TY - JOUR
T1 - Glycogenin is dispensable for normal liver glycogen metabolism and body glucose homeostasis
AU - Tan, Xinle
AU - Testoni, Giorgia
AU - Sullivan, Mitchell A.
AU - López-Soldado, Iliana
AU - Vilaplana, Francisco
AU - Gilbert, Robert G.
AU - Guinovart, Joan J.
AU - Schulz, Benjamin L.
AU - Duran, Jordi
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2025/2
Y1 - 2025/2
N2 - Glycogen is a glucose-storage polysaccharide molecule present in animals, fungi and bacteria. The enzyme glycogenin can self-glycosylate, forming an oligosaccharide chain that primes glycogen synthesis. This priming role of glycogenin was first believed to be essential for glycogen synthesis, but glycogen was then found in the skeletal muscle, heart, liver and brain of glycogenin-knockout mice (Gyg KO), thereby showing that glycogen can be synthesized without glycogenin. Within the liver, glycogen is present in the form of individual glycogen particles, called β particles, and larger composite aggregates of linked β particles, called α particles. Previous studies suggested that liver glycogenin plays a role in linking β particles into α particles and thus participating in glucose homeostasis, which implies that α particles would be absent in Gyg KO mice liver. Here we test this through targeted characterization of glycogen structure and through proteomic and metabolic studies on Gyg KO mice. The results show that, contrary to what had been believed, glycogenin is not necessary for normal liver-glycogen metabolism.
AB - Glycogen is a glucose-storage polysaccharide molecule present in animals, fungi and bacteria. The enzyme glycogenin can self-glycosylate, forming an oligosaccharide chain that primes glycogen synthesis. This priming role of glycogenin was first believed to be essential for glycogen synthesis, but glycogen was then found in the skeletal muscle, heart, liver and brain of glycogenin-knockout mice (Gyg KO), thereby showing that glycogen can be synthesized without glycogenin. Within the liver, glycogen is present in the form of individual glycogen particles, called β particles, and larger composite aggregates of linked β particles, called α particles. Previous studies suggested that liver glycogenin plays a role in linking β particles into α particles and thus participating in glucose homeostasis, which implies that α particles would be absent in Gyg KO mice liver. Here we test this through targeted characterization of glycogen structure and through proteomic and metabolic studies on Gyg KO mice. The results show that, contrary to what had been believed, glycogenin is not necessary for normal liver-glycogen metabolism.
KW - Glucose metabolism
KW - Glycogen
KW - Glycogen α particles
KW - Glycogenin
KW - Liver
UR - http://www.scopus.com/inward/record.url?scp=85213235068&partnerID=8YFLogxK
U2 - 10.1016/j.ijbiomac.2024.139084
DO - 10.1016/j.ijbiomac.2024.139084
M3 - Article
AN - SCOPUS:85213235068
SN - 0141-8130
VL - 291
JO - International Journal of Biological Macromolecules
JF - International Journal of Biological Macromolecules
M1 - 139084
ER -