Chapple Charles E, Guigó Roderic, Krol Alain
Institut Municipal d'Investigació Mèdica, Universitat Pompeu Fabra and Parc de Recerca Biomedica de Barcelona, Carrer del Doctor Aiguader 88, 08003, Barcelona, Catalonia, Spain.
Bioinformatics. 2009 Mar 1;25(5):674-5. doi: 10.1093/bioinformatics/btp020. Epub 2009 Jan 29.
Selenoproteins contain the 21st amino acid selenocysteine which is encoded by an inframe UGA codon, usually read as a stop. In eukaryotes, its co-translational recoding requires the presence of an RNA stem-loop structure, the SECIS element in the 3 untranslated region of (UTR) selenoprotein mRNAs. Despite little sequence conservation, SECIS elements share the same overall secondary structure. Until recently, the lack of a significantly high number of selenoprotein mRNA sequences hampered the identification of other potential sequence conservation. In this work, the web-based tool SECISaln provides for the first time an extensive structure-based sequence alignment of SECIS elements resulting from the well-defined secondary structure of the SECIS RNA and the increased size of the eukaryotic selenoproteome. We have used SECISaln to improve our knowledge of SECIS secondary structure and to discover novel, conserved nucleotide positions and we believe it will be a useful tool for the selenoprotein and RNA scientific communities.
SECISaln is freely available as a web-based tool at http://genome.crg.es/software/secisaln/.
硒蛋白包含第21种氨基酸硒代半胱氨酸,它由一个框内UGA密码子编码,该密码子通常被读作终止密码子。在真核生物中,其共翻译重编码需要RNA茎环结构的存在,即硒蛋白mRNA 3'非翻译区(UTR)中的硒代半胱氨酸插入序列(SECIS)元件。尽管序列保守性较低,但SECIS元件具有相同的整体二级结构。直到最近,由于缺乏大量的硒蛋白mRNA序列,阻碍了其他潜在序列保守性的鉴定。在这项工作中,基于网络的工具SECISaln首次提供了基于结构的SECIS元件广泛序列比对,这是由SECIS RNA明确的二级结构和真核硒蛋白组规模的增加所实现的。我们使用SECISaln来增进对SECIS二级结构的了解,并发现新的保守核苷酸位置,我们相信它将成为硒蛋白和RNA科学界的一个有用工具。
SECISaln作为基于网络的工具可在http://genome.crg.es/software/secisaln/免费获取。