Annotation of nuclear lncRNAs based on chromatin interactions

Author:

Agrawal SaumyaORCID,Buyan Andrey,Severin Jessica,Koido MasaruORCID,Alam TanvirORCID,Abugessaisa Imad,Chang Howard Y.,Dostie Josée,Itoh MasayoshiORCID,Kere JuhaORCID,Kondo Naoto,Li Yunjing,Makeev Vsevolod J.ORCID,Mendez MickaëlORCID,Okazaki Yasushi,Ramilowski Jordan A.,Sigorskikh Andrey I.,Strug Lisa J.,Yagi Ken,Yasuzawa Kayoko,Yip Chi Wai,Hon Chung Chau,Hoffman Michael M.ORCID,Terao ChikashiORCID,Kulakovskiy Ivan V.ORCID,Kasukawa Takeya,Shin Jay W.,Carninci Piero,de Hoon Michiel J. L.ORCID

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.

Funder

Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan

Natural Sciences and Engineering Research Council of Canada

Ministry of Science and Higher Education of the Russian Federation

Publisher

Public Library of Science (PLoS)

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