Customization of the translational complex regulates mRNA-specific translation to control CNS regeneration
Julia Schaeffer, Noémie Vilallongue, Charlotte Decourt, Béatrice Blot, Nacéra El Bakdouri, Elise Plissonnier, Blandine Excoffier, Antoine Paccard, Jean‐Jacques Diaz, Sandrine Humbert, Frédéric Catez, Frédéric Saudou, Homaira Nawabi, Stéphane Belin
Abstract
In the adult mammalian central nervous system (CNS), axons fail to regenerate spontaneously after injury because of a combination of extrinsic and intrinsic factors. Despite recent advances targeting the intrinsic regenerative properties of adult neurons, the molecular mechanisms underlying axon regeneration are not fully understood. Here, we uncover a regulatory mechanism that controls the expression of key proteins involved in regeneration at the translational level. Our results show that mRNA-specific translation is critical for promoting axon regeneration. Indeed, we demonstrate that specific ribosome-interacting proteins, such as the protein Huntingtin (HTT), selectively control the translation of a specific subset of mRNAs. Moreover, modulating the expression of these translationally regulated mRNAs is crucial for promoting axon regeneration. Altogether, our findings highlight that selective translation through the customization of the translational complex is a key mechanism of axon regeneration with major implications in the development of therapeutic strategies for CNS repair.