<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Beiriger A</submitter><funding>National Center for Advancing Translational Sciences</funding><funding>NICHD NIH HHS</funding><funding>NCATS NIH HHS</funding><funding>National Science Foundation</funding><pagination>1293-1307</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8238524</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>529(7)</volume><pubmed_abstract>In vertebrate animals, motor and sensory efferent neurons carry information from the central nervous system (CNS) to peripheral targets. These two types of efferent systems sometimes bear a close resemblance, sharing common segmental organization, axon pathways, and chemical messengers. Here, we focus on the development of the octavolateral efferent neurons (OENs) and their interactions with the closely-related facial branchiomotor neurons (FBMNs) in zebrafish. Using live-imaging approaches, we investigate the birth, migration, and projection patterns of OENs. We find that OENs are born in two distinct groups: a group of rostral efferent neurons (RENs) that arises in the fourth segment, or rhombomere (r4), of the hindbrain and a group of caudal efferent neurons (CENs) that arises in r5. Both RENs and CENs then migrate posteriorly through the hindbrain between 18 and 48 hrs postfertilization, alongside the r4-derived FBMNs. Like the FBMNs, migration of the r4-derived RENs depends on function of the segmental identity gene hoxb1a; unlike the FBMNs, however, both OEN populations move independently of prickle1b. Further, we investigate whether the previously described "pioneer" neuron that leads FBMN migration through the hindbrain is an r4-derived FBMN/REN or an r5-derived CEN. Our experiments verify that the pioneer is an r4-derived neuron and reaffirm its role in leading FBMN migration across the r4/5 border. In contrast, the r5-derived CENs migrate independently of the pioneer. Together, these results indicate that the mechanisms OENs use to navigate the hindbrain differ significantly from those employed by FBMNs.</pubmed_abstract><journal>The Journal of comparative neurology</journal><pubmed_title>Development and migration of the zebrafish rhombencephalic octavolateral efferent neurons.</pubmed_title><pmcid>PMC8238524</pmcid><funding_grant_id>T32 HD055164</funding_grant_id><funding_grant_id>1528911</funding_grant_id><funding_grant_id>UL1 TR002389</funding_grant_id><funding_grant_id>5UL1TR002389</funding_grant_id><funding_grant_id>DGE‐1144082</funding_grant_id><pubmed_authors>Beiriger A</pubmed_authors><pubmed_authors>Prince V</pubmed_authors><pubmed_authors>Singh N</pubmed_authors><pubmed_authors>Narayan S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development and migration of the zebrafish rhombencephalic octavolateral efferent neurons.</name><description>In vertebrate animals, motor and sensory efferent neurons carry information from the central nervous system (CNS) to peripheral targets. These two types of efferent systems sometimes bear a close resemblance, sharing common segmental organization, axon pathways, and chemical messengers. Here, we focus on the development of the octavolateral efferent neurons (OENs) and their interactions with the closely-related facial branchiomotor neurons (FBMNs) in zebrafish. Using live-imaging approaches, we investigate the birth, migration, and projection patterns of OENs. We find that OENs are born in two distinct groups: a group of rostral efferent neurons (RENs) that arises in the fourth segment, or rhombomere (r4), of the hindbrain and a group of caudal efferent neurons (CENs) that arises in r5. Both RENs and CENs then migrate posteriorly through the hindbrain between 18 and 48 hrs postfertilization, alongside the r4-derived FBMNs. Like the FBMNs, migration of the r4-derived RENs depends on function of the segmental identity gene hoxb1a; unlike the FBMNs, however, both OEN populations move independently of prickle1b. Further, we investigate whether the previously described "pioneer" neuron that leads FBMN migration through the hindbrain is an r4-derived FBMN/REN or an r5-derived CEN. Our experiments verify that the pioneer is an r4-derived neuron and reaffirm its role in leading FBMN migration across the r4/5 border. In contrast, the r5-derived CENs migrate independently of the pioneer. Together, these results indicate that the mechanisms OENs use to navigate the hindbrain differ significantly from those employed by FBMNs.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2025-06-01T03:29:14.445Z</modification><creation>2025-06-01T03:29:14.445Z</creation></dates><accession>S-EPMC8238524</accession><cross_references><pubmed>32869305</pubmed><doi>10.1002/cne.25021</doi></cross_references></HashMap>