<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Okafornta CW</submitter><funding>NIH HHS</funding><pubmed_abstract>How embryos adapt their internal cellular machinery to reductions in cell size during development remains a fundamental question in cell biology&lt;sup>1-11&lt;/sup>. Here, we use high-resolution lattice light-sheet fluorescence microscopy and automated image analysis to quantify lineage-resolved mitotic spindle and chromosome segregation dynamics from the 2- to 64-cell stages in &lt;i>Caenorhabditis elegans&lt;/i> embryos. While spindle length scales with cell size across both wild-type and size-perturbed embryos, chromosome segregation dynamics remain largely invariant, suggesting that distinct mechanisms govern these mitotic processes. Combining femtosecond laser ablation&lt;sup>12,13&lt;/sup> with large-scale electron tomography&lt;sup>14&lt;/sup>, we find that central spindle microtubules mediate chromosome </pubmed_abstract><journal>Research square</journal><pagination>rs.3.rs-7923379</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12687828</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cell size reduction scales spindle elongation but not chromosome segregation in &amp;lt;i&amp;gt;C. elegans&amp;lt;/i&amp;gt;.</pubmed_title><pmcid>PMC12687828</pmcid><funding_grant_id>P40 OD010440</funding_grant_id><pubmed_authors>Farhadifar R</pubmed_authors><pubmed_authors>Okafornta CW</pubmed_authors><pubmed_authors>Muller-Reichert T</pubmed_authors><pubmed_authors>Baum D</pubmed_authors><pubmed_authors>Needleman DJ</pubmed_authors><pubmed_authors>Kockert M</pubmed_authors><pubmed_authors>Fabig G</pubmed_authors><pubmed_authors>Wu HY</pubmed_authors><pubmed_authors>Vogel M</pubmed_authors><pubmed_authors>Haase R</pubmed_authors><pubmed_authors>Shelley MJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cell size reduction scales spindle elongation but not chromosome segregation in &amp;lt;i&amp;gt;C. elegans&amp;lt;/i&amp;gt;.</name><description>How embryos adapt their internal cellular machinery to reductions in cell size during development remains a fundamental question in cell biology&lt;sup>1-11&lt;/sup>. Here, we use high-resolution lattice light-sheet fluorescence microscopy and automated image analysis to quantify lineage-resolved mitotic spindle and chromosome segregation dynamics from the 2- to 64-cell stages in &lt;i>Caenorhabditis elegans&lt;/i> embryos. While spindle length scales with cell size across both wild-type and size-perturbed embryos, chromosome segregation dynamics remain largely invariant, suggesting that distinct mechanisms govern these mitotic processes. Combining femtosecond laser ablation&lt;sup>12,13&lt;/sup> with large-scale electron tomography&lt;sup>14&lt;/sup>, we find that central spindle microtubules mediate chromosome </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-04T03:21:18.695Z</modification><creation>2026-06-04T03:12:44.147Z</creation></dates><accession>S-EPMC12687828</accession><cross_references><pubmed>41377964</pubmed><doi>10.21203/rs.3.rs-7923379/v1</doi></cross_references></HashMap>