Biology subjects

Puukko, T.

Publications and source records attributed to Puukko, T..

3 recordsLinked to original sources

bioRxiv2025

Genomic incompatibilities are persistent barriers when speciation happens with gene flow in Formica ants

A current goal of speciation research is to identify the loci underlying reproductive barriers between species. Locating such barrier loci in empirical data is difficult due to the often complex demographic history of diverged taxa and the heterogeneity in evolutionary forces across the genome. Here we take advantage of a natural case of hybridization between two wood ant species (Formica aquilonia and F. polyctena) to identify regions of reduced long-term gene flow using demographically explicit scans of non-admixed genomes. In addition we identify candidate Bateson-Dobzhansky-Muller incompatibilities (BDMIs) through an imbalanced recombinant haplotype frequency analysis of natural F. aquilonia x F. polyctena hybrid genomes. Both approaches find barriers that are scattered across the genome. Furthermore, candidate BDMIs significantly overlap with the long-term barriers identified by gIMble, indicating that incompatibilities have persisted despite divergence with gene flow between the wood ant species. Intriguingly, BDMIs interact in a network and the number of pairwise interactions a BDMI has correlates with its long-term barrier strength: hub-like BDMIs with many pairwise interactions reduce gene flow more effectively. Finally in regards to function, long-term barriers identified by gIMble arise outside regions of both gene coding sequences (CDS) and transposable elements. In contrast, regions where long-term barriers and BDMIs co-locate are significantly associated with introns, implying a potential role of alternative splicing or gene regulation in incompatibilities, rather than CDS divergence. Overall, our results highlight the underappreciated impact of multilocus BDMIs and the need to consider network connectivity of BDMIs in future work. SignificanceDetecting barrier loci that reduce gene flow between closely related species is a common goal of speciation research. However, reliable detection of barrier loci is difficult due to confounding signals in genomic data. Here we take advantage of two different, recently developed approaches and find that barrier loci between wood ant species are scattered across the genome, and despite on-going gene flow, maintain two distinct species. We reveal that genomic regions that are incompatible between the two species can act as persistent barriers, despite theoretical predictions for their collapse under gene flow. Connectivity between incompatibilities also seems to play an important role in barrier persistence. These results highlight the need to consider connectivity between barrier loci in future speciation research.

evolutionary biology↗

bioRxiv2024

Introgression and divergence in a young species group

The process of speciation concerns often not only pairs of species but rather groups of diverging and interacting taxa, as highlighted by recent research. Hence, to understand the evolution of species diversity and their persistence, it is crucial to understand how gene flow and evolution of reproductive isolation shape groups of closely related species. Using resequencing data, we disentangle here genomic patterns of divergence and introgression in five Formica rufa group wood ant species that are at the early stage of speciation. We first revise earlier mitochondrial phylogenies with a nuclear genomic tree, and demonstrate then introgression that is in line with observations of their current day natural hybridisation. Investigating the genome-wide differentiation and divergence we find correlations between population genetic parameters of divergence, differentiation, and diversity, that are in line with theoretical expectations for young species. Despite previously found evidence for polygenic species barriers, our data lacks the genome-wide correlation between differentiation and divergence that would be expected under a model of polygenic barriers. The likely explanation for this lack is the dominating effect of ancestral diversity at these early stages of speciation. As hybridisation has led to both deleterious and adaptive consequences within the group, we examined the signatures of introgression. We find no strong positive correlation between introgression and recombination, suggesting introgression does not have a predominantly deleterious effect. We also infer low diversity in the genomic regions with high proportions of introgression, consistent with the idea that selection has locally favoured introgression. This could be due to sharing of adaptive alleles or reduction of genetic load in the receiving species. Interestingly, gene flow in this group could potentially cross multiple species boundaries even in the absence of direct interbreeding between all the species. We discuss the long-term benefits and costs of introgression in young species, including the effect of environmental fluctuations and multi-species introgression.

evolutionary biology↗

bioRxiv2020

Genetic screen to saturate guard cell signaling network reveals a role of GDP-L-fucose metabolism in stomatal closure

Guard cells regulate plant gas exchange by controlling the aperture of stomatal pores. The process of stomatal closure involves a multi-input signaling network that governs the activity of ion channels, which in turn regulate guard cell turgor pressure and volume. Here we describe a forward genetic screen to identify novel components involved in stomatal movements. Through an ozone-sensitivity approach combined with whole-rosette gas exchange analysis, 130 mutants of established stomatal regulators and 76 novel mutants impaired in stomatal closure were identified. One of the novel mutants was mapped to MURUS1 (MUR1), the first enzyme in de novo GDP-L-fucose biosynthesis. Defects in synthesis or import of GDP-L-Fuc into the Golgi apparatus resulted in impaired stomatal closure to multiple stimuli. Stomatal phenotypes observed in mur1 were independent from the canonical guard cell signaling and instead could be related to altered mechanical properties of guard cell walls. Impaired fucosylation of xyloglucan, N-linked glycans and arabinogalactan proteins did not explain the aberrant function of mur1 stomata, however our data suggest that the stomatal phenotypes observed in mur1 can at least partially be attributed to defective dimerization of rhamnogalactouronan-II. In addition to providing the genetic framework for future studies on guard cell signaling, our work emphasizes the impact of fucose metabolism on stomatal movement.

plant biology↗