Frenkel-Morgenstern Milana, Gorohovski Alessandro, Vucenovic Dunja, Maestre Lorena, Valencia Alfonso
Structural Biology and BioComputing Program, Spanish National Cancer Research Centre (CNIO), Madrid 28029, Spain.
Monoclonal Antibodies Unit, Spanish National Cancer Research Centre (CNIO), Madrid 28029, Spain.
Nucleic Acids Res. 2015 Jan;43(Database issue):D68-75. doi: 10.1093/nar/gku1199. Epub 2014 Nov 20.
Chimeric RNAs that comprise two or more different transcripts have been identified in many cancers and among the Expressed Sequence Tags (ESTs) isolated from different organisms; they might represent functional proteins and produce different disease phenotypes. The ChiTaRS 2.1 database of chimeric transcripts and RNA-Seq data (http://chitars.bioinfo.cnio.es/) is the second version of the ChiTaRS database and includes improvements in content and functionality. Chimeras from eight organisms have been collated including novel sense-antisense (SAS) chimeras resulting from the slippage of the sense and anti-sense intragenic regions. The new database version collects more than 29,000 chimeric transcripts and indicates the expression and tissue specificity for 333 entries confirmed by RNA-seq reads mapping the chimeric junction sites. User interface allows for rapid and easy analysis of evolutionary conservation of fusions, literature references and experimental data supporting fusions in different organisms. More than 1428 cancer breakpoints have been automatically collected from public databases and manually verified to identify their correct cross-references, genomic sequences and junction sites. As a result, the ChiTaRS 2.1 collection of chimeras from eight organisms and human cancer breakpoints extends our understanding of the evolution of chimeric transcripts in eukaryotes as well as their functional role in carcinogenic processes.
在许多癌症以及从不同生物体中分离出的表达序列标签(EST)中,已经鉴定出了由两个或更多不同转录本组成的嵌合RNA;它们可能代表功能性蛋白质并产生不同的疾病表型。嵌合转录本和RNA测序数据的ChiTaRS 2.1数据库(http://chitars.bioinfo.cnio.es/)是ChiTaRS数据库的第二个版本,在内容和功能方面都有所改进。已整理了来自八个生物体的嵌合体,包括由有义链和反义链基因内区域滑动产生的新型有义-反义(SAS)嵌合体。新的数据库版本收集了超过29,000个嵌合转录本,并通过映射嵌合连接位点的RNA测序读数对333个条目的表达和组织特异性进行了标注。用户界面允许快速轻松地分析融合的进化保守性、文献参考以及支持不同生物体中融合的实验数据。已从公共数据库中自动收集了超过1428个癌症断点,并进行了人工验证,以确定其正确的交叉引用、基因组序列和连接位点。因此,来自八个生物体的嵌合体和人类癌症断点的ChiTaRS 2.1集合扩展了我们对真核生物中嵌合转录本进化及其在致癌过程中功能作用的理解。