Cargando…
Art27 Interacts with GATA4, FOG2 and NKX2.5 and Is a Novel Co-Repressor of Cardiac Genes
Transcription factors play a crucial role in regulation of cardiac biology. FOG-2 is indispensable in this setting, predominantly functioning through a physical interaction with GATA-4. This study aimed to identify novel co-regulators of FOG-2 to further elaborate on its inhibitory activity on GATA-...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990687/ https://www.ncbi.nlm.nih.gov/pubmed/24743694 http://dx.doi.org/10.1371/journal.pone.0095253 |
_version_ | 1782312323597205504 |
---|---|
author | Carter, Daniel R. Buckle, Andrew D. Tanaka, Kumiko Perdomo, Jose Chong, Beng H. |
author_facet | Carter, Daniel R. Buckle, Andrew D. Tanaka, Kumiko Perdomo, Jose Chong, Beng H. |
author_sort | Carter, Daniel R. |
collection | PubMed |
description | Transcription factors play a crucial role in regulation of cardiac biology. FOG-2 is indispensable in this setting, predominantly functioning through a physical interaction with GATA-4. This study aimed to identify novel co-regulators of FOG-2 to further elaborate on its inhibitory activity on GATA-4. The Art27 transcription factor was identified by a yeast-2-hybrid library screen to be a novel FOG-2 protein partner. Characterisation revealed that Art27 is co-expressed with FOG-2 and GATA-4 throughout cardiac myocyte differentiation and in multiple structures of the adult heart. Art27 physically interacts with GATA-4, FOG-2 and other cardiac transcription factors and by this means, down-regulates their activity on cardiac specific promoters α-myosin heavy chain, atrial natriuretic peptide and B-type natriuretic peptide. Regulation of endogenous cardiac genes by Art27 was shown using microarray analysis of P19CL6-Mlc2v-GFP cardiomyocytes. Together these results suggest that Art27 is a novel transcription factor that is involved in downregulation of cardiac specific genes by physically interacting and inhibiting the activity of crucial transcriptions factors involved in cardiac biology. |
format | Online Article Text |
id | pubmed-3990687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39906872014-04-21 Art27 Interacts with GATA4, FOG2 and NKX2.5 and Is a Novel Co-Repressor of Cardiac Genes Carter, Daniel R. Buckle, Andrew D. Tanaka, Kumiko Perdomo, Jose Chong, Beng H. PLoS One Research Article Transcription factors play a crucial role in regulation of cardiac biology. FOG-2 is indispensable in this setting, predominantly functioning through a physical interaction with GATA-4. This study aimed to identify novel co-regulators of FOG-2 to further elaborate on its inhibitory activity on GATA-4. The Art27 transcription factor was identified by a yeast-2-hybrid library screen to be a novel FOG-2 protein partner. Characterisation revealed that Art27 is co-expressed with FOG-2 and GATA-4 throughout cardiac myocyte differentiation and in multiple structures of the adult heart. Art27 physically interacts with GATA-4, FOG-2 and other cardiac transcription factors and by this means, down-regulates their activity on cardiac specific promoters α-myosin heavy chain, atrial natriuretic peptide and B-type natriuretic peptide. Regulation of endogenous cardiac genes by Art27 was shown using microarray analysis of P19CL6-Mlc2v-GFP cardiomyocytes. Together these results suggest that Art27 is a novel transcription factor that is involved in downregulation of cardiac specific genes by physically interacting and inhibiting the activity of crucial transcriptions factors involved in cardiac biology. Public Library of Science 2014-04-17 /pmc/articles/PMC3990687/ /pubmed/24743694 http://dx.doi.org/10.1371/journal.pone.0095253 Text en © 2014 Carter 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 Carter, Daniel R. Buckle, Andrew D. Tanaka, Kumiko Perdomo, Jose Chong, Beng H. Art27 Interacts with GATA4, FOG2 and NKX2.5 and Is a Novel Co-Repressor of Cardiac Genes |
title | Art27 Interacts with GATA4, FOG2 and NKX2.5 and Is a Novel Co-Repressor of Cardiac Genes |
title_full | Art27 Interacts with GATA4, FOG2 and NKX2.5 and Is a Novel Co-Repressor of Cardiac Genes |
title_fullStr | Art27 Interacts with GATA4, FOG2 and NKX2.5 and Is a Novel Co-Repressor of Cardiac Genes |
title_full_unstemmed | Art27 Interacts with GATA4, FOG2 and NKX2.5 and Is a Novel Co-Repressor of Cardiac Genes |
title_short | Art27 Interacts with GATA4, FOG2 and NKX2.5 and Is a Novel Co-Repressor of Cardiac Genes |
title_sort | art27 interacts with gata4, fog2 and nkx2.5 and is a novel co-repressor of cardiac genes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990687/ https://www.ncbi.nlm.nih.gov/pubmed/24743694 http://dx.doi.org/10.1371/journal.pone.0095253 |
work_keys_str_mv | AT carterdanielr art27interactswithgata4fog2andnkx25andisanovelcorepressorofcardiacgenes AT buckleandrewd art27interactswithgata4fog2andnkx25andisanovelcorepressorofcardiacgenes AT tanakakumiko art27interactswithgata4fog2andnkx25andisanovelcorepressorofcardiacgenes AT perdomojose art27interactswithgata4fog2andnkx25andisanovelcorepressorofcardiacgenes AT chongbengh art27interactswithgata4fog2andnkx25andisanovelcorepressorofcardiacgenes |