FOXO1 activates glutamine synthetase gene in mouse skeletal muscles through a region downstream of 3’-UTR

Possible contribution to ammonia detoxification

Yasutomi Kamei, Maki Hattori, Yukino Hatazawa, Tomomi Kasahara, Masanobu Kanou, Sayaka Kanai, Xunmei Yuan, Takayoshi Suganami, Wouter H. Lamers, Tadahiro Kitamura, Yoshihiro Ogawa

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Skeletal mus- cle is a reservoir of energy in the form of protein, which is degraded under catabolic conditions, resulting in the formation of amino acids and ammonia as a byproduct. The expression of FOXO1, a forkhead- type transcription factor, increases during starvation and exercise. In agreement, transgenic FOXO1-Tg mice that overexpress FOXO1 in skeletal muscle exhibit muscle atrophy. The aim of this study was to examine the role of FOXO1 in amino acid metabolism. The mRNA and protein expressions of glutamine synthetase (GS) were increased in skeletal muscle of FOXO1-Tg mice. Fasting induced FOXO1 and GS expression in wild-type mice but hardly increased GS expression in muscle-specific FOXO1 knockout (FOXO1-KO) mice. Activation of FOXO1 also increased GS mRNA and protein expression in C2C12 myoblasts. Using a transient transfection reporter assay, we observed that FOXO1 activated the GS reporter construct. Mutation of a putative FOXO1-binding consensus sequence in the downstream genomic region of GS decreased basal and FOXO1-dependent re- porter activity significantly. A chromatin immunoprecipitation assay showed that FOXO1 was recruited to the 3= region of GS in C2C12 myoblasts. These results suggest that FOXO1 directly upregulates GS expression. GS is considered to mediate ammonia clearance in skel- etal muscle. In agreement, an intravenous ammonia challenge in- creased blood ammonia concentrations to a twofold higher level in FOXO1-KO than in wild-type mice, demonstrating that the capacity for ammonia disposal correlated inversely with the expression of GS in muscle. These data indicate that FOXO1 plays a role in amino acid metabolism during protein degradation in skeletal muscle.

Original languageEnglish
Pages (from-to)E485-E493
JournalAmerican Journal of Physiology - Endocrinology and Metabolism
Volume307
Issue number6
DOIs
Publication statusPublished - Sep 15 2014
Externally publishedYes

Fingerprint

Glutamate-Ammonia Ligase
3' Untranslated Regions
Ammonia
Skeletal Muscle
Genes
Myoblasts
Amino Acids
Forkhead Transcription Factors
Muscles
Messenger RNA
Proteins
Muscular Atrophy
Chromatin Immunoprecipitation
Consensus Sequence
Starvation
Knockout Mice
Proteolysis
Transfection
Fasting
Up-Regulation

All Science Journal Classification (ASJC) codes

  • Endocrinology, Diabetes and Metabolism
  • Physiology
  • Physiology (medical)

Cite this

FOXO1 activates glutamine synthetase gene in mouse skeletal muscles through a region downstream of 3’-UTR : Possible contribution to ammonia detoxification. / Kamei, Yasutomi; Hattori, Maki; Hatazawa, Yukino; Kasahara, Tomomi; Kanou, Masanobu; Kanai, Sayaka; Yuan, Xunmei; Suganami, Takayoshi; Lamers, Wouter H.; Kitamura, Tadahiro; Ogawa, Yoshihiro.

In: American Journal of Physiology - Endocrinology and Metabolism, Vol. 307, No. 6, 15.09.2014, p. E485-E493.

Research output: Contribution to journalArticle

Kamei, Yasutomi ; Hattori, Maki ; Hatazawa, Yukino ; Kasahara, Tomomi ; Kanou, Masanobu ; Kanai, Sayaka ; Yuan, Xunmei ; Suganami, Takayoshi ; Lamers, Wouter H. ; Kitamura, Tadahiro ; Ogawa, Yoshihiro. / FOXO1 activates glutamine synthetase gene in mouse skeletal muscles through a region downstream of 3’-UTR : Possible contribution to ammonia detoxification. In: American Journal of Physiology - Endocrinology and Metabolism. 2014 ; Vol. 307, No. 6. pp. E485-E493.
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