Pathological stress induces transcriptional gene reprogramming in the heart muscle, leading to myopathy and heart failure. However, little is known about how the pathological stress triggers the restructuring of chromatin to control myopathic gene expression. This research program focuses on how different chromatin-regulating factors act in concert to establish a repressive chromatin environment to control the expression of alpha-myosin heavy chain (?-MHC), a molecular motor gene whose repression in the stressed hearts contributes to myopathy and heart failure. Four different chromatin regulators-chromatin remodeler, histone methyltransferase, histone deacetylase and DNA methyltransferase-will be examined for their collaborative repression of ?-MHC. Because chemical inhibitors are available to inhibit these chromatin factors, it is possible to develop drus to boost ?- MHC in the failing heart to improve cardiac function. Understanding how these chromatin factors (drug targets) interact will help us design new drugs and understand the synergy/dynamics of potential drugs that inhibit different classes of chromatin regulators.
Aim 1 : Defining specific isoforms of DNA methyltransferase required for ?-MHC repression and heart failure. We will knock out DNA methyltransferase isoforms in the heart muscle of mice and examine the effects on ?-MHC repression in the stressed heart and on the progression of heart failure.
Aim 2 : Determine how chromatin remodeler integrates histone and DNA methyltransferases to silence ?-MHC. We will use animal models, surgical method, and various molecular biology methods (chromatin immunoprecipitation and quantitative PCR) to define the interactions between these chromatin factors crucial for the histone and DNA methylation of ?-MHC.
Aim 3 : Defining how histone deacetylase coordinates with histone and DNA methyltransferases to repress ?-MHC promoter. We will use animal models, surgical methods, and various molecular biology methods (chromatin immunoprecipitation, quantitative PCR, and co-immunoprecipitation) to define the interactions between these chromatin factors that are essential for histone methylation and acetylation, as well as DNA methylation of ?-MHC promoter.
Cardiomyopathy and heart failure is a major cause of morbidity and mortality in our society. Aberrant expression of molecular motor genes in the diseased heart is an essential step toward the development of heart failure. Understanding the mechanisms that control molecular motor gene expression will provide a mechanistic base for designing new treatment for heart failure.
|Yang, Jin; Feng, Xuhui; Zhou, Qiong et al. (2016) Pathological Ace2-to-Ace enzyme switch in the stressed heart is transcriptionally controlled by the endothelial Brg1-FoxM1 complex. Proc Natl Acad Sci U S A 113:E5628-35|
|Han, Pei; Li, Wei; Yang, Jin et al. (2016) Epigenetic response to environmental stress: Assembly of BRG1-G9a/GLP-DNMT3 repressive chromatin complex on Myh6 promoter in pathologically stressed hearts. Biochim Biophys Acta 1863:1772-81|
|Chang, Ching-Pin; Han, Pei (2016) Epigenetic and lncRNA regulation of cardiac pathophysiology. Biochim Biophys Acta 1863:1767-71|
|Han, Pei; Chang, Ching-Pin (2015) Myheart hits the core of chromatin. Cell Cycle 14:787-8|
|Han, Pei; Chang, Ching-Pin (2015) Long non-coding RNA and chromatin remodeling. RNA Biol 12:1094-8|
|Devaux, Yvan; Zangrando, Jennifer; Schroen, Blanche et al. (2015) Long noncoding RNAs in cardiac development and ageing. Nat Rev Cardiol 12:415-25|
|Han, Pei; Li, Wei; Lin, Chiou-Hong et al. (2014) A long noncoding RNA protects the heart from pathological hypertrophy. Nature 514:102-106|
|Van Nostrand, Jeanine L; Brady, Colleen A; Jung, Heiyoun et al. (2014) Inappropriate p53 activation during development induces features of CHARGE syndrome. Nature 514:228-32|
|Yang, Jin; Zeini, Miriam; Lin, Chieh-Yu et al. (2014) Epicardial calcineurin-NFAT signals through Smad2 to direct coronary smooth muscle cell and arterial wall development. Cardiovasc Res 101:120-9|
|Li, Wei; Lin, Chieh-Yu; Shang, Ching et al. (2014) Pbx1 activates Fgf10 in the mesenchyme of developing lungs. Genesis 52:399-407|