UBA1/GARS-dependent pathways drive sensory-motor connectivity defects in spinal muscular atrophy

Hannah Shorrock, Dinja van der Hoorn, Penelope Boyd, Maria del carmen Llavero hurtado, Douglas J. Lamont, B. Wirth, James N Sleigh, G. Schiavone, Thomas Wishart, Ewout Groen, Thomas Gillingwater

Research output: Contribution to journalArticlepeer-review


Deafferentation of motor neurons as a result of defective sensory-motor connectivity is a critical early event in the pathogenesis of spinal muscular atrophy, but the underlying molecular pathways remain unknown. We show that restoration of ubiquitin-like modifier-activating enzyme 1 (UBA1) was sufficient to correct sensory-motor connectivity in the spinal cord of mice with spinal muscular atrophy. Aminoacyl-tRNA synthetases, including GARS, were identified as downstream targets of UBA1. Regulation of GARS by UBA1 occurred via a non-canonical pathway independent of ubiquitylation. Dysregulation of UBA1/GARS pathways in spinal muscular atrophy mice disrupted sensory neuron fate, phenocopying GARS-dependent defects associated with Charcot-Marie-Tooth disease. Sensory neuron fate was corrected following restoration of UBA1 expression and UBA1/GARS pathways in spinal muscular atrophy mice. We conclude that defective sensory motor connectivity in spinal muscular atrophy results from perturbations in a UBA1/GARS pathway that modulates sensory neuron fate, thereby highlighting significant molecular and phenotypic overlap between spinal muscular atrophy and Charcot-Marie-Tooth disease.
Original languageEnglish
Pages (from-to)2878–2894
Issue number10
Early online date25 Sep 2018
Publication statusE-pub ahead of print - 25 Sep 2018

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