Please use this identifier to cite or link to this item: https://doi.org/10.1007/s00418-012-1070-9
Title: Myosin VI in skeletal muscle: Its localization in the sarcoplasmic reticulum, neuromuscular junction and muscle nuclei
Authors: Karolczak, J 
Sobczak, M
Majewski, L
Yeghiazaryan, M
Jakubiec-Puka, A
Ehler, E
Slawinska, U
Wilczyski, G.M
Redowicz, M.J
Keywords: myosin VI
myosin heavy chain
myosin VI
protein binding
animal experiment
animal tissue
article
controlled study
heart muscle
hindlimb
muscle cell
muscle nuclei
neuromuscular synapse
nonhuman
priority journal
protein expression
protein function
protein isolation
protein localization
rat
sarcoplasmic reticulum
skeletal muscle
animal
C57BL mouse
cell nucleus
chemistry
denervation
female
heart muscle cell
metabolism
mouse
neuromuscular synapse
sarcoplasmic reticulum
skeletal muscle
synaptic membrane
Wistar rat
Rattus
Animals
Cell Nucleus
Denervation
Female
Hindlimb
Mice
Mice, Inbred C57BL
Muscle Fibers, Skeletal
Myocytes, Cardiac
Myosin Heavy Chains
Neuromuscular Junction
Protein Binding
Rats
Rats, Wistar
Sarcoplasmic Reticulum
Synaptic Membranes
Issue Date: 2013
Publisher: Springer Verlag
Citation: Karolczak, J, Sobczak, M, Majewski, L, Yeghiazaryan, M, Jakubiec-Puka, A, Ehler, E, Slawinska, U, Wilczyski, G.M, Redowicz, M.J (2013). Myosin VI in skeletal muscle: Its localization in the sarcoplasmic reticulum, neuromuscular junction and muscle nuclei. Histochemistry and Cell Biology 139 (6) : 873-885. ScholarBank@NUS Repository. https://doi.org/10.1007/s00418-012-1070-9
Rights: Attribution 4.0 International
Abstract: Myosin VI (MVI) is a unique unconventional motor moving backwards on actin filaments. In non-muscle cells, it is involved in cell migration, endocytosis and intracellular trafficking, actin cytoskeleton dynamics, and possibly in gene transcription. An important role for MVI in striated muscle functioning was suggested in a report showing that a point mutation (H236R) within the MVI gene was associated with cardiomyopathy (Mohiddin et al., J Med Genet 41:309-314, 2004). Here, we have addressed MVI function in striated muscle by examining its expression and distribution in rat hindlimb skeletal muscle. We found that MVI was present predominantly at the muscle fiber periphery, and it was also localized within muscle nuclei. Analysis of both the hindlimb and cardiac muscle longitudinal sections revealed ~3 ?m striation pattern, corresponding to the sarcoplasmic reticulum. Moreover, MVI was detected in the sarcoplasmic reticulum fractions isolated from skeletal and cardiac muscle. The protein also localized to the postsynaptic region of the neuromuscular junction. In denervated muscle, the defined MVI distribution pattern was abolished and accompanied by significant increase in its amount in the muscle fibers. In addition, we have identified several novel potential MVI-binding partners, which seem to aid our observations that in striated muscle MVI could be involved in postsynaptic trafficking as well as in maintenance of and/or transport within the sarcoplasmic reticulum and non-sarcomeric cytoskeleton. © 2012 The Author(s).
Source Title: Histochemistry and Cell Biology
URI: https://scholarbank.nus.edu.sg/handle/10635/180810
ISSN: 0948-6143
DOI: 10.1007/s00418-012-1070-9
Rights: Attribution 4.0 International
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