The stretcher spontaneous neurodegenerative mutation models Charcot-Marie-Tooth disease type 4D

David Chandler, S. Lopaticki, D. Huang, Michael Hunter, Dora Angelicheva, T. Kilpatrick, R.H.M. King, Luba Kalaydjieva, Grant Morahan

Research output: Contribution to journalArticle

Abstract

Mice affected by a spontaneous mutation which arose within our colony exhibited a neuromuscular phenotype involving tremor and characteristic stretching of the rear limbs. The mutant, named stretcher, was used to breed a backcross cohort for genetic mapping studies. The gene responsible for the mutant phenotype was mapped to a small region on mouse chromosome 15, with a LOD score above 20. Candidate genes within the region included the Ndrg1 gene. Examination of this gene in the mutant mouse strain revealed that exons 10 to 14 had been deleted. Mutations in the human orthologue are known to result in Charcot-Marie-Tooth disease type 4D (CMT4D) a severe early-onset disorder involving Schwann cell dysfunction and extensive demyelination. The stretcher mutant mouse is more severely affected than mice in which the Ndrg1 gene had been knocked out by homologous recombination. Our results demonstrate that the Ndrg1str mutation provides a new model for CMT4D, and demonstrate that exons 10 to 14 of Ndrg1 encode amino acids crucial to the appropriate function of Ndrg1 in the central nervous system.
Original languageEnglish
Article number46
Pages (from-to)1-8
Number of pages8
JournalF1000Research
Volume2
DOIs
Publication statusPublished - 13 May 2013

Fingerprint

Stretchers
Genes
Mutation
Exons
Mutant Strains Mice
Phenotype
Chromosomes, Human, Pair 15
Homologous Recombination
Schwann Cells
Neurology
Demyelinating Diseases
Tremor
Chromosomes
Stretching
Extremities
Central Nervous System
Cells
Hereditary motor and sensory neuropathy, LOM type
Amino Acids

Cite this

Chandler, David ; Lopaticki, S. ; Huang, D. ; Hunter, Michael ; Angelicheva, Dora ; Kilpatrick, T. ; King, R.H.M. ; Kalaydjieva, Luba ; Morahan, Grant. / The stretcher spontaneous neurodegenerative mutation models Charcot-Marie-Tooth disease type 4D. In: F1000Research. 2013 ; Vol. 2. pp. 1-8.
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Chandler, D, Lopaticki, S, Huang, D, Hunter, M, Angelicheva, D, Kilpatrick, T, King, RHM, Kalaydjieva, L & Morahan, G 2013, 'The stretcher spontaneous neurodegenerative mutation models Charcot-Marie-Tooth disease type 4D' F1000Research, vol. 2, 46, pp. 1-8. https://doi.org/10.12688/f1000research.2-46.v1

The stretcher spontaneous neurodegenerative mutation models Charcot-Marie-Tooth disease type 4D. / Chandler, David; Lopaticki, S.; Huang, D.; Hunter, Michael; Angelicheva, Dora; Kilpatrick, T.; King, R.H.M.; Kalaydjieva, Luba; Morahan, Grant.

In: F1000Research, Vol. 2, 46, 13.05.2013, p. 1-8.

Research output: Contribution to journalArticle

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AU - Kilpatrick, T.

AU - King, R.H.M.

AU - Kalaydjieva, Luba

AU - Morahan, Grant

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