<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zerbes RM</submitter><funding>Deutsche Forschungsgemeinschaft (DFG)</funding><funding>Excellence Initiative of the German Federal and State Governments</funding><funding>European Research Council</funding><funding>Deutsche Forschungsgemeinschaft</funding><pagination>353-384</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11772845</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(2)</volume><pubmed_abstract>The boundary and cristae domains of the mitochondrial inner membrane are connected by crista junctions. Most cristae membrane proteins are nuclear-encoded and inserted by the mitochondrial protein import machinery into the inner boundary membrane. Thus, they must overcome the diffusion barrier imposed by crista junctions to reach their final location. Here, we show that respiratory chain complexes and assembly intermediates are physically connected to the mitochondrial contact site and cristae organizing system (MICOS) that is essential for the formation and stability of crista junctions. We identify the inner membrane protein Mar26 (Fmp10) as a determinant in the biogenesis of the cytochrome bc&lt;sub>1&lt;/sub> complex (complex III). Mar26 couples a Rieske Fe/S protein-containing assembly inte</pubmed_abstract><journal>EMBO reports</journal><pubmed_title>Coordination of cytochrome bc&amp;lt;sub&amp;gt;1&amp;lt;/sub&amp;gt; complex assembly at MICOS.</pubmed_title><pmcid>PMC11772845</pmcid><funding_grant_id>CIBSS - EXC-2189 - project ID 390939984</funding_grant_id><funding_grant_id>Consolidator Grant 648235</funding_grant_id><funding_grant_id>BIOSS - EXC-294</funding_grant_id><funding_grant_id>SFB 894 - project ID 157660137</funding_grant_id><funding_grant_id>648235</funding_grant_id><funding_grant_id>FOR 2848 - project ID 401510699</funding_grant_id><funding_grant_id>SFB 746 - project ID 26068018</funding_grant_id><pubmed_authors>van der Laan M</pubmed_authors><pubmed_authors>Klar RFU</pubmed_authors><pubmed_authors>Rampelt H</pubmed_authors><pubmed_authors>Perschil I</pubmed_authors><pubmed_authors>Bohnert M</pubmed_authors><pubmed_authors>Oeljeklaus S</pubmed_authors><pubmed_authors>de Boer R</pubmed_authors><pubmed_authors>Peikert CD</pubmed_authors><pubmed_authors>von der Malsburg K</pubmed_authors><pubmed_authors>Mehnert CS</pubmed_authors><pubmed_authors>Zerbes RM</pubmed_authors><pubmed_authors>Kram A</pubmed_authors><pubmed_authors>van der Klei I</pubmed_authors><pubmed_authors>Warscheid B</pubmed_authors><pubmed_authors>Colina-Tenorio L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Coordination of cytochrome bc&amp;lt;sub&amp;gt;1&amp;lt;/sub&amp;gt; complex assembly at MICOS.</name><description>The boundary and cristae domains of the mitochondrial inner membrane are connected by crista junctions. Most cristae membrane proteins are nuclear-encoded and inserted by the mitochondrial protein import machinery into the inner boundary membrane. Thus, they must overcome the diffusion barrier imposed by crista junctions to reach their final location. Here, we show that respiratory chain complexes and assembly intermediates are physically connected to the mitochondrial contact site and cristae organizing system (MICOS) that is essential for the formation and stability of crista junctions. We identify the inner membrane protein Mar26 (Fmp10) as a determinant in the biogenesis of the cytochrome bc&lt;sub>1&lt;/sub> complex (complex III). Mar26 couples a Rieske Fe/S protein-containing assembly inte</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2025-04-04T23:11:14.9Z</modification><creation>2025-04-04T23:11:14.9Z</creation></dates><accession>S-EPMC11772845</accession><cross_references><pubmed>39623166</pubmed><doi>10.1038/s44319-024-00336-x</doi></cross_references></HashMap>