Glycogenin is dispensable for normal liver glycogen metabolism and body glucose homeostasis

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.

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Publication Details

Journal
International Journal of Biological Macromolecules
Published
2024-12-21
DOI
https://doi.org/10.1016/j.ijbiomac.2024.139084
Citations
6
Primary Topic
Glycogen Storage Diseases and Myoclonus
Type
article
Field-Weighted Citation Impact
2.82

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article

Glycogenin is dispensable for normal liver glycogen metabolism and body glucose homeostasis

Joan J. Guinovart, Robert G. Gilbert, Iliana López‐Soldado, Francisco Vilaplana et al.
6 citations
International Journal of Biological Macromolecules
Glycogen Storage Diseases and Myoclonus
2.82
article

Glycogenin is dispensable for normal liver glycogen metabolism and body glucose homeostasis

Joan J. Guinovart, Robert G. Gilbert, Iliana López‐Soldado, Francisco Vilaplana, Mitchell A. Sullivan, Giorgia Testoni, Xinle Tan, Benjamin L. Schulz, Jordi Durán
article en
6 citations

Abstract

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.

International Journal of Biological MacromoleculesVol. 291
Translational Research Institute (AU), The University of Queensland (AU), University of the Sunshine Coast (AU), Mater Research (AU), Institute for Research in Biomedicine (ES), AlbaNova (SE), Institut Químic de Sarrià (ES), ARC Centre of Excellence for Plant Success in Nature and Agriculture (AU), Yangzhou University (CN), KTH Royal Institute of Technology (SE)
Fundación Ramón Areces, Ministerio de Ciencia, Innovación y Universidades, National Natural Science Foundation of China, Priority Academic Program Development of Jiangsu Higher Education Institutions, European Regional Development Fund, Agencia Estatal de Investigación
Zero hunger
Openalex Percentile: Top 9%
Glycogen Storage Diseases and Myoclonus
2.82
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