Literature DB >> 17962623

MCAT elements and the TEF-1 family of transcription factors in muscle development and disease.

Tadashi Yoshida1.   

Abstract

MCAT elements are located in the promoter-enhancer regions of cardiac, smooth, and skeletal muscle-specific genes including cardiac troponin T, beta-myosin heavy chain, smooth muscle alpha-actin, and skeletal alpha-actin, and play a key role in the regulation of these genes during muscle development and disease. The binding factors of MCAT elements are members of the transcriptional enhancer factor-1 (TEF-1) family. However, it has not been fully understood how these transcription factors confer cell-specific expression in muscle, because their expression patterns are relatively broad. Results of recent studies revealed multiple mechanisms whereby TEF-1 family members control MCAT element-dependent muscle-specific gene expression, including posttranslational modifications of TEF-1 family members, the presence of muscle-selective TEF-1 cofactors, and cell-selective control of TEF-1 accessibility to MCAT elements. In addition, of particular interest, recent studies regarding MCAT element-dependent transcription of the myocardin gene and the smooth muscle alpha-actin gene in muscle provide evidence for the transcriptional diversity among distinct cell types and subtypes. This article summarizes the role of MCAT elements and the TEF-1 family of transcription factors in muscle development and disease, and reviews recent progress in our understanding of the transcriptional regulatory mechanisms involved in MCAT element-dependent muscle-specific gene expression.

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Year:  2007        PMID: 17962623     DOI: 10.1161/ATVBAHA.107.155788

Source DB:  PubMed          Journal:  Arterioscler Thromb Vasc Biol        ISSN: 1079-5642            Impact factor:   8.311


  47 in total

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Review 4.  Hippo pathway effectors YAP and TAZ and their association with skeletal muscle ageing.

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7.  Transcription factor TEAD4 regulates expression of myogenin and the unfolded protein response genes during C2C12 cell differentiation.

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Journal:  Cell Death Differ       Date:  2011-06-24       Impact factor: 15.828

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Journal:  Am J Physiol Heart Circ Physiol       Date:  2020-06-05       Impact factor: 4.733

9.  Tead1 is required for maintaining adult cardiomyocyte function, and its loss results in lethal dilated cardiomyopathy.

Authors:  Ruya Liu; Jeongkyung Lee; Byung S Kim; Qiongling Wang; Samuel K Buxton; Nikhil Balasubramanyam; Jean J Kim; Jianrong Dong; Aijun Zhang; Shumin Li; Anisha A Gupte; Dale J Hamilton; James F Martin; George G Rodney; Cristian Coarfa; Xander Ht Wehrens; Vijay K Yechoor; Mousumi Moulik
Journal:  JCI Insight       Date:  2017-09-07

10.  Co-occupancy by multiple cardiac transcription factors identifies transcriptional enhancers active in heart.

Authors:  Aibin He; Sek Won Kong; Qing Ma; William T Pu
Journal:  Proc Natl Acad Sci U S A       Date:  2011-03-17       Impact factor: 11.205

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