion of the 3' ETS. We conclude that processing in the 3' ETS and in ITS1 is coupled. This would constitute a quality control that prevents synthesis of the 5. 8 S rRNA and 5' end maturation of the 25 S rRNA in transcripts which are incomplete due to premature transcription termination.
我们对酿酒酵母前体核糖体RNA(pre-rRNA)中的3'外部转录间隔区(3' ETS)进行了缺失分析。25 S rRNA区域紧挨着3'端的一个茎环结构对于3' ETS的加工是必需且充分的。据信这是通过Rnt1p(核糖核酸酶III的酵母同源物)的共转录切割来实现的。此外,这个茎环对于核糖核酸酶MRP切割A3位点以及ITS1 3'区域中B1L位点的加工是必需的。ITS1中上游的A2位点以及5'外部转录间隔区中的位点的加工不受影响,即使3' ETS完全缺失也是如此。我们得出结论,3' ETS和ITS1中的加工是相互关联的。这将构成一种质量控制机制,防止在由于过早转录终止而不完整的转录本中合成5.8 S rRNA以及25 S rRNA的5'端成熟。