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Chromatin occupancy and target genes of the haematopoietic master transcription factor MYB
The 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 com...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076236/ https://www.ncbi.nlm.nih.gov/pubmed/33903675 http://dx.doi.org/10.1038/s41598-021-88516-w |
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author | Lemma, Roza B. Ledsaak, Marit Fuglerud, Bettina M. Sandve, Geir Kjetil Eskeland, Ragnhild Gabrielsen, Odd S. |
author_facet | Lemma, Roza B. Ledsaak, Marit Fuglerud, Bettina M. Sandve, Geir Kjetil Eskeland, Ragnhild Gabrielsen, Odd S. |
author_sort | Lemma, Roza B. |
collection | PubMed |
description | The 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. |
format | Online Article Text |
id | pubmed-8076236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80762362021-04-27 Chromatin occupancy and target genes of the haematopoietic master transcription factor MYB Lemma, Roza B. Ledsaak, Marit Fuglerud, Bettina M. Sandve, Geir Kjetil Eskeland, Ragnhild Gabrielsen, Odd S. Sci Rep Article The 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. Nature Publishing Group UK 2021-04-26 /pmc/articles/PMC8076236/ /pubmed/33903675 http://dx.doi.org/10.1038/s41598-021-88516-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lemma, Roza B. Ledsaak, Marit Fuglerud, Bettina M. Sandve, Geir Kjetil Eskeland, Ragnhild Gabrielsen, Odd S. Chromatin occupancy and target genes of the haematopoietic master transcription factor MYB |
title | Chromatin occupancy and target genes of the haematopoietic master transcription factor MYB |
title_full | Chromatin occupancy and target genes of the haematopoietic master transcription factor MYB |
title_fullStr | Chromatin occupancy and target genes of the haematopoietic master transcription factor MYB |
title_full_unstemmed | Chromatin occupancy and target genes of the haematopoietic master transcription factor MYB |
title_short | Chromatin occupancy and target genes of the haematopoietic master transcription factor MYB |
title_sort | chromatin occupancy and target genes of the haematopoietic master transcription factor myb |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8076236/ https://www.ncbi.nlm.nih.gov/pubmed/33903675 http://dx.doi.org/10.1038/s41598-021-88516-w |
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