Ryanodine receptors are part of the myospryn complex in cardiac muscle

Autor: Benson, Matthew A., Tinsley, Caroline L., Waite, Adrian J., Carlisle, Francesca A., Sweet, Steve M. M., Ehler, Elisabeth, George, Christopher H., Lai, F. Anthony, Martin-Rendon, Enca, Blake, Derek J.
Jazyk: angličtina
Rok vydání: 2017
Předmět:
Zdroj: Benson, M A, Tinsley, C L, Waite, A J, Carlisle, F A, Sweet, S M M, Ehler, E, George, C H, Lai, F A, Martin-Rendon, E & Blake, D J 2017, ' Ryanodine receptors are part of the myospryn complex in cardiac muscle ', Scientific Reports, vol. 7, no. 1, 6312 . https://doi.org/10.1038/s41598-017-06395-6
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Scientific Reports
ISSN: 2045-2322
DOI: 10.1038/s41598-017-06395-6
Popis: The Cardiomyopathy–associated gene 5 (Cmya5) encodes myospryn, a large tripartite motif (TRIM)-related protein found predominantly in cardiac and skeletal muscle. Cmya5 is an expression biomarker for a number of diseases affecting striated muscle and may also be a schizophrenia risk gene. To further understand the function of myospryn in striated muscle, we searched for additional myospryn paralogs. Here we identify a novel muscle-expressed TRIM-related protein minispryn, encoded by Fsd2, that has extensive sequence similarity with the C-terminus of myospryn. Cmya5 and Fsd2 appear to have originated by a chromosomal duplication and are found within evolutionarily-conserved gene clusters on different chromosomes. Using immunoaffinity purification and mass spectrometry we show that minispryn co-purifies with myospryn and the major cardiac ryanodine receptor (RyR2) from heart. Accordingly, myospryn, minispryn and RyR2 co-localise at the junctional sarcoplasmic reticulum of isolated cardiomyocytes. Myospryn redistributes RyR2 into clusters when co-expressed in heterologous cells whereas minispryn lacks this activity. Together these data suggest a novel role for the myospryn complex in the assembly of ryanodine receptor clusters in striated muscle.
Databáze: OpenAIRE