Dandjinou Alain T, Lévesque Nancy, Larose Stéphanie, Lucier Jean-François, Abou Elela Sherif, Wellinger Raymund J
Groupe ARN/RNA Group, Department of Microbiology and Infectious Diseases, Faculty of Medicine, Université de Sherbrooke, 3001 12th Avenue N., Sherbrooke, QC J1H 5N4, Canada.
Curr Biol. 2004 Jul 13;14(13):1148-58. doi: 10.1016/j.cub.2004.05.054.
Telomerase is a ribonucleoprotein complex whose RNA moiety dictates the addition of specific simple sequences onto chromosomes ends. While relevant for certain human genetic diseases, the contribution of the essential telomerase RNA to RNP assembly still remains unclear. Phylogenetic analyses of vertebrate and ciliate telomerase RNAs revealed conserved elements that potentially organize protein subunits for RNP function. In contrast, the yeast telomerase RNA could not be fitted to any known structural model, and the limited number of known sequences from Saccharomyces species did not permit the prediction of a yeast specific conserved structure.
We cloned and analyzed the complete telomerase RNA loci (TLC1) from all known Saccharomyces species belonging to the "sensu stricto" group. Complementation analyses in S. cerevisiae and end mappings of mature RNAs ensured the relevance of the cloned sequences. By using phylogenetic comparative analysis coupled with in vitro enzymatic probing, we derived a secondary structure prediction of the Saccharomyces cerevisiae TLC1 RNA. This conserved secondary structure prediction includes a central domain that is likely to orchestrate DNA synthesis and at least two accessory domains important for RNA stability and telomerase recruitment. The structure also reveals a potential tertiary interaction between two loops in the central core.
The predicted secondary structure of the TLC1 RNA of S. cerevisiae reveals a distinct folding pattern featuring well-separated but conserved functional elements. The predicted structure now allows for a detailed and rationally designed study to the structure-function relationships within the telomerase RNP-complex in a genetically tractable system.
端粒酶是一种核糖核蛋白复合体,其RNA部分决定了特定简单序列添加到染色体末端。虽然这与某些人类遗传疾病相关,但关键的端粒酶RNA对核糖核蛋白组装的贡献仍不清楚。对脊椎动物和纤毛虫端粒酶RNA的系统发育分析揭示了保守元件,这些元件可能为核糖核蛋白功能组织蛋白质亚基。相比之下,酵母端粒酶RNA无法适配任何已知的结构模型,并且来自酿酒酵母属物种的已知序列数量有限,无法预测酵母特异性的保守结构。
我们克隆并分析了来自“狭义”组所有已知酿酒酵母物种的完整端粒酶RNA基因座(TLC1)。在酿酒酵母中的互补分析和成熟RNA的末端定位确保了克隆序列的相关性。通过使用系统发育比较分析结合体外酶促探测,我们得出了酿酒酵母TLC1 RNA的二级结构预测。这种保守的二级结构预测包括一个可能协调DNA合成的中央结构域和至少两个对RNA稳定性和端粒酶募集很重要的辅助结构域。该结构还揭示了中央核心中两个环之间潜在的三级相互作用。
酿酒酵母TLC1 RNA的预测二级结构揭示了一种独特的折叠模式,其特征是功能元件分离但保守。现在,预测的结构允许在一个遗传上易于处理的系统中对端粒酶核糖核蛋白复合体中的结构-功能关系进行详细且合理设计的研究。