In Search of Novel Targets for Heart Disease: Myocardin and Myocardin-Related Transcriptional Cofactors

Growing evidence suggests that gene-regulatory networks, which are responsible for directing cardiovascular development, are altered under stress conditions in the adult heart. The cardiac gene regulatory network is controlled by cardioenriched transcription factors and multiple-cell-signaling input...

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Main Authors: Alexander T. Mikhailov, Mario Torrado
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Biochemistry Research International
Online Access:http://dx.doi.org/10.1155/2012/973723
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spelling doaj-6266c0a1c6a14050a371bff756142d7d2020-11-24T23:01:59ZengHindawi LimitedBiochemistry Research International2090-22472090-22552012-01-01201210.1155/2012/973723973723In Search of Novel Targets for Heart Disease: Myocardin and Myocardin-Related Transcriptional CofactorsAlexander T. Mikhailov0Mario Torrado1Institute of Health Sciences, University of La Coruña, Campus de Oza, Building El Fortin, Las Jubias Street s/n, La Coruña 15006, SpainInstitute of Health Sciences, University of La Coruña, Campus de Oza, Building El Fortin, Las Jubias Street s/n, La Coruña 15006, SpainGrowing evidence suggests that gene-regulatory networks, which are responsible for directing cardiovascular development, are altered under stress conditions in the adult heart. The cardiac gene regulatory network is controlled by cardioenriched transcription factors and multiple-cell-signaling inputs. Transcriptional coactivators also participate in gene-regulatory circuits as the primary targets of both physiological and pathological signals. Here, we focus on the recently discovered myocardin-(MYOCD) related family of transcriptional cofactors (MRTF-A and MRTF-B) which associate with the serum response transcription factor and activate the expression of a variety of target genes involved in cardiac growth and adaptation to stress via overlapping but distinct mechanisms. We discuss the involvement of MYOCD, MRTF-A, and MRTF-B in the development of cardiac dysfunction and to what extent modulation of the expression of these factors in vivo can correlate with cardiac disease outcomes. A close examination of the findings identifies the MYOCD-related transcriptional cofactors as putative therapeutic targets to improve cardiac function in heart failure conditions through distinct context-dependent mechanisms. Nevertheless, we are in support of further research to better understand the precise role of individual MYOCD-related factors in cardiac function and disease, before any therapeutic intervention is to be entertained in preclinical trials.http://dx.doi.org/10.1155/2012/973723
collection DOAJ
language English
format Article
sources DOAJ
author Alexander T. Mikhailov
Mario Torrado
spellingShingle Alexander T. Mikhailov
Mario Torrado
In Search of Novel Targets for Heart Disease: Myocardin and Myocardin-Related Transcriptional Cofactors
Biochemistry Research International
author_facet Alexander T. Mikhailov
Mario Torrado
author_sort Alexander T. Mikhailov
title In Search of Novel Targets for Heart Disease: Myocardin and Myocardin-Related Transcriptional Cofactors
title_short In Search of Novel Targets for Heart Disease: Myocardin and Myocardin-Related Transcriptional Cofactors
title_full In Search of Novel Targets for Heart Disease: Myocardin and Myocardin-Related Transcriptional Cofactors
title_fullStr In Search of Novel Targets for Heart Disease: Myocardin and Myocardin-Related Transcriptional Cofactors
title_full_unstemmed In Search of Novel Targets for Heart Disease: Myocardin and Myocardin-Related Transcriptional Cofactors
title_sort in search of novel targets for heart disease: myocardin and myocardin-related transcriptional cofactors
publisher Hindawi Limited
series Biochemistry Research International
issn 2090-2247
2090-2255
publishDate 2012-01-01
description Growing evidence suggests that gene-regulatory networks, which are responsible for directing cardiovascular development, are altered under stress conditions in the adult heart. The cardiac gene regulatory network is controlled by cardioenriched transcription factors and multiple-cell-signaling inputs. Transcriptional coactivators also participate in gene-regulatory circuits as the primary targets of both physiological and pathological signals. Here, we focus on the recently discovered myocardin-(MYOCD) related family of transcriptional cofactors (MRTF-A and MRTF-B) which associate with the serum response transcription factor and activate the expression of a variety of target genes involved in cardiac growth and adaptation to stress via overlapping but distinct mechanisms. We discuss the involvement of MYOCD, MRTF-A, and MRTF-B in the development of cardiac dysfunction and to what extent modulation of the expression of these factors in vivo can correlate with cardiac disease outcomes. A close examination of the findings identifies the MYOCD-related transcriptional cofactors as putative therapeutic targets to improve cardiac function in heart failure conditions through distinct context-dependent mechanisms. Nevertheless, we are in support of further research to better understand the precise role of individual MYOCD-related factors in cardiac function and disease, before any therapeutic intervention is to be entertained in preclinical trials.
url http://dx.doi.org/10.1155/2012/973723
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