Recounting the FANTOM CAGE-Associated Transcriptome.
Eddie Luidy ImadaDiego Fernando SanchezLeonardo Collado-TorresChristopher WilksTejasvi MatamWikum DinalankaraAleksey StupnikovFrancisco Pereira LoboChi-Wai YipKayoko YasuzawaNaoto KondoMasayoshi ItohHarukazu SuzukiTakeya KasukawaChung-Chau HonMichiel J L de HoonJay W ShinPiero CarniciAndrew E JaffeJeffery T LeekAlexander V FavorovGloria R FrancoBen LangmeadLuigi MarchionniPublished in: Genome research (2020)
Long noncoding RNAs (lncRNAs) have emerged as key coordinators of biological and cellular processes. Characterizing lncRNA expression across cells and tissues is key to understanding their role in determining phenotypes, including human diseases. We present here FC-R2, a comprehensive expression atlas across a broadly defined human transcriptome, inclusive of over 109,000 coding and noncoding genes, as described in the FANTOM CAGE-Associated Transcriptome (FANTOM-CAT) study. This atlas greatly extends the gene annotation used in the original recount2 resource. We demonstrate the utility of the FC-R2 atlas by reproducing key findings from published large studies and by generating new results across normal and diseased human samples. In particular, we (a) identify tissue-specific transcription profiles for distinct classes of coding and noncoding genes, (b) perform differential expression analysis across thirteen cancer types, identifying novel noncoding genes potentially involved in tumor pathogenesis and progression, and (c) confirm the prognostic value for several enhancer lncRNAs expression in cancer. Our resource is instrumental for the systematic molecular characterization of lncRNA by the FANTOM6 Consortium. In conclusion, comprised of over 70,000 samples, the FC-R2 atlas will empower other researchers to investigate functions and biological roles of both known coding genes and novel lncRNAs.
Keyphrases
- genome wide identification
- genome wide
- single cell
- transcription factor
- endothelial cells
- poor prognosis
- rna seq
- genome wide analysis
- gene expression
- dna methylation
- induced pluripotent stem cells
- papillary thyroid
- long non coding rna
- binding protein
- pluripotent stem cells
- bioinformatics analysis
- induced apoptosis
- systematic review
- squamous cell
- randomized controlled trial
- cell death
- long noncoding rna
- childhood cancer