Lee, D., Jeong, H.C., Kim, S.Y., Chung, J.Y., Cho, S.H., Kim, K.A., Cho, J.H., Ko, B.S., Cha, I.J., Chung, C.G., Kim, E.S., Lee, S.B. (2024). A comparison study of pathological features and drug efficacy between Drosophila models of C9orf72 ALS/FTD.  Mol. Cells 47(1): 100005.

FBrf0258792

Research paper

Amyotrophic lateral sclerosis is a devastating neurodegenerative disease with a complex genetic basis, presenting both in familial and sporadic forms. The hexanucleotide (G4C2) repeat expansion in the C9orf72 gene, which triggers distinct pathogenic mechanisms, has been identified as a major contributor to familial and sporadic Amyotrophic lateral sclerosis cases. Animal models have proven pivotal in understanding these mechanisms; however, discrepancies between models due to variable transgene sequence, expression levels, and toxicity profiles complicate the translation of findings. Herein, we provide a systematic comparison of 7 publicly available Drosophila transgenes modeling the G4C2 expansion under uniform conditions, evaluating variations in their toxicity profiles. Further, we tested 3 previously characterized disease-modifying drugs in selected lines to uncover discrepancies among the tested strains. Our study not only deepens our understanding of the C9orf72 G4C2 mutations but also presents a framework for comparing constructs with minute structural differences. This work may be used to inform experimental designs to better model disease mechanisms and help guide the development of targeted interventions for neurodegenerative diseases, thus bridging the gap between model-based research and therapeutic application.

PMC10880080 (PMC) (EuropePMC)