Gunisova Stanislava, Elboher Elhanan, Nosek Jozef, Gorkovoy Valentin, Brown Yogev, Lucier Jean-Francois, Laterreur Nancy, Wellinger Raymund J, Tzfati Yehuda, Tomaska Lubomir
Department of Genetics, Comenius University, Bratislava, Slovak Republic.
RNA. 2009 Apr;15(4):546-59. doi: 10.1261/rna.1194009. Epub 2009 Feb 17.
The RNA component of telomerase (telomerase RNA; TER) varies substantially both in sequence composition and size (from approximately 150 nucleotides [nt] to >1500 nt) across species. This dramatic divergence has hampered the identification of TER genes and a large-scale comparative analysis of TER sequences and structures among distantly related species. To identify by phylogenetic analysis conserved sequences and structural features of TER that are of general importance, it is essential to obtain TER sequences from evolutionarily distant groups of species, providing enough conservation within each group and enough variation among the groups. To this end, we identified TER genes in several yeast species with relatively large (>20 base pairs) and nonvariant telomeric repeats, mostly from the genus Candida. Interestingly, several of the TERs reported here are longer than all other yeast TERs known to date. Within these TERs, we predicted a pseudoknot containing U-A.U base triples (conserved in vertebrates, budding yeasts, and ciliates) and a three-way junction element (conserved in vertebrates and budding yeasts). In addition, we identified a novel conserved sequence (CS2a) predicted to reside within an internal-loop structure, in all the budding yeast TERs examined. CS2a is located near the Est1p-binding bulge-stem previously identified in Saccharomyces cerevisiae. Mutational analyses in both budding yeasts S. cerevisiae and Kluyveromyces lactis demonstrate that CS2a is essential for in vivo telomerase function. The comparative and mutational analyses of conserved TER elements reported here provide novel insights into the structure and function of the telomerase ribonucleoprotein complex.
端粒酶的RNA组分(端粒酶RNA;TER)在序列组成和大小上(从大约150个核苷酸[nt]到>1500 nt)在不同物种间差异很大。这种显著的差异阻碍了TER基因的鉴定以及远缘物种间TER序列和结构的大规模比较分析。为了通过系统发育分析鉴定TER中具有普遍重要性的保守序列和结构特征,从进化上距离较远的物种组中获取TER序列至关重要,每个组内要有足够的保守性且组间要有足够的变异性。为此,我们在几个具有相对较大(>20个碱基对)且不变异的端粒重复序列的酵母物种中鉴定了TER基因,这些物种大多来自假丝酵母属。有趣的是,这里报道的几个TER比迄今已知的所有其他酵母TER都长。在这些TER中,我们预测了一个包含U - A·U碱基三联体(在脊椎动物、芽殖酵母和纤毛虫中保守)的假结和一个三向连接元件(在脊椎动物和芽殖酵母中保守)。此外,在所有检测的芽殖酵母TER中,我们鉴定了一个预计位于内环结构内的新保守序列(CS2a)。CS2a位于先前在酿酒酵母中鉴定出的Est1p结合凸起 - 茎附近。在芽殖酵母酿酒酵母和乳酸克鲁维酵母中的突变分析表明,CS2a对于体内端粒酶功能至关重要。这里报道的保守TER元件的比较和突变分析为端粒酶核糖核蛋白复合物的结构和功能提供了新的见解。