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EGR1 Functions as a Potent Repressor of MEF2 Transcriptional Activity
by
Feng, Yi
, Cooper, Olivia
, Naya, Francisco J.
, Kontor, Akuah
, Desjardins, Cody A.
, Nocco, Sarah E.
in
Animals
/ Binding sites
/ Bioinformatics
/ Cardiomyocytes
/ Cell culture
/ Cloning
/ Computational Biology
/ Cytoskeleton
/ Deoxyribonucleic acid
/ DNA
/ Early Growth Response Protein 1 - genetics
/ Early Growth Response Protein 1 - metabolism
/ EGR-1 protein
/ Gene expression
/ Gene regulation
/ Genes
/ Heart
/ HEK293 Cells
/ Homeostasis
/ Humans
/ Kinases
/ MEF2 Transcription Factors - genetics
/ MEF2 Transcription Factors - metabolism
/ Molecular biology
/ Muscle contraction
/ Muscles
/ Myocyte enhancer factor 2
/ Myocyte-specific enhancer-binding factor 2
/ Myocytes, Cardiac - metabolism
/ Penicillin
/ Physiological aspects
/ Promoter Regions, Genetic
/ Protein Binding
/ Proteins
/ Rats
/ Rodents
/ Transcription (Genetics)
/ Transcription factors
/ Transcription, Genetic - genetics
/ Transcriptional Activation
2015
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EGR1 Functions as a Potent Repressor of MEF2 Transcriptional Activity
by
Feng, Yi
, Cooper, Olivia
, Naya, Francisco J.
, Kontor, Akuah
, Desjardins, Cody A.
, Nocco, Sarah E.
in
Animals
/ Binding sites
/ Bioinformatics
/ Cardiomyocytes
/ Cell culture
/ Cloning
/ Computational Biology
/ Cytoskeleton
/ Deoxyribonucleic acid
/ DNA
/ Early Growth Response Protein 1 - genetics
/ Early Growth Response Protein 1 - metabolism
/ EGR-1 protein
/ Gene expression
/ Gene regulation
/ Genes
/ Heart
/ HEK293 Cells
/ Homeostasis
/ Humans
/ Kinases
/ MEF2 Transcription Factors - genetics
/ MEF2 Transcription Factors - metabolism
/ Molecular biology
/ Muscle contraction
/ Muscles
/ Myocyte enhancer factor 2
/ Myocyte-specific enhancer-binding factor 2
/ Myocytes, Cardiac - metabolism
/ Penicillin
/ Physiological aspects
/ Promoter Regions, Genetic
/ Protein Binding
/ Proteins
/ Rats
/ Rodents
/ Transcription (Genetics)
/ Transcription factors
/ Transcription, Genetic - genetics
/ Transcriptional Activation
2015
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EGR1 Functions as a Potent Repressor of MEF2 Transcriptional Activity
by
Feng, Yi
, Cooper, Olivia
, Naya, Francisco J.
, Kontor, Akuah
, Desjardins, Cody A.
, Nocco, Sarah E.
in
Animals
/ Binding sites
/ Bioinformatics
/ Cardiomyocytes
/ Cell culture
/ Cloning
/ Computational Biology
/ Cytoskeleton
/ Deoxyribonucleic acid
/ DNA
/ Early Growth Response Protein 1 - genetics
/ Early Growth Response Protein 1 - metabolism
/ EGR-1 protein
/ Gene expression
/ Gene regulation
/ Genes
/ Heart
/ HEK293 Cells
/ Homeostasis
/ Humans
/ Kinases
/ MEF2 Transcription Factors - genetics
/ MEF2 Transcription Factors - metabolism
/ Molecular biology
/ Muscle contraction
/ Muscles
/ Myocyte enhancer factor 2
/ Myocyte-specific enhancer-binding factor 2
/ Myocytes, Cardiac - metabolism
/ Penicillin
/ Physiological aspects
/ Promoter Regions, Genetic
/ Protein Binding
/ Proteins
/ Rats
/ Rodents
/ Transcription (Genetics)
/ Transcription factors
/ Transcription, Genetic - genetics
/ Transcriptional Activation
2015
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EGR1 Functions as a Potent Repressor of MEF2 Transcriptional Activity
Journal Article
EGR1 Functions as a Potent Repressor of MEF2 Transcriptional Activity
2015
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Overview
The myocyte enhancer factor 2 (MEF2) transcription factor requires interactions with co-factors for precise regulation of its target genes. Our lab previously reported that the mammalian MEF2A isoform regulates the cardiomyocyte costamere, a critical muscle-specific focal adhesion complex involved in contractility, through its transcriptional control of genes encoding proteins localized to this cytoskeletal structure. To further dissect the transcriptional mechanisms of costamere gene regulation and identify potential co-regulators of MEF2A, a bioinformatics analysis of transcription factor binding sites was performed using the proximal promoter regions of selected costamere genes. One of these predicted sites belongs to the early growth response (EGR) transcription factor family. The EGR1 isoform has been shown to be involved in a number of pathways in cardiovascular homeostasis and disease, making it an intriguing candidate MEF2 coregulator to further characterize. Here, we demonstrate that EGR1 interacts with MEF2A and is a potent and specific repressor of MEF2 transcriptional activity. Furthermore, we show that costamere gene expression in cardiomyocytes is dependent on EGR1 transcriptional activity. This study identifies a mechanism by which MEF2 activity can be modulated to ensure that costamere gene expression is maintained at levels commensurate with cardiomyocyte contractile activity.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Cloning
/ DNA
/ Early Growth Response Protein 1 - genetics
/ Early Growth Response Protein 1 - metabolism
/ Genes
/ Heart
/ Humans
/ Kinases
/ MEF2 Transcription Factors - genetics
/ MEF2 Transcription Factors - metabolism
/ Muscles
/ Myocyte-specific enhancer-binding factor 2
/ Myocytes, Cardiac - metabolism
/ Proteins
/ Rats
/ Rodents
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