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A DNA Contact Map for the Mouse Runx1 Gene Identifies Novel Haematopoietic Enhancers
The transcription factor Runx1 is essential for definitive haematopoiesis, and the RUNX1 gene is frequently translocated or mutated in leukaemia. Runx1 is transcribed from two promoters, P1 and P2, to give rise to different protein isoforms. Although the expression of Runx1 must be tightly regulated...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645309/ https://www.ncbi.nlm.nih.gov/pubmed/29042628 http://dx.doi.org/10.1038/s41598-017-13748-8 |
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author | Marsman, Judith Thomas, Amarni Osato, Motomi O’Sullivan, Justin M. Horsfield, Julia A. |
author_facet | Marsman, Judith Thomas, Amarni Osato, Motomi O’Sullivan, Justin M. Horsfield, Julia A. |
author_sort | Marsman, Judith |
collection | PubMed |
description | The transcription factor Runx1 is essential for definitive haematopoiesis, and the RUNX1 gene is frequently translocated or mutated in leukaemia. Runx1 is transcribed from two promoters, P1 and P2, to give rise to different protein isoforms. Although the expression of Runx1 must be tightly regulated for normal blood development, the mechanisms that regulate Runx1 isoform expression during haematopoiesis remain poorly understood. Gene regulatory elements located in non-coding DNA are likely to be important for Runx1 transcription. Here we use circular chromosome conformation capture sequencing to identify DNA interactions with the P1 and P2 promoters of Runx1, and the previously identified +24 enhancer, in the mouse multipotent haematopoietic progenitor cell line HPC-7. The active promoter, P1, interacts with nine non-coding regions that are occupied by transcription factors within a 1 Mb topologically associated domain. Eight of nine regions function as blood-specific enhancers in zebrafish, of which two were previously shown to harbour blood-specific enhancer activity in mice. Interestingly, the +24 enhancer interacted with multiple distant regions on chromosome 16, suggesting it may regulate the expression of additional genes. The Runx1 DNA contact map identifies connections with multiple novel and known haematopoietic enhancers that are likely to be involved in regulating Runx1 expression in haematopoietic progenitor cells. |
format | Online Article Text |
id | pubmed-5645309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56453092017-10-26 A DNA Contact Map for the Mouse Runx1 Gene Identifies Novel Haematopoietic Enhancers Marsman, Judith Thomas, Amarni Osato, Motomi O’Sullivan, Justin M. Horsfield, Julia A. Sci Rep Article The transcription factor Runx1 is essential for definitive haematopoiesis, and the RUNX1 gene is frequently translocated or mutated in leukaemia. Runx1 is transcribed from two promoters, P1 and P2, to give rise to different protein isoforms. Although the expression of Runx1 must be tightly regulated for normal blood development, the mechanisms that regulate Runx1 isoform expression during haematopoiesis remain poorly understood. Gene regulatory elements located in non-coding DNA are likely to be important for Runx1 transcription. Here we use circular chromosome conformation capture sequencing to identify DNA interactions with the P1 and P2 promoters of Runx1, and the previously identified +24 enhancer, in the mouse multipotent haematopoietic progenitor cell line HPC-7. The active promoter, P1, interacts with nine non-coding regions that are occupied by transcription factors within a 1 Mb topologically associated domain. Eight of nine regions function as blood-specific enhancers in zebrafish, of which two were previously shown to harbour blood-specific enhancer activity in mice. Interestingly, the +24 enhancer interacted with multiple distant regions on chromosome 16, suggesting it may regulate the expression of additional genes. The Runx1 DNA contact map identifies connections with multiple novel and known haematopoietic enhancers that are likely to be involved in regulating Runx1 expression in haematopoietic progenitor cells. Nature Publishing Group UK 2017-10-17 /pmc/articles/PMC5645309/ /pubmed/29042628 http://dx.doi.org/10.1038/s41598-017-13748-8 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Marsman, Judith Thomas, Amarni Osato, Motomi O’Sullivan, Justin M. Horsfield, Julia A. A DNA Contact Map for the Mouse Runx1 Gene Identifies Novel Haematopoietic Enhancers |
title | A DNA Contact Map for the Mouse Runx1 Gene Identifies Novel Haematopoietic Enhancers |
title_full | A DNA Contact Map for the Mouse Runx1 Gene Identifies Novel Haematopoietic Enhancers |
title_fullStr | A DNA Contact Map for the Mouse Runx1 Gene Identifies Novel Haematopoietic Enhancers |
title_full_unstemmed | A DNA Contact Map for the Mouse Runx1 Gene Identifies Novel Haematopoietic Enhancers |
title_short | A DNA Contact Map for the Mouse Runx1 Gene Identifies Novel Haematopoietic Enhancers |
title_sort | dna contact map for the mouse runx1 gene identifies novel haematopoietic enhancers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645309/ https://www.ncbi.nlm.nih.gov/pubmed/29042628 http://dx.doi.org/10.1038/s41598-017-13748-8 |
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