<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mason MRJ</submitter><funding>Van den Houtenfonds; the International Spinal Research Trust</funding><funding>The Francis Crick Institute</funding><funding>Dutch Research Council (NWO)</funding><funding>ZonMw</funding><funding>International Foundation for Research in Paraplegia</funding><pagination>1242-1262</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9029231</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31(8)</volume><pubmed_abstract>The regeneration-associated gene (RAG) expression program is activated in injured peripheral neurons after axotomy and enables long-distance axon re-growth. Over 1000 genes are regulated, and many transcription factors are upregulated or activated as part of this response. However, a detailed picture of how RAG expression is regulated is lacking. In particular, the transcriptional targets and specific functions of the various transcription factors are unclear. Jun was the first-regeneration-associated transcription factor identified and the first shown to be functionally important. Here we fully define the role of Jun in the RAG expression program in regenerating facial motor neurons. At 1, 4 and 14 days after axotomy, Jun upregulates 11, 23 and 44% of the RAG program, respectively. Jun fu</pubmed_abstract><journal>Human molecular genetics</journal><pubmed_title>The Jun-dependent axon regeneration gene program: Jun promotes regeneration over plasticity.</pubmed_title><pmcid>PMC9029231</pmcid><funding_grant_id>91211043</funding_grant_id><funding_grant_id>STR 111</funding_grant_id><funding_grant_id>10039</funding_grant_id><funding_grant_id>IRP-NL-011/05</funding_grant_id><pubmed_authors>Behrens A</pubmed_authors><pubmed_authors>Wolzak K</pubmed_authors><pubmed_authors>Raivich G</pubmed_authors><pubmed_authors>Mason MRJ</pubmed_authors><pubmed_authors>Verhaagen J</pubmed_authors><pubmed_authors>van Erp S</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Jun-dependent axon regeneration gene program: Jun promotes regeneration over plasticity.</name><description>The regeneration-associated gene (RAG) expression program is activated in injured peripheral neurons after axotomy and enables long-distance axon re-growth. Over 1000 genes are regulated, and many transcription factors are upregulated or activated as part of this response. However, a detailed picture of how RAG expression is regulated is lacking. In particular, the transcriptional targets and specific functions of the various transcription factors are unclear. Jun was the first-regeneration-associated transcription factor identified and the first shown to be functionally important. Here we fully define the role of Jun in the RAG expression program in regenerating facial motor neurons. At 1, 4 and 14 days after axotomy, Jun upregulates 11, 23 and 44% of the RAG program, respectively. Jun fu</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2026-07-14T17:08:55.934Z</modification><creation>2025-04-04T07:46:07.004Z</creation></dates><accession>S-EPMC9029231</accession><cross_references><pubmed>34718572</pubmed><doi>10.1093/hmg/ddab315</doi></cross_references></HashMap>