Annotation of nuclear lncRNAs based on chromatin interactions

  • Saumya Agrawal
  • , Andrey Buyan
  • , Jessica Severin
  • , Masaru Koido
  • , Tanvir Alam
  • , Imad Abugessaisa
  • , Howard Y. Chang
  • , Josee Dostie
  • , Masayoshi Itoh
  • , Juha Kere
  • , Naoto Kondo
  • , Yunjing Li
  • , Vsevolod J. Makeev
  • , Mickael Mendez
  • , Yasushi Okazaki
  • , Jordan A. Ramilowski
  • , Andrey I. Sigorskikh
  • , Lisa J. Strug
  • , Ken Yagi
  • , Kayoko Yasuzawa
  • Chi Wai Yip, Chung Chau Hon, Michael M. Hoffman, Chikashi Terao, Ivan V. Kulakovskiy, Takeya Kasukawa, Jay W. Shin, Piero Carninci, Michiel J. L. de Hoon

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

The human genome is pervasively transcribed and produces a wide variety of long non-coding RNAs (lncRNAs), constituting the majority of transcripts across human cell types. Some specific nuclear lncRNAs have been shown to be important regulatory components acting locally. As RNA-chromatin interaction and Hi-C chromatin conformation data showed that chromatin interactions of nuclear lncRNAs are determined by the local chromatin 3D conformation, we used Hi-C data to identify potential target genes of lncRNAs. RNA-protein interaction data suggested that nuclear lncRNAs act as scaffolds to recruit regulatory proteins to target promoters and enhancers. Nuclear lncRNAs may therefore play a role in directing regulatory factors to locations spatially close to the lncRNA gene. We provide the analysis results through an interactive visualization web portal at https://fantom.gsc.riken.jp/zenbu/reports/#F6_3D_lncRNA.
Original languageEnglish
Article numbere0295971
Number of pages24
JournalPLoS ONE
Volume19
Issue number5
DOIs
Publication statusPublished - 6 May 2024

Keywords

  • Long noncoding rnas
  • Set enrichment analysis
  • Susceptibility loci
  • Gene-expression
  • Transcription
  • Reveals
  • Binding
  • Database
  • Architecture
  • Genomics

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