Review Article

Genetic Rodent Models of Amyotrophic Lateral Sclerosis

Table 3

Overview of transgenic mouse models for motor neuron degeneration (atypical or rare FALS and candidate genes).

DiseaseGene productInheritanceAnimalGenetic modificationReference

ALS2AlsinRecessiveMouseKO (exon 3) [50]
        KO (stop codon in exon 3) [51]
KO (exon 3 and 4) [52]
KO (exon 4) [53]
ALS8VAPBDominantMousePrP; VAPB P56S [54]
ALSDynactinDominantMouseKnock-in G59S p150Glued[55]
Thy-1; G59 p150Glued [56, 57]
CMT2E/1FNeurofilament-LDominantMouseNF-L L394P[58]
NAPeripherinNAMouseoverexpression[59]
NAVascular endothelial growth factorNAMouseVEGFδ/δ [60]
FTDP-tautauDominantMouse4R human tau [61]
        R406W human tau[62, 63]
P301L human tau [64]
G272V, P301S human tau [65]
V337M human tau [66]
P301S human tau [67]

PrP: prion promoter, CMT: Charcot-Marie-Tooth, FTDP: frontotemporal dementia with parkinsonism, and NA: not available.