<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(7)</volume><submitter>Goncalves LT</submitter><funding>CAPES/PRINT</funding><funding>Conselho Nacional de Desenvolvimento Científico e Tecnológico</funding><funding>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior</funding><pubmed_abstract>Mitochondria play a central role in cellular respiration, but require close coevolution with the nuclear genome for proper function. This process, termed mitonuclear coevolution, is poorly understood on species-level evolutionary timescales, despite its role in speciation. Here, we investigate mitonuclear coevolution in bumblebees (Bombus), a group of ecologically diverse pollinators with rapid mitochondrial (mt) DNA evolution. Leveraging genomic data from a comprehensive set of 55 bumblebee species, we quantified the evolutionary rate correlation (ERC) between mt genes and nuclear genes that interact with mitochondria (N-mt). We found a strong ERC between mt and N-mt genes, but not among mt genes and random nuclear genes, supporting the mitonuclear coevolution hypothesis. Additionally, we</pubmed_abstract><journal>Genome biology and evolution</journal><pagination>evaf123</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12223992</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Mitonuclear Coevolution in Bumblebees (Bombus): Genomic Signatures and Its Role in Climatic Niche Adaptation.</pubmed_title><pmcid>PMC12223992</pmcid><pubmed_authors>Francoso E</pubmed_authors><pubmed_authors>Goncalves LT</pubmed_authors><pubmed_authors>Depra M</pubmed_authors><pubmed_authors>Pezzi PH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mitonuclear Coevolution in Bumblebees (Bombus): Genomic Signatures and Its Role in Climatic Niche Adaptation.</name><description>Mitochondria play a central role in cellular respiration, but require close coevolution with the nuclear genome for proper function. This process, termed mitonuclear coevolution, is poorly understood on species-level evolutionary timescales, despite its role in speciation. Here, we investigate mitonuclear coevolution in bumblebees (Bombus), a group of ecologically diverse pollinators with rapid mitochondrial (mt) DNA evolution. Leveraging genomic data from a comprehensive set of 55 bumblebee species, we quantified the evolutionary rate correlation (ERC) between mt genes and nuclear genes that interact with mitochondria (N-mt). We found a strong ERC between mt and N-mt genes, but not among mt genes and random nuclear genes, supporting the mitonuclear coevolution hypothesis. Additionally, we</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2025-08-14T03:05:49.353Z</modification><creation>2025-08-14T03:05:49.353Z</creation></dates><accession>S-EPMC12223992</accession><cross_references><pubmed>40509913</pubmed><doi>10.1093/gbe/evaf123</doi></cross_references></HashMap>