Zinc finger motifs are distributed amongst many eukaryotic protein families,
directing nucleic acid-protein and protein-protein interactions. Zinc finger
protein 106 (ZFP106) has previously been associated with roles in immune
response, muscle differentiation, testes development and DNA damage, although
little is known about its specific function. To further investigate the function
of ZFP106, we performed an in-depth characterization of Zfp106 deficient mice
(Zfp106(-/-)), and we report a novel role for ZFP106 in motor and sensory
neuronal maintenance and survival. Zfp106(-/-) mice develop severe motor
abnormalities, major deficits in muscle strength and histopathological changes in
muscle. Intriguingly, despite being highly expressed throughout the central
nervous system, Zfp106(-/-) mice undergo selective motor and sensory neuronal and
axonal degeneration specific to the spinal cord and peripheral nervous system.
Neurodegeneration does not occur during development of Zfp106(-/-) mice,
suggesting that ZFP106 is likely required for the maintenance of mature
peripheral motor and sensory neurons. Analysis of embryonic Zfp106(-/-) motor
neurons revealed deficits in mitochondrial function, with an inhibition of
Complex I within the mitochondrial electron transport chain. Our results
highlight a vital role for ZFP106 in sensory and motor neuron maintenance and
reveal a novel player in mitochondrial dysfunction and neurodegeneration.
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Zinc finger motifs are distributed amongst many eukaryotic protein families,
directing nucleic acid-protein and protein-protein interactions. Zinc finger
protein 106 (ZFP106) has previously been associated with roles in immune
response, muscle differentiation, testes development and DNA damage, although
little is known about its specific function. To further investigate the function
of ZFP106, we performed an in-depth characterization of Zfp106 deficient mice
(Zfp106(-/-)), and we report...
»