Literature DB >> 20847312

Myomasp/LRRC39, a heart- and muscle-specific protein, is a novel component of the sarcomeric M-band and is involved in stretch sensing.

Rainer D Will1, Matthias Eden, Steffen Just, Arne Hansen, Alexandra Eder, Derk Frank, Christian Kuhn, Thalia S Seeger, Ulrike Oehl, Stefan Wiemann, Bernhard Korn, Manfred Koegl, Wolfgang Rottbauer, Thomas Eschenhagen, Hugo A Katus, Norbert Frey.   

Abstract

RATIONALE AND
OBJECTIVE: The M-band represents a transverse structure in the center of the sarcomeric A-band and provides an anchor for the myosin-containing thick filaments. In contrast to other sarcomeric structures, eg, the Z-disc, only few M-band-specific proteins have been identified to date, and its exact molecular composition remains unclear. METHODS AND
RESULTS: Using a bioinformatic approach to identify novel heart- and muscle-specific genes, we found a leucine rich protein, myomasp (Myosin-interacting, M-band-associated stress-responsive protein)/LRRC39. RT-PCR and Northern and Western blot analyses confirmed a cardiac-enriched expression pattern, and immunolocalization of myomasp revealed a strong and specific signal at the sarcomeric M-band. Yeast 2-hybrid screens, as well as coimmunoprecipitation experiments, identified the C terminus of myosin heavy chain (MYH)7 as an interaction partner for myomasp. Knockdown of myomasp in neonatal rat ventricular myocytes (NRVCMs) led to a significant upregulation of the stretch-sensitive genes GDF-15 and BNP. Conversely, the expression of MYH7 and the M-band proteins myomesin-1 and -2 was found to be markedly reduced. Mechanistically, knockdown of myomasp in NRVCM led to a dose-dependent suppression of serum response factor-dependent gene expression, consistent with earlier observations linking the M-band to serum response factor-mediated signaling. Finally, downregulation of myomasp/LRRC39 in spontaneously beating engineered heart tissue constructs resulted in significantly lower force generation and reduced fractional shortening. Likewise, knockdown of the myomasp/LRRC39 ortholog in zebrafish resulted in severely impaired heart function and cardiomyopathy in vivo.
CONCLUSIONS: These findings reveal myomasp as a previously unrecognized component of an M-band-associated signaling pathway that regulates cardiomyocyte gene expression in response to biomechanical stress.

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Year:  2010        PMID: 20847312     DOI: 10.1161/CIRCRESAHA.110.222372

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  24 in total

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6.  LRRC10 is required to maintain cardiac function in response to pressure overload.

Authors:  Matthew J Brody; Li Feng; Adrian C Grimes; Timothy A Hacker; Timothy M Olson; Timothy J Kamp; Ravi C Balijepalli; Youngsook Lee
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8.  Ablation of the cardiac-specific gene leucine-rich repeat containing 10 (Lrrc10) results in dilated cardiomyopathy.

Authors:  Matthew J Brody; Timothy A Hacker; Jitandrakumar R Patel; Li Feng; Junichi Sadoshima; Sergei G Tevosian; Ravi C Balijepalli; Richard L Moss; Youngsook Lee
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9.  EH-myomesin splice isoform is a novel marker for dilated cardiomyopathy.

Authors:  Roman Schoenauer; Maximilian Y Emmert; Allison Felley; Elisabeth Ehler; Chad Brokopp; Benedikt Weber; Mohamed Nemir; Giuseppe G Faggian; Thierry Pedrazzini; Volkmar Falk; Simon P Hoerstrup; Irina Agarkova
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Review 10.  Zebrafish as a model to study cardiac development and human cardiac disease.

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Journal:  Cardiovasc Res       Date:  2011-05-19       Impact factor: 10.787

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