<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17</volume><submitter>Day JL</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The Anaphase Promoting Complex (APC/C), an E3 ubiquitin ligase, plays a key role in cell cycle control, but it is also thought to operate in postmitotic neurons. Most studies linking APC/C function to neuron biology employed perturbations of the APC/C activators, cell division cycle protein 20 (Cdc20) and Cdc20 homologue 1 (Cdh1). However, multiple lines of evidence indicate that Cdh1 and Cdc20 can function in APC/C-independent contexts, so that the effects of their perturbation cannot strictly be linked to APC/C function.&lt;h4>Methods&lt;/h4>We therefore deleted the gene encoding Anaphase Promoting Complex 4 (APC4), a core APC/C component, in neurons cultured from conditional knockout (cKO) mice.&lt;h4>Results&lt;/h4>Our data indicate that several previously published substrates</pubmed_abstract><journal>Frontiers in molecular neuroscience</journal><pagination>1352782</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11199872</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Deletion of a core APC/C component reveals APC/C function in regulating neuronal USP1 levels and morphology.</pubmed_title><pmcid>PMC11199872</pmcid><pubmed_authors>Day JL</pubmed_authors><pubmed_authors>Tirard M</pubmed_authors><pubmed_authors>Brose N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Deletion of a core APC/C component reveals APC/C function in regulating neuronal USP1 levels and morphology.</name><description>&lt;h4>Introduction&lt;/h4>The Anaphase Promoting Complex (APC/C), an E3 ubiquitin ligase, plays a key role in cell cycle control, but it is also thought to operate in postmitotic neurons. Most studies linking APC/C function to neuron biology employed perturbations of the APC/C activators, cell division cycle protein 20 (Cdc20) and Cdc20 homologue 1 (Cdh1). However, multiple lines of evidence indicate that Cdh1 and Cdc20 can function in APC/C-independent contexts, so that the effects of their perturbation cannot strictly be linked to APC/C function.&lt;h4>Methods&lt;/h4>We therefore deleted the gene encoding Anaphase Promoting Complex 4 (APC4), a core APC/C component, in neurons cultured from conditional knockout (cKO) mice.&lt;h4>Results&lt;/h4>Our data indicate that several previously published substrates</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2025-04-18T12:24:12.226Z</modification><creation>2024-10-15T14:20:57.597Z</creation></dates><accession>S-EPMC11199872</accession><cross_references><pubmed>38932933</pubmed><doi>10.3389/fnmol.2024.1352782</doi></cross_references></HashMap>