Kretzner L, Krol A, Rosbash M
Howard Hughes Medical Institute, Waltham, MA.
Proc Natl Acad Sci U S A. 1990 Jan;87(2):851-5. doi: 10.1073/pnas.87.2.851.
The five small nuclear RNAs (snRNAs) involved in mammalian pre-mRNA splicing (U1, U2, U4, U5, and U6) are well conserved in length, sequence, and especially secondary structure. These five snRNAs from Saccharomyces cerevisiae show notable size and sequence differences from their metazoan counterparts. This is most striking for the large S. cerevisiae U1 and U2 snRNAs, for which no secondary structure models currently exist. Because of the importance of U1 snRNA in the early steps of "spliceosome" assembly, we wanted to compare the highly conserved secondary structure of metazoan U1 snRNA (approximately 165 nucleotides) with that of S. cerevisiae U1 snRNA (568 nucleotides). To this end, we have cloned and sequenced the U1 gene from two other yeast species possessing large U1 RNAs. Using computer-derived structure predictions, phylogenetic comparisons, and structure probing, we have arrived at a secondary structure model for S. cerevisiae U1 snRNA. The results show that most elements of higher eukaryotic U1 snRNA secondary structure are conserved in S. cerevisiae. The hundreds of "extra" nucleotides of yeast U1 RNA, also highly structured, suggest that large insertions and/or deletions have occurred during the evolution of the U1 gene.
参与哺乳动物前体mRNA剪接的五种小核RNA(snRNA,即U1、U2、U4、U5和U6)在长度、序列,尤其是二级结构方面高度保守。酿酒酵母的这五种snRNA与其后生动物对应物相比,在大小和序列上存在显著差异。这在酿酒酵母较大的U1和U2 snRNA中最为明显,目前尚无它们的二级结构模型。由于U1 snRNA在“剪接体”组装的早期步骤中很重要,我们希望比较后生动物U1 snRNA(约165个核苷酸)与酿酒酵母U1 snRNA(568个核苷酸)高度保守的二级结构。为此,我们从另外两种拥有大型U1 RNA的酵母物种中克隆并测序了U1基因。通过计算机推导的结构预测、系统发育比较和结构探测,我们得出了酿酒酵母U1 snRNA的二级结构模型。结果表明酿酒酵母中高等真核生物U1 snRNA二级结构的大多数元件是保守的。酵母U1 RNA数百个“额外”的核苷酸也具有高度结构化,这表明在U1基因的进化过程中发生了大量的插入和/或缺失。