Transcriptional cofactor Vgll2 is required for functional adaptations of skeletal muscle induced by chronic overload

Masahiko Honda, Hirotsugu Tsuchimochi, Keisuke Hitachi, Seiko Ohno

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Skeletal muscle is composed of heterogeneous populations of myofibers classified as slow- and fast-twitch fibers. Myofiber size and composition are drastically changed in response to physiological demands. We previously showed that transcriptional cofactor vestigial-like (Vgll) 2 is a pivotal regulator of slow muscle gene programming under sedentary conditions. However, whether Vgll2 is required for skeletal muscle adaptations after chronic overload is unclear. Therefore, we investigated the role of Vgll2 in chronic overload-inducing skeletal muscle adaptations using synergist ablation (SA) on plantaris. We found that Vgll2 is an essential regulator of the switch towards a slow-contractile phenotype and oxidative metabolism during chronic overload. Mice lacking Vgll2 exhibited limited fiber type transition and downregulation of genes related to lactate metabolism and their regulator peroxisome proliferator-activated receptor gamma coactivator 1α1, after SA, was augmented in Vgll2-deficient mice compared with in wild-type mice. Mechanistically, increased muscle usage elevated Vgll2 levels and promoted the interaction between Vgll2 and its transcription partners such as TEA domain1 (TEAD1), MEF2c, and NFATc1. Calcium ionophore treatment promoted nuclear translocation of Vgll2 and increased TEAD-dependent MYH7 promotor activity in a Vgll2-dependent manner. Taken together, these data demonstrate that Vgll2 plays an important role for functional adaptation of skeletal muscle to chronic overload.

Original languageEnglish
Pages (from-to)15809-15824
Number of pages16
JournalJournal of Cellular Physiology
Volume234
Issue number9
DOIs
Publication statusPublished - 01-09-2019

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Muscle
Skeletal Muscle
Ablation
Metabolism
Muscles
Calcium Ionophores
PPAR gamma
Genes
Lactic Acid
Down-Regulation
Fibers
Transcription
Phenotype
Switches
Population
Chemical analysis

All Science Journal Classification (ASJC) codes

  • Physiology
  • Clinical Biochemistry
  • Cell Biology

Cite this

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title = "Transcriptional cofactor Vgll2 is required for functional adaptations of skeletal muscle induced by chronic overload",
abstract = "Skeletal muscle is composed of heterogeneous populations of myofibers classified as slow- and fast-twitch fibers. Myofiber size and composition are drastically changed in response to physiological demands. We previously showed that transcriptional cofactor vestigial-like (Vgll) 2 is a pivotal regulator of slow muscle gene programming under sedentary conditions. However, whether Vgll2 is required for skeletal muscle adaptations after chronic overload is unclear. Therefore, we investigated the role of Vgll2 in chronic overload-inducing skeletal muscle adaptations using synergist ablation (SA) on plantaris. We found that Vgll2 is an essential regulator of the switch towards a slow-contractile phenotype and oxidative metabolism during chronic overload. Mice lacking Vgll2 exhibited limited fiber type transition and downregulation of genes related to lactate metabolism and their regulator peroxisome proliferator-activated receptor gamma coactivator 1α1, after SA, was augmented in Vgll2-deficient mice compared with in wild-type mice. Mechanistically, increased muscle usage elevated Vgll2 levels and promoted the interaction between Vgll2 and its transcription partners such as TEA domain1 (TEAD1), MEF2c, and NFATc1. Calcium ionophore treatment promoted nuclear translocation of Vgll2 and increased TEAD-dependent MYH7 promotor activity in a Vgll2-dependent manner. Taken together, these data demonstrate that Vgll2 plays an important role for functional adaptation of skeletal muscle to chronic overload.",
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Transcriptional cofactor Vgll2 is required for functional adaptations of skeletal muscle induced by chronic overload. / Honda, Masahiko; Tsuchimochi, Hirotsugu; Hitachi, Keisuke; Ohno, Seiko.

In: Journal of Cellular Physiology, Vol. 234, No. 9, 01.09.2019, p. 15809-15824.

Research output: Contribution to journalArticle

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