<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bohr T</submitter><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><pagination>233-42</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4621841</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>211(2)</volume><pubmed_abstract>Homologue synapsis is required for meiotic chromosome segregation, but how synapsis is initiated between chromosomes is poorly understood. In Caenorhabditis elegans, synapsis and a checkpoint that monitors synapsis depend on pairing centers (PCs), cis-acting loci that interact with nuclear envelope proteins, such as SUN-1, to access cytoplasmic microtubules. Here, we report that spindle assembly checkpoint (SAC) components MAD-1, MAD-2, and BUB-3 are required to negatively regulate synapsis and promote the synapsis checkpoint response. Both of these roles are independent of a conserved component of the anaphase-promoting complex, indicating a unique role for these proteins in meiotic prophase. MAD-1 and MAD-2 localize to the periphery of meiotic nuclei and interact with SUN-1, suggesting a</pubmed_abstract><journal>The Journal of cell biology</journal><pubmed_title>Spindle assembly checkpoint proteins regulate and monitor meiotic synapsis in C. elegans.</pubmed_title><pmcid>PMC4621841</pmcid><funding_grant_id>R01GM097144</funding_grant_id><funding_grant_id>T32 GM008646</funding_grant_id><funding_grant_id>R01 GM097144</funding_grant_id><funding_grant_id>P40 OD010440</funding_grant_id><funding_grant_id>T32GM008646</funding_grant_id><funding_grant_id>R25 GM058903</funding_grant_id><pubmed_authors>Bhalla N</pubmed_authors><pubmed_authors>Bohr T</pubmed_authors><pubmed_authors>Klee E</pubmed_authors><pubmed_authors>Nelson CR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Spindle assembly checkpoint proteins regulate and monitor meiotic synapsis in C. elegans.</name><description>Homologue synapsis is required for meiotic chromosome segregation, but how synapsis is initiated between chromosomes is poorly understood. In Caenorhabditis elegans, synapsis and a checkpoint that monitors synapsis depend on pairing centers (PCs), cis-acting loci that interact with nuclear envelope proteins, such as SUN-1, to access cytoplasmic microtubules. Here, we report that spindle assembly checkpoint (SAC) components MAD-1, MAD-2, and BUB-3 are required to negatively regulate synapsis and promote the synapsis checkpoint response. Both of these roles are independent of a conserved component of the anaphase-promoting complex, indicating a unique role for these proteins in meiotic prophase. MAD-1 and MAD-2 localize to the periphery of meiotic nuclei and interact with SUN-1, suggesting a</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Oct</publication><modification>2025-04-06T19:45:20.461Z</modification><creation>2019-03-27T02:00:49Z</creation></dates><accession>S-EPMC4621841</accession><cross_references><pubmed>26483555</pubmed><doi>10.1083/jcb.201409035</doi></cross_references></HashMap>