1. MURC, a muscle-restricted coiled-coil protein that modulates the Rho/ROCK pathway, induces cardiac dysfunction and conduction disturbance.
- Author
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Ogata T, Ueyama T, Isodono K, Tagawa M, Takehara N, Kawashima T, Harada K, Takahashi T, Shioi T, Matsubara H, and Oh H
- Subjects
- Amino Acid Sequence, Animals, Base Sequence, Carrier Proteins genetics, Carrier Proteins metabolism, Cells, Cultured, Cloning, Molecular, DNA Primers genetics, Heart Diseases genetics, Heart Diseases physiopathology, Humans, Mice, Mice, Transgenic, Molecular Sequence Data, Muscle Proteins chemistry, Muscle Proteins genetics, Myocytes, Cardiac metabolism, Phosphate-Binding Proteins, RNA, Messenger genetics, RNA, Messenger metabolism, Rats, Recombinant Proteins chemistry, Recombinant Proteins genetics, Recombinant Proteins metabolism, Sequence Homology, Amino Acid, Signal Transduction, Two-Hybrid System Techniques, rhoA GTP-Binding Protein metabolism, Heart Conduction System physiopathology, Heart Diseases etiology, Muscle Proteins metabolism, rho GTP-Binding Proteins metabolism, rho-Associated Kinases metabolism
- Abstract
We identified a novel muscle-restricted putative coiled-coil protein, MURC, which is evolutionarily conserved from frog to human. MURC was localized to the cytoplasm with accumulation in the Z-line of the sarcomere in the murine adult heart. MURC mRNA expression in the heart increased during the developmental process from the embryonic stage to adulthood. In response to pressure overload, MURC mRNA expression increased in the hypertrophied heart. Using the yeast two-hybrid system, we identified the serum deprivation response (SDPR) protein, a phosphatidylserine-binding protein, as a MURC-binding protein. MURC induced activation of the RhoA/ROCK pathway, which modulated serum response factor-mediated atrial natriuretic peptide (ANP) expression and myofibrillar organization. SDPR augmented MURC-induced transactivation of the ANP promoter in cardiomyocytes, and RNA interference of SDPR attenuated the action of MURC on the ANP promoter. Transgenic mice expressing cardiac-specific MURC (Tg-MURC) exhibited cardiac contractile dysfunction and atrioventricular (AV) conduction disturbances with atrial chamber enlargement, reduced thickness of the ventricular wall, and interstitial fibrosis. Spontaneous episodes of atrial fibrillation and AV block were observed in Tg-MURC mice. These findings indicate that MURC modulates RhoA signaling and that MURC plays an important role in the development of cardiac dysfunction and conduction disturbance with increased vulnerability to atrial arrhythmias.
- Published
- 2008
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