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dc.date.accessioned2021-12-17T18:52:43Z
dc.date.available2021-12-17T18:52:43Z
dc.date.created2021-05-04T10:38:20Z
dc.date.issued2021
dc.identifier.citationLemma, Roza Berhanu Ledsaak, Marit Fuglerud, Bettina Maria Sandve, Geir Kjetil Eskeland, Ragnhild Gabrielsen, Odd Stokke . Chromatin occupancy and target genes of the haematopoietic master transcription factor MYB. Scientific Reports. 2021, 11(9008)
dc.identifier.urihttp://hdl.handle.net/10852/89608
dc.description.abstractThe transcription factor MYB is a master regulator in haematopoietic progenitor cells and a pioneer factor affecting differentiation and proliferation of these cells. Leukaemic transformation may be promoted by high MYB levels. Despite much accumulated molecular knowledge of MYB, we still lack a comprehensive understanding of its target genes and its chromatin action. In the present work, we performed a ChIP-seq analysis of MYB in K562 cells accompanied by detailed bioinformatics analyses. We found that MYB occupies both promoters and enhancers. Five clusters (C1–C5) were found when we classified MYB peaks according to epigenetic profiles. C1 was enriched for promoters and C2 dominated by enhancers. C2-linked genes were connected to hematopoietic specific functions and had GATA factor motifs as second in frequency. C1 had in addition to MYB-motifs a significant frequency of ETS-related motifs. Combining ChIP-seq data with RNA-seq data allowed us to identify direct MYB target genes. We also compared ChIP-seq data with digital genomic footprinting. MYB is occupying nearly a third of the super-enhancers in K562. Finally, we concluded that MYB cooperates with a subset of the other highly expressed TFs in this cell line, as expected for a master regulator
dc.languageEN
dc.publisherNature Portfolio
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleChromatin occupancy and target genes of the haematopoietic master transcription factor MYB
dc.typeJournal article
dc.creator.authorLemma, Roza Berhanu
dc.creator.authorLedsaak, Marit
dc.creator.authorFuglerud, Bettina Maria
dc.creator.authorSandve, Geir Kjetil
dc.creator.authorEskeland, Ragnhild
dc.creator.authorGabrielsen, Odd Stokke
cristin.unitcode185,57,0,0
cristin.unitnameNorsk Senter for Molekylærmedisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1907924
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Scientific Reports&rft.volume=11&rft.spage=&rft.date=2021
dc.identifier.jtitleScientific Reports
dc.identifier.volume11
dc.identifier.issue1
dc.identifier.pagecount18
dc.identifier.doihttps://doi.org/10.1038/s41598-021-88516-w
dc.identifier.urnURN:NBN:no-92222
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2045-2322
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/89608/2/s41598-021-88516-w.pdf
dc.type.versionPublishedVersion
cristin.articleid9008
dc.relation.projectNOTUR/NORSTORE/nn9374k
dc.relation.projectNFR/187615
dc.relation.projectNFR/275783


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