<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Trevisan AJ</submitter><funding>NINDS NIH HHS</funding><funding>NCI NIH HHS</funding><pubmed_abstract>Neural circuits in the spinal cord are composed of diverse sets of interneurons that play crucial roles in shaping motor output. Despite progress in revealing the cellular architecture of the spinal cord, the extent of cell type heterogeneity within interneuron populations remains unclear. Here, we present a single-nucleus transcriptomic atlas of spinal V1 interneurons across postnatal development. We find that the core molecular taxonomy distinguishing neonatal V1 interneurons perdures into adulthood, suggesting conservation of function across development. Moreover, we identify a key role for En1, a transcription factor that marks the V1 population, in specifying one unique subset of V1&lt;sup>Pou6f2&lt;/sup> interneurons. Loss of En1 selectively disrupts the frequency of rhythmic locomotor out</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2024.09.18.613279</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11429899</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The transcriptomic landscape of spinal V1 interneurons reveals a role for En1 in specific elements of motor output.</pubmed_title><pmcid>PMC11429899</pmcid><funding_grant_id>P30 CA021765</funding_grant_id><funding_grant_id>R01 NS123116</funding_grant_id><pubmed_authors>Menon V</pubmed_authors><pubmed_authors>Han K</pubmed_authors><pubmed_authors>Hinton JM</pubmed_authors><pubmed_authors>Gatto G</pubmed_authors><pubmed_authors>Ramirez C</pubmed_authors><pubmed_authors>Chapman P</pubmed_authors><pubmed_authors>Gabitto MI</pubmed_authors><pubmed_authors>Trevisan AJ</pubmed_authors><pubmed_authors>Kulkarni AS</pubmed_authors><pubmed_authors>Klein I</pubmed_authors><pubmed_authors>Bikoff JB</pubmed_authors></additional><is_claimable>false</is_claimable><name>The transcriptomic landscape of spinal V1 interneurons reveals a role for En1 in specific elements of motor output.</name><description>Neural circuits in the spinal cord are composed of diverse sets of interneurons that play crucial roles in shaping motor output. Despite progress in revealing the cellular architecture of the spinal cord, the extent of cell type heterogeneity within interneuron populations remains unclear. Here, we present a single-nucleus transcriptomic atlas of spinal V1 interneurons across postnatal development. We find that the core molecular taxonomy distinguishing neonatal V1 interneurons perdures into adulthood, suggesting conservation of function across development. Moreover, we identify a key role for En1, a transcription factor that marks the V1 population, in specifying one unique subset of V1&lt;sup>Pou6f2&lt;/sup> interneurons. Loss of En1 selectively disrupts the frequency of rhythmic locomotor out</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-05-29T03:17:11.275Z</modification><creation>2025-04-04T02:33:16.765Z</creation></dates><accession>S-EPMC11429899</accession><cross_references><pubmed>39345580</pubmed><doi>10.1101/2024.09.18.613279</doi></cross_references></HashMap>