68P Induced muscle and liver absence of Gne in postnatal mice does not result in structural or functional muscle impairment

• Published in: Neuromuscular disorders : NMD Vol. 43; p. 104441
• Main Authors: Mitrani-Rosenbaum, S., Harazi, A., Yakovlev, L., Ilouz, N., Selke, P., Horstkorte, R., Argov, Z.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.10.2024
• DOI: 10.1016/j.nmd.2024.07.431
• ISSN: 0960-8966

GNE Myopathy is a unique recessive neuromuscular disorder characterized by adult-onset, slowly progressive distal and proximal muscle weakness, caused by mutations in the GNE gene, which is a key enzyme in the biosynthesis of sialic acid. To date, the precise pathophysiology of the disease is not well understood, and no reliable animal model is available. Gne KO is embryonically lethal in mice. To gain insights into GNE function in muscle, we have generated an inducible muscle Gne KO mouse. To minimize the contribution of the liver to the availability of sialic acid to muscle via the serum, we have also induced combined Gne KO in liver and muscle. A mouse carrying loxp sequences flanking Gne exon3 was generated by Crispr/Cas9 and bred with a human skeletal actin (HAS) promoter driven CreERT mouse. Gne muscle knock out was induced by tamoxifen injection of the resulting homozygote GneloxpEx3loxp/HAS Cre mouse. Liver Gne KO was induced by systemic injection of AAV8 vectors carrying the Cre gene driven by the hepatic specific promoter of the thyroxine binding globulin gene. Characterization of these mice for a 12-month period showed no significant changes in their general behaviour, motor performance, muscle mass and structure in spite of a dramatic reduction in sialic acid content in both muscle and liver. We conclude that post weaning lack of Gne and sialic acid in muscle and liver have no pathologic effect in adult mice. These findings could reflect a strong interspecies versatility, but also raise questions about the loss of function hypothesis in Gne Myopathy. If these findings apply to humans they may have a major impact on therapeutic strategies.