Hinas Andrea, Larsson Pontus, Avesson Lotta, Kirsebom Leif A, Virtanen Anders, Söderbom Fredrik
Department of Molecular Biology, Biomedical Center, Swedish University of Agricultural Sciences, Box 590, SE-75124 Uppsala, Sweden.
Eukaryot Cell. 2006 Jun;5(6):924-34. doi: 10.1128/EC.00065-06.
Most eukaryotic mRNAs depend upon precise removal of introns by the spliceosome, a complex of RNAs and proteins. Splicing of pre-mRNA is known to take place in Dictyostelium discoideum, and we previously isolated the U2 spliceosomal RNA experimentally. In this study, we identified the remaining major spliceosomal RNAs in Dictyostelium by a bioinformatical approach. Expression was verified from 17 small nuclear RNA (snRNA) genes. All these genes are preceded by a putative noncoding RNA gene promoter. Immunoprecipitation showed that snRNAs U1, U2, U4, and U5, but not U6, carry the conserved trimethylated 5' cap structure. A number of divergent U2 species are expressed in Dictyostelium. These RNAs carry the U2 RNA hallmark sequence and structure motifs but have an additional predicted stem-loop structure at the 5' end. Surprisingly, and in contrast to the other spliceosomal RNAs in this study, the new U2 variants were enriched in the cytoplasm and were developmentally regulated. Furthermore, all of the snRNAs could also be detected as polyadenylated species, and polyadenylated U1 RNA was demonstrated to be located in the cytoplasm.
大多数真核生物的信使核糖核酸(mRNA)依赖于剪接体精确去除内含子,剪接体是一种由RNA和蛋白质组成的复合物。已知在盘基网柄菌中会发生前体信使核糖核酸(pre-mRNA)的剪接,我们之前通过实验分离出了U2剪接体RNA。在本研究中,我们通过生物信息学方法鉴定了盘基网柄菌中其余主要的剪接体RNA。从17个小核RNA(snRNA)基因中验证了其表达。所有这些基因之前都有一个假定的非编码RNA基因启动子。免疫沉淀显示,snRNAs U1、U2、U4和U5带有保守的三甲基化5'帽结构,而U6没有。盘基网柄菌中表达了许多不同的U2种类。这些RNA带有U2 RNA标志性序列和结构基序,但在5'端有一个额外预测的茎环结构。令人惊讶的是,与本研究中的其他剪接体RNA不同,新的U2变体在细胞质中富集且受到发育调控。此外,所有的snRNAs也都能被检测为聚腺苷酸化形式,并且已证明聚腺苷酸化的U1 RNA位于细胞质中。