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Cell-specific expression of ENACα gene by FOXA1 in the glucocorticoid receptor pathway
INTRODUCTION: The glucocorticoid receptor (GR) is one of the most widely studied ligand-dependent nuclear receptors. The combination of transcriptional regulatory factors required for the expression of individual genes targeted by GR varies across cell types; however, the mechanisms underlying this...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450284/ https://www.ncbi.nlm.nih.gov/pubmed/32838581 http://dx.doi.org/10.1177/2058738420946192 |
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author | Chung, Young Sun Jin, Hong Lan Jeong, Kwang Won |
author_facet | Chung, Young Sun Jin, Hong Lan Jeong, Kwang Won |
author_sort | Chung, Young Sun |
collection | PubMed |
description | INTRODUCTION: The glucocorticoid receptor (GR) is one of the most widely studied ligand-dependent nuclear receptors. The combination of transcriptional regulatory factors required for the expression of individual genes targeted by GR varies across cell types; however, the mechanisms underlying this cell type–specific regulation of gene expression are not yet clear. METHODS: Here, we investigated genes regulated by GR in two different cell lines, A549 and ARPE-19, and examined how gene expression varied according to the effect of pioneer factors using RNA-seq and RT-qPCR. RESULTS: Our RNA-seq results identified 19 and 63 genes regulated by GR that are ARPE-19-specific and A549-specific, respectively, suggesting that GR induces the expression of different sets of genes in a cell type–specific manner. RT-qPCR confirmed that the epithelial sodium channel (ENACα) gene is an ARPE-19 cell-specific GR target gene, whereas the FK506 binding protein 5 (FKBP5) gene was A549 cell-specific. There was a significant decrease in ENACα expression in FOXA1-deficient ARPE-19 cells, suggesting that FOXA1 might function as a pioneer factor enabling the selective expression of ENACα in ARPE-19 cells but not in A549 cells. CONCLUSION: These findings indicate that ENACα expression in ARPE-19 cells is regulated by FOXA1 and provide insights into the molecular mechanisms of cell type–specific expression of GR-regulated genes. |
format | Online Article Text |
id | pubmed-7450284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-74502842020-09-11 Cell-specific expression of ENACα gene by FOXA1 in the glucocorticoid receptor pathway Chung, Young Sun Jin, Hong Lan Jeong, Kwang Won Int J Immunopathol Pharmacol Original Research Article INTRODUCTION: The glucocorticoid receptor (GR) is one of the most widely studied ligand-dependent nuclear receptors. The combination of transcriptional regulatory factors required for the expression of individual genes targeted by GR varies across cell types; however, the mechanisms underlying this cell type–specific regulation of gene expression are not yet clear. METHODS: Here, we investigated genes regulated by GR in two different cell lines, A549 and ARPE-19, and examined how gene expression varied according to the effect of pioneer factors using RNA-seq and RT-qPCR. RESULTS: Our RNA-seq results identified 19 and 63 genes regulated by GR that are ARPE-19-specific and A549-specific, respectively, suggesting that GR induces the expression of different sets of genes in a cell type–specific manner. RT-qPCR confirmed that the epithelial sodium channel (ENACα) gene is an ARPE-19 cell-specific GR target gene, whereas the FK506 binding protein 5 (FKBP5) gene was A549 cell-specific. There was a significant decrease in ENACα expression in FOXA1-deficient ARPE-19 cells, suggesting that FOXA1 might function as a pioneer factor enabling the selective expression of ENACα in ARPE-19 cells but not in A549 cells. CONCLUSION: These findings indicate that ENACα expression in ARPE-19 cells is regulated by FOXA1 and provide insights into the molecular mechanisms of cell type–specific expression of GR-regulated genes. SAGE Publications 2020-08-24 /pmc/articles/PMC7450284/ /pubmed/32838581 http://dx.doi.org/10.1177/2058738420946192 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Article Chung, Young Sun Jin, Hong Lan Jeong, Kwang Won Cell-specific expression of ENACα gene by FOXA1 in the glucocorticoid receptor pathway |
title | Cell-specific expression of ENACα gene by FOXA1 in
the glucocorticoid receptor pathway |
title_full | Cell-specific expression of ENACα gene by FOXA1 in
the glucocorticoid receptor pathway |
title_fullStr | Cell-specific expression of ENACα gene by FOXA1 in
the glucocorticoid receptor pathway |
title_full_unstemmed | Cell-specific expression of ENACα gene by FOXA1 in
the glucocorticoid receptor pathway |
title_short | Cell-specific expression of ENACα gene by FOXA1 in
the glucocorticoid receptor pathway |
title_sort | cell-specific expression of enacα gene by foxa1 in
the glucocorticoid receptor pathway |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450284/ https://www.ncbi.nlm.nih.gov/pubmed/32838581 http://dx.doi.org/10.1177/2058738420946192 |
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