Cargando…

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,...

Descripción completa

Detalles Bibliográficos
Autores principales: Thomas, Amarni L., Marsman, Judith, Antony, Jisha, Schierding, William, O’Sullivan, Justin M., Horsfield, Julia A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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
_version_ 1783744076411043840
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
work_keys_str_mv AT thomasamarnil transcriptionalregulationofrunx1aninformaticsanalysis
AT marsmanjudith transcriptionalregulationofrunx1aninformaticsanalysis
AT antonyjisha transcriptionalregulationofrunx1aninformaticsanalysis
AT schierdingwilliam transcriptionalregulationofrunx1aninformaticsanalysis
AT osullivanjustinm transcriptionalregulationofrunx1aninformaticsanalysis
AT horsfieldjuliaa transcriptionalregulationofrunx1aninformaticsanalysis