<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Schaeffer J</submitter><funding>European Research Council</funding><pagination>2881-2898.e12</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10522804</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>111(18)</volume><pubmed_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</pubmed_abstract><journal>Neuron</journal><pubmed_title>Customization of the translational complex regulates mRNA-specific translation to control CNS regeneration.</pubmed_title><pmcid>PMC10522804</pmcid><funding_grant_id>759089</funding_grant_id><pubmed_authors>Diaz JJ</pubmed_authors><pubmed_authors>Nawabi H</pubmed_authors><pubmed_authors>Vilallongue N</pubmed_authors><pubmed_authors>Catez F</pubmed_authors><pubmed_authors>Schaeffer J</pubmed_authors><pubmed_authors>El Bakdouri N</pubmed_authors><pubmed_authors>Decourt C</pubmed_authors><pubmed_authors>Plissonnier E</pubmed_authors><pubmed_authors>Excoffier B</pubmed_authors><pubmed_authors>Saudou F</pubmed_authors><pubmed_authors>Blot B</pubmed_authors><pubmed_authors>Humbert S</pubmed_authors><pubmed_authors>Belin S</pubmed_authors><pubmed_authors>Paccard A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Customization of the translational complex regulates mRNA-specific translation to control CNS regeneration.</name><description>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</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Sep</publication><modification>2026-05-29T02:05:19.25Z</modification><creation>2025-04-05T09:59:36.931Z</creation></dates><accession>S-EPMC10522804</accession><cross_references><pubmed>37442131</pubmed><doi>10.1016/j.neuron.2023.06.005</doi></cross_references></HashMap>