Please use this identifier to cite or link to this item: https://doi.org/10.1007/s00418-012-1070-9
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dc.titleMyosin VI in skeletal muscle: Its localization in the sarcoplasmic reticulum, neuromuscular junction and muscle nuclei
dc.contributor.authorKarolczak, J
dc.contributor.authorSobczak, M
dc.contributor.authorMajewski, L
dc.contributor.authorYeghiazaryan, M
dc.contributor.authorJakubiec-Puka, A
dc.contributor.authorEhler, E
dc.contributor.authorSlawinska, U
dc.contributor.authorWilczyski, G.M
dc.contributor.authorRedowicz, M.J
dc.date.accessioned2020-10-27T04:49:31Z
dc.date.available2020-10-27T04:49:31Z
dc.date.issued2013
dc.identifier.citationKarolczak, 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
dc.identifier.issn0948-6143
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/180810
dc.description.abstractMyosin 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).
dc.publisherSpringer Verlag
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectmyosin VI
dc.subjectmyosin heavy chain
dc.subjectmyosin VI
dc.subjectprotein binding
dc.subjectanimal experiment
dc.subjectanimal tissue
dc.subjectarticle
dc.subjectcontrolled study
dc.subjectheart muscle
dc.subjecthindlimb
dc.subjectmuscle cell
dc.subjectmuscle nuclei
dc.subjectneuromuscular synapse
dc.subjectnonhuman
dc.subjectpriority journal
dc.subjectprotein expression
dc.subjectprotein function
dc.subjectprotein isolation
dc.subjectprotein localization
dc.subjectrat
dc.subjectsarcoplasmic reticulum
dc.subjectskeletal muscle
dc.subjectanimal
dc.subjectC57BL mouse
dc.subjectcell nucleus
dc.subjectchemistry
dc.subjectdenervation
dc.subjectfemale
dc.subjectheart muscle cell
dc.subjectmetabolism
dc.subjectmouse
dc.subjectneuromuscular synapse
dc.subjectsarcoplasmic reticulum
dc.subjectskeletal muscle
dc.subjectsynaptic membrane
dc.subjectWistar rat
dc.subjectRattus
dc.subjectAnimals
dc.subjectCell Nucleus
dc.subjectDenervation
dc.subjectFemale
dc.subjectHindlimb
dc.subjectMice
dc.subjectMice, Inbred C57BL
dc.subjectMuscle Fibers, Skeletal
dc.subjectMyocytes, Cardiac
dc.subjectMyosin Heavy Chains
dc.subjectNeuromuscular Junction
dc.subjectProtein Binding
dc.subjectRats
dc.subjectRats, Wistar
dc.subjectSarcoplasmic Reticulum
dc.subjectSynaptic Membranes
dc.typeArticle
dc.contributor.departmentBIOMEDICAL ENGINEERING
dc.description.doi10.1007/s00418-012-1070-9
dc.description.sourcetitleHistochemistry and Cell Biology
dc.description.volume139
dc.description.issue6
dc.description.page873-885
dc.published.statePublished
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