RARS1 integration into the multisynthetase complex is crucial for mammalian brain development

Abstract

Aminoacyl tRNA synthetases occupy a central role in protein synthesis by charging tRNAs with their cognate amino acid. Eight aminoacyl-tRNA synthetases with nine enzymatic activities form a large protein complex but the breadth of functions mediated by the multisynthetase complex remains elusive. Neurological disorders have been associated with mutations within the domain tethering Arginyl-tRNA synthetase (RARS1) to the multisynthetase complex, which offers an interesting bridge between protein synthesis and neurodevelopment. To interrogate this connection, we developed a mouse model where RARS1 is excluded from the multisynthetase complex in the forebrain. We observed profound disruptions in neural development as attested by drastically reduced forebrain size and behavioral deficits. At the molecular level, neurodevelopmental and ribosomal genes were dysregulated. Finally, the subcellular localization of RARS1 and its colocalization with other translational machinery components were perturbed. Altogether, our results reveal the necessity of RARS1 integration in the multisynthetase complex for proper neurodevelopment.