Atzorn Vera, Fragapane Paola, Kiss Tamás
Laboratoire de Biologie Moléculaire Eucaryote du CNRS, UMR5099, IFR109 CNRS, Université Paul Sabatier, 31062 Toulouse Cedex, France.
Mol Cell Biol. 2004 Feb;24(4):1769-78. doi: 10.1128/MCB.24.4.1769-1778.2004.
Saccharomyces cerevisiae snR30 is an essential box H/ACA small nucleolar RNA (snoRNA) required for the processing of 18S rRNA. Here, we show that the previously characterized human, reptilian, amphibian, and fish U17 snoRNAs represent the vertebrate homologues of yeast snR30. We also demonstrate that U17/snR30 is present in the fission yeast Schizosaccharomyces pombe and the unicellular ciliated protozoan Tetrahymena thermophila. Evolutionary comparison revealed that the 3'-terminal hairpins of U17/snR30 snoRNAs contain two highly conserved sequence motifs, the m1 (AUAUUCCUA) and m2 (AAACCAU) elements. Mutation analysis of yeast snR30 demonstrated that the m1 and m2 elements are essential for early cleavages of the 35S pre-rRNA and, consequently, for the production of mature 18S rRNA. The m1 and m2 motifs occupy the opposite strands of an internal loop structure, and they are located invariantly 7 nucleotides upstream from the ACA box of U17/snR30 snoRNAs. U17/snR30 is the first identified box H/ACA snoRNA that possesses an evolutionarily conserved role in the nucleolytic processing of eukaryotic pre-rRNA.
酿酒酵母snR30是一种对于18S rRNA加工至关重要的盒式H/ACA小核仁RNA(snoRNA)。在此,我们表明先前已鉴定的人类、爬行类、两栖类和鱼类的U17 snoRNAs代表酵母snR30的脊椎动物同源物。我们还证明U17/snR30存在于裂殖酵母粟酒裂殖酵母和单细胞纤毛原生动物嗜热栖热四膜虫中。进化比较显示,U17/snR30 snoRNAs的3'末端发夹结构包含两个高度保守的序列基序,即m1(AUAUUCCUA)和m2(AAACCAU)元件。酵母snR30的突变分析表明,m1和m2元件对于35S前体rRNA的早期切割至关重要,因此对于成熟18S rRNA的产生也至关重要。m1和m2基序占据内部环结构的相反链,并且它们始终位于U17/snR30 snoRNAs的ACA盒上游7个核苷酸处。U17/snR30是首个被鉴定出在真核生物前体rRNA的核酸酶加工中具有进化保守作用的盒式H/ACA snoRNA。