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The Function of the Conserved Regulatory Element within the Second Intron of the Mammalian Csf1r Locus
The gene encoding the receptor for macrophage colony-stimulating factor (CSF-1R) is expressed exclusively in cells of the myeloid lineages as well as trophoblasts. A conserved element in the second intron, Fms-Intronic Regulatory Element (FIRE), is essential for macrophage-specific transcription of...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3561417/ https://www.ncbi.nlm.nih.gov/pubmed/23383005 http://dx.doi.org/10.1371/journal.pone.0054935 |
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author | Sauter, Kristin A. Bouhlel, M. Amine O’Neal, Julie Sester, David P. Tagoh, Hiromi Ingram, Richard M. Pridans, Clare Bonifer, Constanze Hume, David A. |
author_facet | Sauter, Kristin A. Bouhlel, M. Amine O’Neal, Julie Sester, David P. Tagoh, Hiromi Ingram, Richard M. Pridans, Clare Bonifer, Constanze Hume, David A. |
author_sort | Sauter, Kristin A. |
collection | PubMed |
description | The gene encoding the receptor for macrophage colony-stimulating factor (CSF-1R) is expressed exclusively in cells of the myeloid lineages as well as trophoblasts. A conserved element in the second intron, Fms-Intronic Regulatory Element (FIRE), is essential for macrophage-specific transcription of the gene. However, the molecular details of how FIRE activity is regulated and how it impacts the Csf1r promoter have not been characterised. Here we show that agents that down-modulate Csf1r mRNA transcription regulated promoter activity altered the occupancy of key FIRE cis-acting elements including RUNX1, AP1, and Sp1 binding sites. We demonstrate that FIRE acts as an anti-sense promoter in macrophages and reversal of FIRE orientation within its native context greatly reduced enhancer activity in macrophages. Mutation of transcription initiation sites within FIRE also reduced transcription. These results demonstrate that FIRE is an orientation-specific transcribed enhancer element. |
format | Online Article Text |
id | pubmed-3561417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35614172013-02-04 The Function of the Conserved Regulatory Element within the Second Intron of the Mammalian Csf1r Locus Sauter, Kristin A. Bouhlel, M. Amine O’Neal, Julie Sester, David P. Tagoh, Hiromi Ingram, Richard M. Pridans, Clare Bonifer, Constanze Hume, David A. PLoS One Research Article The gene encoding the receptor for macrophage colony-stimulating factor (CSF-1R) is expressed exclusively in cells of the myeloid lineages as well as trophoblasts. A conserved element in the second intron, Fms-Intronic Regulatory Element (FIRE), is essential for macrophage-specific transcription of the gene. However, the molecular details of how FIRE activity is regulated and how it impacts the Csf1r promoter have not been characterised. Here we show that agents that down-modulate Csf1r mRNA transcription regulated promoter activity altered the occupancy of key FIRE cis-acting elements including RUNX1, AP1, and Sp1 binding sites. We demonstrate that FIRE acts as an anti-sense promoter in macrophages and reversal of FIRE orientation within its native context greatly reduced enhancer activity in macrophages. Mutation of transcription initiation sites within FIRE also reduced transcription. These results demonstrate that FIRE is an orientation-specific transcribed enhancer element. Public Library of Science 2013-01-31 /pmc/articles/PMC3561417/ /pubmed/23383005 http://dx.doi.org/10.1371/journal.pone.0054935 Text en © 2013 Sauter et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Sauter, Kristin A. Bouhlel, M. Amine O’Neal, Julie Sester, David P. Tagoh, Hiromi Ingram, Richard M. Pridans, Clare Bonifer, Constanze Hume, David A. The Function of the Conserved Regulatory Element within the Second Intron of the Mammalian Csf1r Locus |
title | The Function of the Conserved Regulatory Element within the Second Intron of the Mammalian Csf1r Locus |
title_full | The Function of the Conserved Regulatory Element within the Second Intron of the Mammalian Csf1r Locus |
title_fullStr | The Function of the Conserved Regulatory Element within the Second Intron of the Mammalian Csf1r Locus |
title_full_unstemmed | The Function of the Conserved Regulatory Element within the Second Intron of the Mammalian Csf1r Locus |
title_short | The Function of the Conserved Regulatory Element within the Second Intron of the Mammalian Csf1r Locus |
title_sort | function of the conserved regulatory element within the second intron of the mammalian csf1r locus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3561417/ https://www.ncbi.nlm.nih.gov/pubmed/23383005 http://dx.doi.org/10.1371/journal.pone.0054935 |
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