Schmitt M E, Bennett J L, Dairaghi D J, Clayton D A
Department of Developmental Biology, Stanford University School of Medicine, California 94305-5427.
FASEB J. 1993 Jan;7(1):208-13. doi: 10.1096/fasebj.7.1.7678563.
RNase MRP is a ribonucleoprotein endoribonuclease that has been shown to cleave mitochondrial primer RNA sequences from a variety of sources. The bulk of RNase MRP activity is found in the nucleus where its function remains unknown. Two different approaches have resulted in predictions of distinct secondary structures for RNase MRP RNA. In order to analyze more definitively the higher-order structure of RNase MRP RNA, we have conducted a phylogenetic comparison of the available RNase MRP RNA sequences from human, mouse, rat, cow, toad, and yeast. The resulting secondary structure shares features in common with previously described structures for prokaryotic and eukaryotic RNase P RNAs (1) and RNase MRP RNAs (2, 3). In addition, the phylogenetic structure is consistent with available chemical modification data on RNase MRP RNA and with the detailed analysis of the To antigen binding domain located near the 5' end of the RNase MRP RNA. The structure is not limited to RNase MRP RNAs, but can be expanded to cover both eukaryotic RNase P RNAs and RNase P/MRP RNAs from plants.
核糖核酸酶MRP是一种核糖核蛋白内切核糖核酸酶,已被证明能从多种来源切割线粒体引物RNA序列。核糖核酸酶MRP的大部分活性存在于细胞核中,其功能尚不清楚。两种不同的方法得出了核糖核酸酶MRP RNA不同二级结构的预测结果。为了更确切地分析核糖核酸酶MRP RNA的高级结构,我们对来自人类、小鼠、大鼠、牛、蟾蜍和酵母的现有核糖核酸酶MRP RNA序列进行了系统发育比较。所得的二级结构与先前描述的原核和真核核糖核酸酶P RNA(1)以及核糖核酸酶MRP RNA(2,3)的结构具有共同特征。此外,系统发育结构与核糖核酸酶MRP RNA的现有化学修饰数据以及对位于核糖核酸酶MRP RNA 5'端附近的To抗原结合域的详细分析一致。该结构不仅限于核糖核酸酶MRP RNA,还可扩展到涵盖真核核糖核酸酶P RNA和来自植物的核糖核酸酶P/MRP RNA。