Functional annotation of human long noncoding RNAs via molecular phenotyping

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • RIKEN
  • Università degli Studi di Trieste
  • RAS - Engelhardt Institute of Molecular Biology
  • RAS - Institute of Protein Research
  • University of Toronto
  • National University of Singapore
  • University of Edinburgh
  • Aalborg University
  • Imperial College London
  • Medical Research Council (MRC)
  • Max-Delbrück-Centrum für Molekulare Medizin (MDC)
  • Russian Academy of Sciences
  • 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
  • Deutsches Zentrum für Neurodegenerative Erkrankungen e.V. (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

OriginalspracheEnglisch
Seiten (von - bis)1060-1072
Seitenumfang13
FachzeitschriftGenome Research
Jahrgang30
Ausgabenummer7
Frühes Online-Datum27 Juli 2020
PublikationsstatusVeröffentlicht - 27 Juli 2020
Peer-Review-StatusJa

Externe IDs

PubMed 32718982

Schlagworte

ASJC Scopus Sachgebiete