Please use this identifier to cite or link to this item: https://doi.org/10.1038/ncomms9054
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dc.titleTbx15 controls skeletal muscle fibre-type determination and muscle metabolism
dc.contributor.authorLee, K.Y
dc.contributor.authorSingh, M.K
dc.contributor.authorUssar, S
dc.contributor.authorWetzel, P
dc.contributor.authorHirshman, M.F
dc.contributor.authorGoodyear, L.J
dc.contributor.authorKispert, A
dc.contributor.authorKahn, C.R
dc.date.accessioned2020-10-26T09:00:34Z
dc.date.available2020-10-26T09:00:34Z
dc.date.issued2015
dc.identifier.citationLee, K.Y, Singh, M.K, Ussar, S, Wetzel, P, Hirshman, M.F, Goodyear, L.J, Kispert, A, Kahn, C.R (2015). Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism. Nature Communications 6 : 8054. ScholarBank@NUS Repository. https://doi.org/10.1038/ncomms9054
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/180444
dc.description.abstractSkeletal muscle is composed of both slow-twitch oxidative myofibers and fast-twitch glycolytic myofibers that differentially impact muscle metabolism, function and eventually whole-body physiology. Here we show that the mesodermal transcription factor T-box 15 (Tbx15) is highly and specifically expressed in glycolytic myofibers. Ablation of Tbx15 in vivo leads to a decrease in muscle size due to a decrease in the number of glycolytic fibres, associated with a small increase in the number of oxidative fibres. This shift in fibre composition results in muscles with slower myofiber contraction and relaxation, and also decreases whole-body oxygen consumption, reduces spontaneous activity, increases adiposity and glucose intolerance. Mechanistically, ablation of Tbx15 leads to activation of AMPK signalling and a decrease in Igf2 expression. Thus, Tbx15 is one of a limited number of transcription factors to be identified with a critical role in regulating glycolytic fibre identity and muscle metabolism.
dc.publisherNature Publishing Group
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectadenylate kinase
dc.subjectsomatomedin B
dc.subjectTbx15 protein
dc.subjecttranscription factor
dc.subjectunclassified drug
dc.subjectfat intake
dc.subjecthydroxymethylglutaryl coenzyme A reductase kinase
dc.subjectIGF2 protein, mouse
dc.subjectsomatomedin B
dc.subjectT box transcription factor
dc.subjectTBX15 protein, mouse
dc.subjectbiochemistry
dc.subjectbioenergetics
dc.subjectgene expression
dc.subjectglucose
dc.subjectmetabolism
dc.subjectmuscle
dc.subjectoxygen
dc.subjectphysiology
dc.subjectskeletal remains
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectcontrolled study
dc.subjectglucose intolerance
dc.subjectglycolysis
dc.subjectmouse
dc.subjectmuscle contraction
dc.subjectmuscle metabolism
dc.subjectmuscle relaxation
dc.subjectnonhuman
dc.subjectobesity
dc.subjectoxygen consumption
dc.subjectprotein expression
dc.subjectskeletal muscle
dc.subjectadministration and dosage
dc.subjectadverse effects
dc.subjectanimal
dc.subjectcell line
dc.subjectchemically induced
dc.subjectclassification
dc.subjectfat intake
dc.subjectgene expression regulation
dc.subjectgenetics
dc.subjectknockout mouse
dc.subjectmale
dc.subjectmetabolism
dc.subjectoxidation reduction reaction
dc.subjectphysiology
dc.subjectskeletal muscle cell
dc.subjectAMP-Activated Protein Kinases
dc.subjectAnimals
dc.subjectCell Line
dc.subjectDietary Fats
dc.subjectGene Expression Regulation
dc.subjectGlucose Intolerance
dc.subjectInsulin-Like Growth Factor II
dc.subjectMale
dc.subjectMice
dc.subjectMice, Knockout
dc.subjectMuscle Contraction
dc.subjectMuscle Fibers, Skeletal
dc.subjectObesity
dc.subjectOxidation-Reduction
dc.subjectT-Box Domain Proteins
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1038/ncomms9054
dc.description.sourcetitleNature Communications
dc.description.volume6
dc.description.page8054
dc.published.statepublished
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