Functional annotation of human long noncoding RNAs via molecular phenotyping
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
- University of Trieste
- University of Toronto
- National University of Singapore
- University of Edinburgh
- Aalborg University
- Imperial College London
- Hiroshima University
- Barcelona Institute of Science and Technology (BIST)
- University of Cape Town
- McGill University
- University of Birmingham
- Stanford University
- ETH Zurich
- Johns Hopkins University
- Weizmann Institute of Science
- IRCCS Fondazione Santa Lucia - Roma
- German Center for Neurodegenerative Diseases (DZNE)
- Osaka University
Abstract
Long noncoding RNAs (lncRNAs) constitute the majority of transcripts in the mammalian genomes, and yet, their functions remain largely unknown. As part of the FANTOM6 project, we systematically knocked down the expression of 285 lncRNAs in human dermal fibroblasts and quantified cellular growth, morphological changes, and transcriptomic responses using Capped Analysis of Gene Expression (CAGE). Antisense oligonucleotides targeting the same lncRNAs exhibited global concordance, and the molecular phenotype, measured by CAGE, recapitulated the observed cellular phenotypes while providing additional insights on the affected genes and pathways. Here, we disseminate the largest-todate lncRNA knockdown data set with molecular phenotyping (over 1000 CAGE deep-sequencing libraries) for further exploration and highlight functional roles for ZNF213-AS1 and lnc-KHDC3L-2.
Details
Original language | English |
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Pages (from-to) | 1060-1072 |
Number of pages | 13 |
Journal | Genome Research |
Volume | 30 |
Issue number | 7 |
Early online date | 27 Jul 2020 |
Publication status | Published - 27 Jul 2020 |
Peer-reviewed | Yes |
External IDs
PubMed | 32718982 |
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