Rodents constitute a significant proportion of mammalian diversity, with their adaptability and wide distribution making them indispensable study organisms across various biological disciplines. While the laboratory mouse remains a predominant model rodent, the bank vole (Clethrionomys glareolus) offers a unique perspective as a wild rodent within the large subfamily Arvicolinae. Recognized for its relevance to studynatural ecology, the bank vole provides insights into complex ecological interactions, evolutionary adaptations, and disease dynamics. Despite recent recognition of its importance in specific research areas, there is a lack of a comprehensive and up-to-date exploration of its role as a model organism. This review addresses this gap by offering a holistic examination of the bank vole's applications in ecology, evolution, biogeography, disease dynamics, and host-pathogen interactions. We emphasize novel insights into genetic variation, adaptation to climate change, population dynamics, experimental evolution, host-parasite co-evolution, and disease dynamics studies. By consolidating diverse research findings, this review provides a unique and comprehensive perspective on the bank vole's contributions to understanding ecology and evolution, underscoring its importance as a model organism in shaping future biological research.

• Klíčová slova
• Myodes glareolus, Bank vole, Ecology, Genetics, Model organism, Parasitology, Rodents,
• Publikační typ
• časopisecké články MeSH
• přehledy MeSH

Current species distributions at high latitudes are the product of expansion from glacial refugia into previously uninhabitable areas at the end of the last glaciation. The traditional view of postglacial colonization is that southern populations expanded their ranges into unoccupied northern territories. Recent findings on mitochondrial DNA (mtDNA) of British small mammals have challenged this simple colonization scenario by demonstrating a more complex genetic turnover in Britain during the Pleistocene-Holocene transition where one mtDNA clade of each species was replaced by another mtDNA clade of the same species. Here, we provide evidence from one of those small mammals, the bank vole (Clethrionomys glareolus), that the replacement was genome-wide. Using more than 10 000 autosomal SNPs we found that similar to mtDNA, bank vole genomes in Britain form two (north and south) clusters which admix. Therefore, the genome of the original postglacial colonists (the northern cluster) was probably replaced by another wave of migration from a different continental European population (the southern cluster), and we gained support for this by modelling with approximate Bayesian computation. This finding emphasizes the importance of analysis of genome-wide diversity within species under changing climate in creating opportunities for sophisticated testing of population history scenarios.

• Klíčová slova
• Clethrionomys glareolus, Myodes glareolus, approximate Bayesian computation, genome admixture, postglacial colonization, single-nucleotide polymorphism,
• MeSH
• Arvicolinae genetika   fyziologie   MeSH
• fylogeneze MeSH
• genom * MeSH
• jednonukleotidový polymorfismus * MeSH
• migrace zvířat * MeSH
• rozšíření zvířat * MeSH
• sekvenční analýza DNA MeSH
• zvířata MeSH
• Check Tag
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Geografické názvy
• Anglie MeSH
• Skotsko MeSH
• Wales MeSH

The major histocompatibility complex (MHC) plays a central role in the adaptive immune response and is the most polymorphic gene family in vertebrates. Although high-throughput sequencing has increasingly been used for genotyping families of co-amplifying MHC genes, its potential to facilitate early steps in the characterisation of MHC variation in nonmodel organism has not been fully explored. In this study we evaluated the usefulness of de novo transcriptome assembly in characterisation of MHC sequence diversity. We found that although de novo transcriptome assembly of MHC I genes does not reconstruct sequences of individual alleles, it does allow the identification of conserved regions for PCR primer design. Using the newly designed primers, we characterised MHC I sequences in the bank vole. Phylogenetic analysis of the partial MHC I coding sequence (2-4 exons) of the bank vole revealed a lack of orthology to MHC I of other Cricetidae, consistent with the high gene turnover of this region. The diversity of expressed alleles was characterised using ultra-deep sequencing of the third exon that codes for the peptide-binding region of the MHC molecule. High allelic diversity was demonstrated, with 72 alleles found in 29 individuals. Interindividual variation in the number of expressed loci was found, with the number of alleles per individual ranging from 5 to 14. Strong signatures of positive selection were found for 8 amino acid sites, most of which are inferred to bind antigens in human MHC, indicating conservation of structure despite rapid sequence evolution.

• MeSH
• alely MeSH
• Arvicolinae genetika   MeSH
• DNA primery MeSH
• exony MeSH
• fylogeneze MeSH
• genetická variace MeSH
• genotyp MeSH
• geny MHC třídy I * MeSH
• hlavní histokompatibilní komplex genetika   MeSH
• multigenová rodina MeSH
• myši MeSH
• transkriptom * MeSH
• vysoce účinné nukleotidové sekvenování MeSH
• zvířata MeSH
• Check Tag
• myši MeSH
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Názvy látek
• DNA primery MeSH

BACKGROUND: Although posttranscriptional modification of mitochondrial (mt) transcripts plays key roles in completion of the coding information and in the expression of mtDNA-encoded genes, there is little experimental evidence on the polyadenylation status and the location of mt gene poly(A) sites for non-human mammals. RESULTS: Poly(A)-enriched RNA-Seq reads collected for two wild-caught bank voles (Clethrionomys glareolus) were mapped to the complete mitochondrial genome of that species. Transcript polyadenylation was detected as unmapped adenine residues at the ends of the mapped reads. Where the tRNA punctuation model applied, there was the expected polyadenylation, except for the nad5 transcript, whose polyadenylated 3' end is at an intergenic sequence/cytochrome b boundary. As in human, two pairs of bank vole genes, nad4l/nad4 and atp8/atp6, are expressed from bicistronic transcripts. TAA stop codons of four bank vole protein-coding genes (nad1, atp6, cox3 and nad4) are incompletely encoded in the DNA and are completed by polyadenylation. This is three genes (nad2, nad3 and cob) less than in human. The bank vole nad2 gene encodes a full stop codon (TAA in one vole and TAG in the other), which is followed by a 2 bp UTR and the gene conforms to the tRNA punctuation model. In contrast, the annotations of the reference mouse and some other rodent mt genomes in GenBank include complete TAG stop codons in both nad1 and nad2, which overlap downstream trnI and trnW, respectively. Thus the RNA-Seq data of bank voles provides a model for stop codons of mt-encoded genes in mammals comparable to humans, but at odds with some of the interpretation based purely on genomic data in mouse and other rodents. CONCLUSIONS: This work demonstrates how RNA-Seq data were useful to recover mtDNA transcriptome data in a non-model rodent and to shed more light on mammalian mtDNA transcriptome and post-transcriptional modification. Even though gene content and organisation of mtDNA are strongly conserved among mammals, annotations that neglect the transcriptome may be prone to errors in relation to the stop codons.

• MeSH
• Arvicolinae genetika   MeSH
• genom mitochondriální genetika   MeSH
• mapování chromozomů MeSH
• mitochondriální DNA genetika   MeSH
• sekvenční analýza RNA MeSH
• zvířata MeSH
• Check Tag
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Názvy látek
• mitochondriální DNA MeSH

Over the years, researchers have used presumptively neutral molecular variation to infer the origins of current species' distributions in northern latitudes (especially Europe). However, several reported examples of genic and chromosomal replacements suggest that end-glacial colonizations of particular northern areas may have involved genetic input from different source populations at different times, coupled with competition and selection. We investigate the functional consequences of differences between two bank vole (Clethrionomys glareolus) haemoglobins deriving from different glacial refugia, one of which partially replaced the other in Britain during end-glacial climate warming. This allows us to examine their adaptive divergence and hence a possible role of selection in the replacement. We determine the amino acid substitution Ser52Cys in the major expressed β-globin gene as the allelic difference. We use structural modelling to reveal that the protein environment renders the 52Cys thiol a highly reactive functional group and we show its reactivity in vitro. We demonstrate that possessing the reactive thiol in haemoglobin increases the resistance of bank vole erythrocytes to oxidative stress. Our study thus provides striking evidence for physiological differences between products of genic variants that spread at the expense of one another during colonization of an area from different glacial refugia.

• Klíčová slova
• adaptation, antioxidative capacity, climate change, cysteine, oxidative stress, redox,
• MeSH
• Arvicolinae klasifikace   genetika   metabolismus   MeSH
• fylogeografie MeSH
• genetická variace MeSH
• hemoglobiny chemie   genetika   metabolismus   MeSH
• molekulární sekvence - údaje MeSH
• substituce aminokyselin MeSH
• zvířata MeSH
• Check Tag
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Geografické názvy
• Spojené království MeSH
• Názvy látek
• hemoglobiny MeSH