Cardiac expression of ms1/STARS, a novel gene involved in cardiac development and disease, is regulated by GATA4.


Autoria(s): Ounzain S.; Kobayashi S.; Peterson R.E.; He A.; Motterle A.; Samani N.J.; Menick D.R.; Pu W.T.; Liang Q.; Chong N.W.
Data(s)

2012

Resumo

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), α, SINA, and DINA, that act as cis-regulatory modules and confer differential cardiac cell-specific activity. Two of these ECRs, α 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.

Identificador

http://serval.unil.ch/?id=serval:BIB_0B25C66D40C3

isbn:1098-5549 (Electronic)

pmid:22431517

doi:10.1128/MCB.06374-11

isiid:000303840100006

Idioma(s)

en

Fonte

Molecular and Cellular Biology, vol. 32, no. 10, pp. 1830-1843

Tipo

info:eu-repo/semantics/article

article