Cardiac Expression of ms1/STARS, a Novel Gene Involved in Cardiac Development and Disease, Is Regulated by GATA4

被引:12
|
作者
Ounzain, Samir [1 ,8 ]
Kobayashi, Satoru [2 ]
Peterson, Richard E. [3 ]
He, Aibin [4 ,5 ,6 ]
Motterle, Anna [7 ]
Samani, Nilesh J. [1 ]
Menick, Donald R. [3 ]
Pu, William T. [4 ,5 ,6 ]
Liang, Qiangrong [2 ]
Chong, Nelson W. [1 ]
机构
[1] Univ Leicester, Glenfield Hosp, Cardiol Grp, Dept Cardiovasc Sci, Leicester, Leics, England
[2] Univ S Dakota, Cardiovasc Hlth Res Ctr, Sanford Res, Sioux Falls, SD USA
[3] Med Univ S Carolina, Dept Med, Div Cardiol, Gazes Cardiac Res Inst, Charleston, SC 29425 USA
[4] Harvard Univ, Sch Med, Dept Genet, Boston, MA USA
[5] Childrens Hosp Boston, Dept Cardiol, Boston, MA USA
[6] Harvard Univ, Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[7] Queen Mary Univ London, Barts & London Sch Med & Dent, William Harvey Res Inst, London, England
[8] Univ Lausanne, Expt Cardiol Unit, Sch Med, Dept Med, Lausanne, Switzerland
关键词
SERUM RESPONSE FACTOR; TRANSCRIPTION FACTOR GATA4; CONTRACTILE FUNCTION; TRANSGENIC MICE; SMOOTH-MUSCLE; IN-VITRO; HEART; HYPERTROPHY; MYOCARDIN; NETWORKS;
D O I
10.1128/MCB.06374-11
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ms1/STARS is a novel muscle-specific actin-binding protein that specifically modulates the myocardin-related transcription factor (MRTF)-serum response factor (SRF) regulatory axis within striated muscle. This ms1/STARS-dependent regulatory axis is of central importance within the cardiac gene regulatory network and has been implicated in cardiac development and postnatal cardiac function/homeostasis. The dysregulation of ms1/STARS is associated with and causative of pathological cardiac phenotypes, including cardiac hypertrophy and cardiomyopathy. In order to gain an understanding of the mechanisms governing ms1/STARS expression in the heart, we have coupled a comparative genomic in silico analysis with reporter, gain-of-function, and loss-of-function approaches. Through this integrated analysis, we have identified three evolutionarily conserved regions (ECRs), alpha, SINA, and DINA, that act as cis-regulatory modules and confer differential cardiac cell-specific activity. Two of these ECRs, alpha and DINA, displayed distinct regulatory sensitivity to the core cardiac transcription factor GATA4. Overall, our results demonstrate that within embryonic, neonatal, and adult hearts, GATA4 represses ms1/STARS expression with the pathologically associated depletion of GATA4 (type 1/type 2 diabetic models), resulting in ms1/STARS upregulation. This GATA4-dependent repression of ms1/STARS expression has major implications for MRTF-SRF signaling in the context of cardiac development and disease.
引用
收藏
页码:1830 / 1843
页数:14
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