M S Borges, M M A Salles, E F Oliveira, F M Magalhães, D C Silva, H F M Oliveira, K C Faria, V N Laine, T M Lilley, J M Silva, F M C B Domingos
{"title":"Gene-Specific Substitution Rates for the Vespertilionidae (Chiroptera: Mammalia) Mitochondrial Genome, with the Description of Three new Mitogenomes.","authors":"M S Borges, M M A Salles, E F Oliveira, F M Magalhães, D C Silva, H F M Oliveira, K C Faria, V N Laine, T M Lilley, J M Silva, F M C B Domingos","doi":"10.1007/s00239-025-10265-5","DOIUrl":null,"url":null,"abstract":"<p><p>Molecular data are irreplaceable resources for reconstructing the tree of life. Gene-specific substitution rates are essential for estimating divergence times in the absence of fossil calibration or converting coalescent units into absolute time in phylogeographic approaches, among other uses. However, substitution rate estimates are often derived from limited genomic loci, narrow taxonomic comparisons, and model organisms, hindering their applicability to understudied taxa. Among mammals, bats (Order Chiroptera)-despite their ecological diversity and evolutionary significance-remain underrepresented in substitution rate studies, particularly within the family Vespertilionidae, the third largest mammal family. Here, we investigate mitochondrial genome (mitogenome) evolutionary rates in this group, while also describing the first complete mitogenomes of three Neoeptesicus species: N. brasiliensis, N. diminutus, and N. furinalis. Using fossil-calibrated Bayesian phylogenetic analyses, we estimated that protein-coding genes evolve at rates between 0.0055-0.0089 substitutions per site per million years (subs/site/Ma), while ribosomal RNA genes evolve at rates between 0.0035-0.0049 subs/site/Ma. Notably, the ND4, ND4L, and ND5 genes exhibited the highest rates, whereas non-coding regions showed the lowest, suggesting that gene-specific evolutionary constraints influence these rates. These findings provide the first comprehensive substitution rate framework for Vespertilionidae mitogenomes, addressing a critical gap in genomic resources for this taxonomically complex group. By integrating novel mitogenomic data with rigorous rate estimation, this study advances our capacity to resolve evolutionary patterns in bats, offering a benchmark for future phylogenetic and phylogeographic studies in non-model mammals.</p>","PeriodicalId":16366,"journal":{"name":"Journal of Molecular Evolution","volume":" ","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Evolution","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s00239-025-10265-5","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Molecular data are irreplaceable resources for reconstructing the tree of life. Gene-specific substitution rates are essential for estimating divergence times in the absence of fossil calibration or converting coalescent units into absolute time in phylogeographic approaches, among other uses. However, substitution rate estimates are often derived from limited genomic loci, narrow taxonomic comparisons, and model organisms, hindering their applicability to understudied taxa. Among mammals, bats (Order Chiroptera)-despite their ecological diversity and evolutionary significance-remain underrepresented in substitution rate studies, particularly within the family Vespertilionidae, the third largest mammal family. Here, we investigate mitochondrial genome (mitogenome) evolutionary rates in this group, while also describing the first complete mitogenomes of three Neoeptesicus species: N. brasiliensis, N. diminutus, and N. furinalis. Using fossil-calibrated Bayesian phylogenetic analyses, we estimated that protein-coding genes evolve at rates between 0.0055-0.0089 substitutions per site per million years (subs/site/Ma), while ribosomal RNA genes evolve at rates between 0.0035-0.0049 subs/site/Ma. Notably, the ND4, ND4L, and ND5 genes exhibited the highest rates, whereas non-coding regions showed the lowest, suggesting that gene-specific evolutionary constraints influence these rates. These findings provide the first comprehensive substitution rate framework for Vespertilionidae mitogenomes, addressing a critical gap in genomic resources for this taxonomically complex group. By integrating novel mitogenomic data with rigorous rate estimation, this study advances our capacity to resolve evolutionary patterns in bats, offering a benchmark for future phylogenetic and phylogeographic studies in non-model mammals.
期刊介绍:
Journal of Molecular Evolution covers experimental, computational, and theoretical work aimed at deciphering features of molecular evolution and the processes bearing on these features, from the initial formation of macromolecular systems through their evolution at the molecular level, the co-evolution of their functions in cellular and organismal systems, and their influence on organismal adaptation, speciation, and ecology. Topics addressed include the evolution of informational macromolecules and their relation to more complex levels of biological organization, including populations and taxa, as well as the molecular basis for the evolution of ecological interactions of species and the use of molecular data to infer fundamental processes in evolutionary ecology. This coverage accommodates such subfields as new genome sequences, comparative structural and functional genomics, population genetics, the molecular evolution of development, the evolution of gene regulation and gene interaction networks, and in vitro evolution of DNA and RNA, molecular evolutionary ecology, and the development of methods and theory that enable molecular evolutionary inference, including but not limited to, phylogenetic methods.