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Transcriptional Regulation of RUNX1: An Informatics Analysis
The RUNX1/AML1 gene encodes a developmental transcription factor that is an important regulator of haematopoiesis in vertebrates. Genetic disruptions to the RUNX1 gene are frequently associated with acute myeloid leukaemia. Gene regulatory elements (REs), such as enhancers located in non-coding DNA,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395016/ https://www.ncbi.nlm.nih.gov/pubmed/34440349 http://dx.doi.org/10.3390/genes12081175 |
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author | Thomas, Amarni L. Marsman, Judith Antony, Jisha Schierding, William O’Sullivan, Justin M. Horsfield, Julia A. |
author_facet | Thomas, Amarni L. Marsman, Judith Antony, Jisha Schierding, William O’Sullivan, Justin M. Horsfield, Julia A. |
author_sort | Thomas, Amarni L. |
collection | PubMed |
description | The RUNX1/AML1 gene encodes a developmental transcription factor that is an important regulator of haematopoiesis in vertebrates. Genetic disruptions to the RUNX1 gene are frequently associated with acute myeloid leukaemia. Gene regulatory elements (REs), such as enhancers located in non-coding DNA, are likely to be important for Runx1 transcription. Non-coding elements that modulate Runx1 expression have been investigated over several decades, but how and when these REs function remains poorly understood. Here we used bioinformatic methods and functional data to characterise the regulatory landscape of vertebrate Runx1. We identified REs that are conserved between human and mouse, many of which produce enhancer RNAs in diverse tissues. Genome-wide association studies detected single nucleotide polymorphisms in REs, some of which correlate with gene expression quantitative trait loci in tissues in which the RE is active. Our analyses also suggest that REs can be variant in haematological malignancies. In summary, our analysis identifies features of the RUNX1 regulatory landscape that are likely to be important for the regulation of this gene in normal and malignant haematopoiesis. |
format | Online Article Text |
id | pubmed-8395016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83950162021-08-28 Transcriptional Regulation of RUNX1: An Informatics Analysis Thomas, Amarni L. Marsman, Judith Antony, Jisha Schierding, William O’Sullivan, Justin M. Horsfield, Julia A. Genes (Basel) Article The RUNX1/AML1 gene encodes a developmental transcription factor that is an important regulator of haematopoiesis in vertebrates. Genetic disruptions to the RUNX1 gene are frequently associated with acute myeloid leukaemia. Gene regulatory elements (REs), such as enhancers located in non-coding DNA, are likely to be important for Runx1 transcription. Non-coding elements that modulate Runx1 expression have been investigated over several decades, but how and when these REs function remains poorly understood. Here we used bioinformatic methods and functional data to characterise the regulatory landscape of vertebrate Runx1. We identified REs that are conserved between human and mouse, many of which produce enhancer RNAs in diverse tissues. Genome-wide association studies detected single nucleotide polymorphisms in REs, some of which correlate with gene expression quantitative trait loci in tissues in which the RE is active. Our analyses also suggest that REs can be variant in haematological malignancies. In summary, our analysis identifies features of the RUNX1 regulatory landscape that are likely to be important for the regulation of this gene in normal and malignant haematopoiesis. MDPI 2021-07-29 /pmc/articles/PMC8395016/ /pubmed/34440349 http://dx.doi.org/10.3390/genes12081175 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Thomas, Amarni L. Marsman, Judith Antony, Jisha Schierding, William O’Sullivan, Justin M. Horsfield, Julia A. Transcriptional Regulation of RUNX1: An Informatics Analysis |
title | Transcriptional Regulation of RUNX1: An Informatics Analysis |
title_full | Transcriptional Regulation of RUNX1: An Informatics Analysis |
title_fullStr | Transcriptional Regulation of RUNX1: An Informatics Analysis |
title_full_unstemmed | Transcriptional Regulation of RUNX1: An Informatics Analysis |
title_short | Transcriptional Regulation of RUNX1: An Informatics Analysis |
title_sort | transcriptional regulation of runx1: an informatics analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395016/ https://www.ncbi.nlm.nih.gov/pubmed/34440349 http://dx.doi.org/10.3390/genes12081175 |
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