Search bioRxiv⌕ Search

Biology subjects

Pollet, N.

Publications and source records attributed to Pollet, N..

10 recordsLinked to original sources

Animal retrozymes are nonautonomous sequences of Penelope-like elements

Hammerhead ribozymes (HHRs) are small catalytic RNAs found across diverse life forms. In animal genomes, they can be encoded by genes organised in dispersed copies or in tandem genomic arrangements. These tandemly organised forms, known as Non-LTR retrozymes, were recently identified as a distinct group of non- autonomous retrotransposons, likely mobilised via a rolling-circle transposition mechanism and potentially involved in host transcriptome regulation. However, their evolutionary origins remain poorly understood. Here, we investigate the presence, genomic distribution, and possible origins of Non-LTR retrozymes across a broad range of vertebrate species. We find that these elements display a patchy phylogenetic distribution, notably absent from the Aves and Mammalia lineages. In species where they are present, retrozyme copy number, consensus length, and monomer proportion vary widely across species and retrozyme families, suggesting diverse amplification dynamics. Genomic mapping reveals a significant enrichment of Non-LTR retrozymes in intergenic regions and their exclusion from introns and exons, indicating selective pressure against genic insertion. Strikingly, the phylogenetic distribution of Non-LTR retrozymes coincides with that of Penelope-like elements (PLEs). Phylogenetic analysis further shows that the pLTR region of PLEs is closely related to Non-LTR retrozymes, supporting the hypothesis that Non-LTR retrozymes are non-autonomous derivatives of PLEs. Together, our findings shed new light on the evolutionary origin and genomic behaviour of Non-LTR retrozymes and underscore their potential regulatory roles in vertebrate genomes.

genomics↗

Microbial profiling of native and alien Drosophila in French Guiana reveals candidate taxa potentially affecting invasion dynamics.

Invasive alien species (IAS) represent a major threat to biodiversity, human health, and economy. Yet the role of host-associated microbiomes in invasion processes remains poorly understood in natural systems. Here, we investigated the bacterial and fungal microbiomes of IAS and native Drosophila species collected along an anthropization gradient in French Guiana. Analyses of Drosophila communities revealed that IAS establishment is limited outside coastal habitats. Using bacterial 16S rRNA and fungal ITS metabarcoding of pooled individuals, we assessed microbial diversity, composition, and structure across host species, host category (invasive vs. native), and locality. Bacterial communities associated with IAS harboured reduced alpha diversity and distinct community structure compared to native Drosophila species, and host phylogenetic relatedness and locality also contributed to bacteriome variation. In contrast, fungal communities were mainly structured by locality and host species. We further identified core and exclusive taxa, compared bacteriome composition between native and IAS hosts using global reference datasets, and integrated information from the microbiome literature. This approach led to the identification of 45 bacterial and fungal candidate taxa potentially associated with host adaptation or competitiveness across coastal and rainforest environments. Overall, our results highlight microbiome variation as a potential component of invasion dynamics in Neotropical Drosophila.

ecology↗

Ploidy-dependent modulation of DNA replication kinetics in Xenopus

DNA replication in multicellular organisms follows a tightly regulated spatio-temporal program. Although the mechanisms underlying this replication program remain only partially understood, studies in model systems such as Xenopus laevis have highlighted the importance of titrating low-abundance replication factors. Whole-genome duplications as a consequence of polyploidization introduce additional layers of complexity, yet comparative analyses of replication programs across closely related polyploid species are scarce. Here, we developed an interspecies in vitro replication system using X. laevis egg extracts and sperm nuclei from three Xenopus species with varying ploidy: diploid (X. tropicalis), tetraploid (X. laevis), and dodecaploid (X. eysoole). Replication in diploid X. tropicalis was faster than in tetraploid X. laevis nuclei, due to higher fork density and speed. Surprisingly, dodecaploid X. eysoole replication was also accelerated compared to tetraploid nuclei, suggesting that higher ploidy does not necessarily extend S phase. Since replication genes are highly conserved between these species, these results imply dynamic tuning of replication programs across polyploid species and shed light on the evolutionary adaptability of DNA replication in response to genome duplication.

molecular biology↗

Systematic annotation of Helitron-like elements in eukaryote genomes using HELIANO

Helitron-like elements (HLEs) are widespread eukaryotic DNA transposons employing a rolling-circle transposition mechanism. Despite their prevalence in fungi, animals, and plant genomes, identifying Helitrons remains challenging. We introduce HELIANO, a software for annotating and classifying autonomous and non-autonomous Helitron and Helentron sequences from whole genomes. HELIANO outperforms existing tools in speed and accuracy, demonstrated through benchmarking and its application to complex genomes (Xenopus tropicalis, Xenopus laevis, Oryza sativa), revealing numerous newly identified Helitrons and Helentrons. In a comprehensive analysis of 404 eukaryote genomes, we found HLEs widely distributed across phyla, with exceptions in specific taxa. Helentrons were identified in numerous land plant species, and 20 protein domains were discovered integrated within specific autonomous HLE families. A global phylogenetic analysis confirmed the classification into main clades Helentron and Helitron, revealing nine subgroups, some enriched in particular taxa. The future use of HELIANO will contribute to the global analysis of TEs across genomes and enhance our understanding of this transposon superfamily.

evolutionary biology↗

Maternal body condition affects the response of the gut microbiome to a widespread contaminant in larval spined toads

Glyphosates primary metabolite, aminomethylphosphonic acid (AMPA), is the most detected pollutant in surface waters. Recent studies have raised concerns about its toxicity, yet underlying mechanisms remain poorly understood. A disruption of the gut microbiome, which plays a crucial role in host health, could mediate most of the adverse effects. We investigated the impact of AMPA exposure on the gut microbiome of spined toad tadpoles (Bufo spinosus). We hypothesized that AMPA could alter the gut microbiota composition and that these effects could depend on the microbiota source. We exposed tadpoles to minute concentrations of AMPA and analyzed their faecal microbiota using 16S rRNA gene sequencing as a proxy of the gut microbiota. AMPA exposure decreased the gut bacterial biomass and affected the bacterial community composition of tadpoles faeces. Furthermore, we observed interactions between AMPA exposure and maternal body condition on the Bacteroidota and Actinobacteriota phyla abundances. This suggests a maternal effect on early-life microbial colonizers that could influence the response of the gut microbiome to AMPA. These findings highlight the importance of considering the gut microbiome when studying the effects of environmental contaminants. Further research is needed to elucidate the long-term implications of this microbiome alteration for amphibian health.

ecology↗

Analysis of a shark reveals ancient habenular asymmetries in gnathostomes and points to Wnt regulation as a driving force in their diversification

The origin of left-right asymmetries in the vertebrate habenula remains largely unknown. Using a transcriptomic approach, we show that in a cartilaginous fish, the catshark Scyliorhinus canicula, habenulae exhibit marked asymmetries both in their medial and their lateral component. Comparisons across gnathostomes suggest that asymmetries in the catshark lateral habenulae reflect an ancestral gnathostome trait, independently lost in tetrapods and neopterygians. Analysis of the mechanisms underlying their formation highlights an essential role of Wnt signaling. Wnt activity is submitted to a dynamic, asymmetric regulation during habenula development, with a Nodal dependent left repression at a stage when precursors for lateral habenulae have exited cell cycles. Pharmacological treatments during this time window reveal that Wnt signaling promotes lateral right neuronal identities in the right lateral habenula, while its repression by Nodal in the left one promotes lateral left neuronal identities. Based on comparisons with the zebrafish and the mouse, we propose that habenular asymmetry formation and diversification in gnathostomes involve the same developmental logic, relying on a conserved temporal regulation of neurogenesis, shaping neuronal identities on both sides, and its modification by a dynamic Wnt activity, right-restricted in the ancestral state and prone to variations in time and space during evolution.

developmental biology↗

The natural history of the black soldier fly, Hermetia illucens: insights from complete mitochondrial genome sequences

The Black Soldier Fly (BSF) Hermetia illucens is a cosmopolitan fly heavily used by industrial companies to reduce biowaste and produce protein and fat for poultry and aquaculture feed. However, the natural history and the genetic diversity of the BSF is poorly known. In this study, we analysed 677 CO1 sequences derived from samples found all over the five continents leading us to the discovery of 52 haplotypes including 10 major haplotypes. We refined the definition of these haplotypes by sequencing 59 mitochondrial genomes. We could derive an estimate of the separation events of the different haplotypes at more than two million years for the oldest branches. This worldwide cryptic genetic and genomic diversity is mirrored at local scale in France in which we found five major haplotypes sometimes in sympatry. Our data resolve the phylogenetic relationships between the major lineages and give insights into the dispersal and the numbers of BSF neo-introduction at global and local scales. Our results indicate that the genetic and genomic diversity of commercial BSF stock is very low and these brood stock participated in the dissemination of the BSF in the wild. Taken together these results call for a better understanding of the genomic diversity of the BSF to unravel possible specific adaptations of the different lineages for industrial needs and to initiate the selection process.

evolutionary biology↗

Insights on the evolution of vertebrate microbiomes from the analysis of the Xenopus frog microbiota across life stages

BackgroundThe microorganism world living in amphibians is still largely under-represented and under-studied in the literature. Among anuran amphibians, African clawed frogs of the Xenopus genus stand as well-characterized models with an in-depth knowledge of their developmental biological processes including their metamorphosis. In this study, we analyzed the succession of microbial communities and their activities across diverse body habitats of Xenopus tropicalis using different approaches including flow cytometry and 16s rDNA gene metabarcoding. We also evaluated the metabolic capacity of the premetamorphic tadpoles gut microbiome using metagenomic and metatranscriptomic sequencing. ResultsWe analyzed the bacterial components of the Xenopus gut microbiota, the adult gut biogeography, the succession of communities during ontogeny, the impact of the alimentation in shaping the tadpoles gut bacterial communities and the transmission of skin and fecal bacteria to the eggs. We also identified the most active gut bacteria and their metabolic contribution to tadpole physiology including carbohydrate breakdown, nitrogen recycling, essential amino-acids and vitamin biosynthesis. ConclusionsWe present a comprehensive new microbiome dataset of a laboratory amphibian model. Our data provide evidences that studies on the Xenopus tadpole model can shed light on the interactions between a vertebrate host and its microbiome. We interpret our findings in light of bile acids being key molecular components regulating the gut microbiome composition during amphibian development and metamorphosis. Further studies into the metabolic interactions between amphibian tadpoles and their microbiota during early development and metamorphosis should provide useful information on the evolution of host-microbiota interactions in vertebrates. This article has been peer-reviewed and recommended by Peer Community in Genomics https://doi.org/10.24072/pci.genomics.100005

genomics↗

A new method for long-read sequencing of animal mitochondrial genomes: application to the identification of equine mitochondrial DNA variants

BackgroundWe present here an approach to sequence whole mitochondrial genomes using nanopore long-read sequencing. Our method relies on the selective elimination of nuclear DNA using an exonuclease treatment and on the amplification of circular mitochondrial DNA using a multiple displacement amplification step. ResultsWe optimized each preparative step to obtain a 100 million-fold enrichment of horse mitochondrial DNA relative to nuclear DNA. We sequenced these amplified mitochondrial DNA using nanopore sequencing technology and obtained mitochondrial DNA reads that represented up to half of the sequencing output. The sequence reads were 2.3 kb of mean length and provided an even coverage of the mitochondrial genome. Long-reads spanning half or more of the whole mtDNA provided a coverage that varied between 118X and 488X. Finally, we identified SNPs with a precision of 98.1%; recall of 85.2% and a F1-score of 0.912. ConclusionsOur analyses show that our method to amplify mtDNA and to sequence it using the nanopore technology is usable for mitochondrial DNA variant analysis. With minor modifications, this approach could easily be applied to other large circular DNA molecules.

genomics↗

Characterizing Xenopus tropicalis endurance capacities with multilevel transcriptomics

Vertebrate endurance capacity is a phenotype with considerable genetic heterogeneity. RNA-Seq technologies are an ideal tool to investigate the involved genes and processes, but several challenges exist when the phenotype of interest has a complex genetic background. Difficulties manifest at the level of results interpretation because commonly used statistical methods are designed to identify strongly associated genes. If an observed phenotype can be achieved though multiple distinct genetic mechanisms then typical gene-centric methods come with the attached risk that signal may be lost or misconstrued.\n\nGene set analysis (GSA) methods are now widely accepted as a means to address some of the shortcomings of gene-by-gene analysis methods. We carry out both gene level and gene set level analyses on Xenopus tropicalis to identify the genetic factors that contribute to endurance heterogeneity. A typical workflow might consider gene level and pathway level analyses, but in this work we propose an additional focus at the intermediate level of functional modules. We generate functional modules for GSA testing in order to be explicit in how ontology information is used with respect to the functional genomics of Xenopus. Additionally, we make use of multiple assemblies to corroborate implicated genes and processes.\n\nWe identified 42 core genes, 10 functional modules, and 14 pathways based on gene expression differences between endurant and non-endurant frogs. The majority of the genes and processes are readily associated with muscle contraction or catabolism. A substantial number of these genes are involved in lipid metabolic processes, suggesting an important role in frog endurance heterogeneity. Unsurprisingly, many of the gene expression differences between endurant and non-endurant frogs can be distilled down to the capacity to utilize substrate for energy, but at the individual level frogs appear to make use of diverse machinery to achieve these differences.

bioinformatics↗