PUBLICATION

Disorder of glucose metabolism and impairing energy metabolism by pfkma and pfkmb knockout zebrafish

Authors
Liu, N., Li, M., Liu, T., Wang, J., Zhang, B., Zhang, M.
ID
ZDB-PUB-250728-4
Date
2025
Source
General and comparative endocrinology : 114787 (Journal)
Registered Authors
Zhang, Bo
Keywords
Diabetes, Energy metabolism, Glucose metabolism disorders, PFKM, Zebrafish
MeSH Terms
  • Animals
  • Energy Metabolism*/genetics
  • Energy Metabolism*/physiology
  • Gene Knockout Techniques
  • Glucose*/metabolism
  • Phosphofructokinases*/genetics
  • Phosphofructokinases*/metabolism
  • Zebrafish/genetics
  • Zebrafish/metabolism
  • Zebrafish Proteins*/genetics
  • Zebrafish Proteins*/metabolism
PubMed
40712841 Full text @ Gen. Comp. Endocrinol.
Abstract
In our previous study, Phosphofructokinase, muscle (PFKM), a key enzyme in glucose metabolism, was found to be decreased in the urinary exosomes of diabetic patients. The role of PFKM in glucose and energy metabolism is not fully understood. The study explores PFKM's implications in these metabolic pathways through the lens of a zebrafish model.
We analyzed pfkma and pfkmb expressions in early zebrafish development using Daniocell and ZESTA databases and performed whole-mount in situ hybridization on embryos up to four days old. The CRISPR/Cas9 system was utilized to create pfkma and pfkmb knockout zebrafish, and qRT-PCR measured the expression of various genes, including β-actin, pfkma, pfkmb, peo1, mfn1, drp1, nd2, cytb, cox3, and atp6, in the embryos.
Knockout mutants displayed elevated glucose levels across whole embryos. Additionally, at 5 days post-fertilization (dpf), pfkma and pfkmb double mutants showed pancreatic islet proliferation, a decrease in ATP levels, a reduction in the expression of the mitochondrial-related gene peo1, and reduced locomotor activity.
PFKM plays an important role in stabilizing glucose metabolism and has a certain impact on mitochondrial energy metabolism pathways in zebrafish model.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping