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The Hippo signal transduction network for exercise physiologists

Journal

JOURNAL OF APPLIED PHYSIOLOGY
Volume 120, Issue 10, Pages 1105-1117

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.01076.2015

Keywords

exercise; Hippo; hypertrophy; skeletal muscle; Yap

Funding

  1. Wenner-Gren Foundation Postdoctoral Fellowship
  2. European Foundation for the Study of Diabetes Albert Renold Travel Fellowship
  3. Novo Nordisk Foundation Challenge Grant
  4. Medical Research Council Grant [99477]
  5. Sarcoma UK
  6. Friends of Anchor
  7. postdoctoral fellowship from the Canadian Institutes of Health Research
  8. MRC [G1100193] Funding Source: UKRI
  9. Medical Research Council [G1100193] Funding Source: researchfish

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The ubiquitous transcriptional coactivators Yap (gene symbol Yap1) and Taz (gene symbol Wwtr1) regulate gene expression mainly by coactivating the Tead transcription factors. Being at the center of the Hippo signaling network, Yap and Taz are regulated by the Hippo kinase cassette and additionally by a plethora of exercise-associated signals and signaling modules. These include mechanotransduction, the AKT-mTORC1 network, the SMAD transcription factors, hypoxia, glucose homeostasis, AMPK, adrenaline/epinephrine and angiotensin II through G protein-coupled receptors, and IL-6. Consequently, exercise should alter Hippo signaling in several organs to mediate at least some aspects of the organ-specific adaptations to exercise. Indeed, Tead1 overexpression in muscle fibers has been shown to promote a fast-to-slow fiber type switch, whereas Yap in muscle fibers and cardiomyocytes promotes skeletal muscle hypertrophy and cardiomyocyte adaptations, respectively. Finally, genome-wide association studies in humans have linked the Hippo pathway members LATS2, TEAD1, YAP1, VGLL2, VGLL3, and VGLL4 to body height, which is a key factor in sports.

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