Sarcomeres regulate cardiomyocyte maturation through MRTF-SRF signaling
guo, Y.; Jardin, B.; Sethi, I.; Ma, Q.; Moghadaszadeh, B.; Troiano, E.; Trembley, M.; Small, E.; Yuan, G.-C.; Beggs, A.; Pu, W.
Show abstract
Cardiomyocyte maturation is essential for robust heart contraction throughout life. The signaling networks governing cardiomyocyte maturation remain poorly defined. Our prior studies established the transcription factor SRF as a key regulator of the assembly of sarcomeres, the contractile unit of cardiomyocytes. Whether sarcomeres regulate other aspects of maturation remains unclear. Here we generated mice with cardiomyocyte specific, mosaic mutation of -actinin-2 (Actn2), a key organizer of sarcomeres, to study its cell-autonomous role in cardiomyocyte maturation. In addition to the expected structural defects, Actn2 mutation triggered dramatic transcriptional dysregulation, which strongly correlated with transcriptional changes observed in SRF-depleted cardiomyocytes. Actn2 mutation increased monomeric actin, which perturbed the nuclear localization of the SRF cofactor MRTFA. Overexpression of a dominant-negative MRTFA mutant was sufficient to recapitulate the transcriptional and morphological defects in Actn2 and Srf mutant cardiomyocytes. Together, we demonstrate that ACTN2-based sarcomere assembly and MRTF-SRF signaling establish a positive feedback loop that promotes cardiomyocyte maturation.
Matching journals
The top 7 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Coordinated Tbx3/Tbx5 transcriptional control of the adult ventricular conduction system 96%
- In vivo proximity labeling identifies cardiomyocyte protein networks during zebrafish heart regeneration 96%
- The EMT transcription factor Snai1 maintains myocardial wall integrity by repressing intermediate filament gene expression 96%
Similar papers in this journal
- A Conserved Mechanism of Cardiac Hypertrophy Regression through FoxO1 93%
- Molecular mechanisms controlling the biogenesis of the TGF-β signal Vg1 92%
- Dilated cardiomyopathy-associated skeletal muscle actin (ACTA1) mutation R256H disrupts actin structure and function and causes cardiomyocyte hypocontractility 92%
Similar papers in this journal
- Tbx5 maintains atrial identity by regulating an atrial enhancer network 95%
- Ablation of three major phospho-sites in RyR2 preserves the global adrenergic response but creates an arrhythmogenic substrate 94%
- A disrupted compartment boundary underlies abnormal cardiac patterning and congenital heart defects 94%
Similar papers in this journal
- A microRNA program controls the transition of cardiomyocyte hyperplasia to hypertrophy and stimulates mammalian cardiac regeneration 96%
- Mitochondrial CaMKII causes metabolic reprogramming, energetic insufficiency, and dilated cardiomyopathy 95%
- Mitochondrial fission process 1 (MTFP1) controls bioenergetic efficiency and prevents inflammatory cardiomyopathy and heart failure in mice 95%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.