<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Insley P</submitter><funding>National Institute of Neurological Disorders and Stroke</funding><funding>NINDS NIH HHS</funding><funding>NIH HHS</funding><funding>National Institute of Child Health and Human Development</funding><pagination>e0194861</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5874040</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(3)</volume><pubmed_abstract>The Caenorhabditis elegans cell lineage is nearly invariant. Whether this stereotyped cell-division pattern promotes reproducibility in cell shapes/positions is not generally known, as manual spatiotemporal cell-shape/position alignments are labor-intensive, and fully-automated methods are not described. Here, we report automated algorithms for spatiotemporal alignments of C. elegans embryos from pre-morphogenesis to motor-activity initiation. We use sparsely-labeled green-fluorescent nuclei and a pan-nuclear red-fluorescent reporter to register consecutive imaging time points and compare embryos. Using our method, we monitor early assembly of the nerve-ring (NR) brain neuropil. While NR pioneer neurons exhibit reproducible growth kinetics and axon positions, cell-body placements are variable. Thus, pioneer-neuron axon locations, but not cell-body positions, are under selection. We also show that anterior NR displacement in cam-1/ROR Wnt-receptor mutants is not an early NR assembly defect. Our results demonstrate the utility of automated spatiotemporal alignments of C. elegans embryos, and uncover key principles guiding nervous-system development in this animal.</pubmed_abstract><journal>PloS one</journal><pubmed_title>Automated C. elegans embryo alignments reveal brain neuropil position invariance despite lax cell body placement.</pubmed_title><pmcid>PMC5874040</pmcid><funding_grant_id>NS081490</funding_grant_id><funding_grant_id>R35 NS105094</funding_grant_id><funding_grant_id>R01NS064273</funding_grant_id><funding_grant_id>HD078703</funding_grant_id><funding_grant_id>R35NS105094</funding_grant_id><funding_grant_id>NS095795</funding_grant_id><funding_grant_id>R01NS095795</funding_grant_id><funding_grant_id>R01HD078703</funding_grant_id><funding_grant_id>NS064273</funding_grant_id><funding_grant_id>R01NS081490</funding_grant_id><pubmed_authors>Insley P</pubmed_authors><pubmed_authors>Shaham S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Automated C. elegans embryo alignments reveal brain neuropil position invariance despite lax cell body placement.</name><description>The Caenorhabditis elegans cell lineage is nearly invariant. Whether this stereotyped cell-division pattern promotes reproducibility in cell shapes/positions is not generally known, as manual spatiotemporal cell-shape/position alignments are labor-intensive, and fully-automated methods are not described. Here, we report automated algorithms for spatiotemporal alignments of C. elegans embryos from pre-morphogenesis to motor-activity initiation. We use sparsely-labeled green-fluorescent nuclei and a pan-nuclear red-fluorescent reporter to register consecutive imaging time points and compare embryos. Using our method, we monitor early assembly of the nerve-ring (NR) brain neuropil. While NR pioneer neurons exhibit reproducible growth kinetics and axon positions, cell-body placements are variable. Thus, pioneer-neuron axon locations, but not cell-body positions, are under selection. We also show that anterior NR displacement in cam-1/ROR Wnt-receptor mutants is not an early NR assembly defect. Our results demonstrate the utility of automated spatiotemporal alignments of C. elegans embryos, and uncover key principles guiding nervous-system development in this animal.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2024-12-04T00:32:55.163Z</modification><creation>2019-03-26T23:25:58Z</creation></dates><accession>S-EPMC5874040</accession><cross_references><pubmed>29590193</pubmed><doi>10.1371/journal.pone.0194861</doi></cross_references></HashMap>