Please use this identifier to cite or link to this item: https://doi.org/10.1038/ncomms9054
Title: Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism
Authors: Lee, K.Y
Singh, M.K 
Ussar, S
Wetzel, P
Hirshman, M.F
Goodyear, L.J
Kispert, A
Kahn, C.R
Keywords: adenylate kinase
somatomedin B
Tbx15 protein
transcription factor
unclassified drug
fat intake
hydroxymethylglutaryl coenzyme A reductase kinase
IGF2 protein, mouse
somatomedin B
T box transcription factor
TBX15 protein, mouse
biochemistry
bioenergetics
gene expression
glucose
metabolism
muscle
oxygen
physiology
skeletal remains
animal cell
animal experiment
animal tissue
Article
controlled study
glucose intolerance
glycolysis
mouse
muscle contraction
muscle metabolism
muscle relaxation
nonhuman
obesity
oxygen consumption
protein expression
skeletal muscle
administration and dosage
adverse effects
animal
cell line
chemically induced
classification
fat intake
gene expression regulation
genetics
knockout mouse
male
metabolism
oxidation reduction reaction
physiology
skeletal muscle cell
AMP-Activated Protein Kinases
Animals
Cell Line
Dietary Fats
Gene Expression Regulation
Glucose Intolerance
Insulin-Like Growth Factor II
Male
Mice
Mice, Knockout
Muscle Contraction
Muscle Fibers, Skeletal
Obesity
Oxidation-Reduction
T-Box Domain Proteins
Issue Date: 2015
Publisher: Nature Publishing Group
Citation: Lee, 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
Rights: Attribution 4.0 International
Abstract: Skeletal 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.
Source Title: Nature Communications
URI: https://scholarbank.nus.edu.sg/handle/10635/180444
ISSN: 2041-1723
DOI: 10.1038/ncomms9054
Rights: Attribution 4.0 International
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