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Axin-mediated regulation of lifespan and muscle health in C. elegans involves AMPK-FOXO signaling
by
Gupta, Bhagwati P
, Mallick, Avijit
in
Aging
/ Cell Biology
/ Forkhead protein
/ Gene expression
/ Insulin
/ Insulin-like growth factor I
/ Kinases
/ Life span
/ Mitochondria
/ Muscles
/ Phosphorylation
/ Risk factors
2020
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Axin-mediated regulation of lifespan and muscle health in C. elegans involves AMPK-FOXO signaling
by
Gupta, Bhagwati P
, Mallick, Avijit
in
Aging
/ Cell Biology
/ Forkhead protein
/ Gene expression
/ Insulin
/ Insulin-like growth factor I
/ Kinases
/ Life span
/ Mitochondria
/ Muscles
/ Phosphorylation
/ Risk factors
2020
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Do you wish to request the book?
Axin-mediated regulation of lifespan and muscle health in C. elegans involves AMPK-FOXO signaling
by
Gupta, Bhagwati P
, Mallick, Avijit
in
Aging
/ Cell Biology
/ Forkhead protein
/ Gene expression
/ Insulin
/ Insulin-like growth factor I
/ Kinases
/ Life span
/ Mitochondria
/ Muscles
/ Phosphorylation
/ Risk factors
2020
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Axin-mediated regulation of lifespan and muscle health in C. elegans involves AMPK-FOXO signaling
Paper
Axin-mediated regulation of lifespan and muscle health in C. elegans involves AMPK-FOXO signaling
2020
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Overview
Aging is a significant risk factor for several diseases. Studies have uncovered multiple signaling pathways that modulate the process of aging including the Insulin/IGF-1 signaling (IIS). In C. elegans the key regulator of IIS is DAF-16/FOXO whose activity is regulated by phosphorylation. A major kinase involved in DAF-16-mediated lifespan extension is the AMPK catalytic subunit homolog, AAK-2. In this study, we demonstrate a novel role of PRY-1/Axin in AAK-2 activation to regulate DAF-16 function. The pry-1 transcriptome contains many genes associated with aging and muscle function. Consistent with this, pry-1 is strongly expressed in muscles and muscle-specific overexpression of pry-1 extends the lifespan, delays muscle aging, and improves mitochondrial morphology in DAF-16-dependent manner. Furthermore, PRY-1 is necessary for AAK-2 phosphorylation. Together, our data demonstrate a crucial role of PRY-1 in maintaining the lifespan and muscle health. Since muscle health declines with age, our study offers new possibilities to manipulate Axin function to delay muscle aging and improve lifespan. Competing Interest Statement The authors have declared no competing interest.
Publisher
Cold Spring Harbor Laboratory Press,Cold Spring Harbor Laboratory
Subject
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