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Kreyling, J.

Publications and source records attributed to Kreyling, J..

3 recordsLinked to original sources

How drought and ploidy level shape gene expression and DNA methylation in Phragmites australis

Drought stress significantly affects plant physiology and growth, yet the molecular mechanisms underlying drought responses remain poorly understood. In this study, we investigate how tetraploid and octoploid Phragmites australis (common reed), a key species in wetland ecosystems and paludiculture, respond to drought at the transcriptional and epigenetic levels. Using RNA-seq, we identify changes in gene expression after 20 and 30 days of drought and assess methylation-sensitive amplification polymorphism (MSAP) over 50 days of drought. Transcriptomic analysis reveals that key drought-response genes are shared between ploidy levels, including those involved in the saccharopine pathway, water deprivation response, cell wall remodelling, and the mevalonate pathway. Drought supresses photosynthesis, with a pronounced down-regulation of the photosynthetic gene PsbP. Ploidy level influences gene expression under both drought and non-stress conditions, highlighting distinct adaptive strategies. In control samples, gene expression differed between ploidy levels, with octoploids up-regulating genes related to translation and metabolism, while tetraploids activate genes involved in cell wall modification and transmembrane transport. Prolonged drought increases DNA methylation variability, though no significant correlation is found between methylation levels and drought duration. Methylation differences are more pronounced between ploidy levels, with octoploids exhibiting lower overall methylation. These findings highlight the complex interactions between gene expression, epigenetic modifications, and polyploidy in drought response and provide a theoretical framework for future selection, hybridization, and conservation initiatives. Main ConclusionKey drought-response genes regulate saccharopine and mevalonate pathways, and cell wall remodelling. Ploidy level influences gene expression under drought and non-stress conditions. Octoploids overall exhibit lower methylation than tetraploids.

ecology↗

Higher ploidy coincides with inferior performance and no difference in stress tolerance in reed

(1) Climate change leads to more extreme weather events. Therefore, a high stress tolerance is becoming more critical for plants, with higher ploidy being reported to lead to higher stress tolerance. Phragmites australis (P. australis) is a target species for paludiculture, i.e. the wet use of peatlands, and well known for its many ploidy levels. (2) We expected octoploid genotypes of P. australis to outperform tetraploid ones in a 15-month mesocosm experiment including a gradient of 0 to 100 days of drought. We used pairs of genotypes differing in ploidy from three different geographic regions. (3) Increasing drought length led to a decrease in growth, biomass, morphological and ecophysiological traits in both ploidy levels, but 4x outperformed 8x in almost all traits under constant water supply (e.g., 2.5-fold more biomass production) and up to moderate drought (about 50 days). Under severe and prolonged drought, both ploidy levels performed equally poorly. (4) Our study suggests that higher ploidy levels do not necessarily outperform lower ploidy levels of P. australis under stressful conditions. In this species, ploidy alone may not explain performance, but the genotype can be as or more important than ploidy.

ecology↗

Rapid ecological and evolutionary divergence during a poleward range expansion

In response to climate change, a northward range expansion has been observed in many species. The wasp spider, Argiope bruennichi, has expanded from its historic range in the Mediterranean ("core"), now reaching as far as the Baltic States and Scandinavia ("edge"), even faster than the pace of climate change. We explored life history traits, adult phenotypes, offspring cold tolerance, and genomic patterns across the European range of A. bruennichi, and found origin-, environment- and life stage-specific responses to the cold northern climate. Wasp spiders have shifted their phenology at the edge, with females maturing earlier and at a smaller size, but maintaining similar pigmentation, clutch sizes, and hatching success compared to the core region. Using a reciprocal common garden experiment on overwintering offspring from the core and edge, we found evidence for genetic adaptation and considerable phenotypic plasticity. Overwintering survival was lower under the cold winter treatment for spiderlings from both origins. However, the edge-origin spiderlings that survived the winter had lower lethal temperatures and enhanced supercooling ability with reduced phenotypic plasticity in supercooling points compared to core spiderlings, while the chill coma recovery time was similar. Metabolomic analysis revealed accumulations of amino acids and myo-inositol in the cold winter treatment, particularly in spiderlings from the edge population, suggesting a role of these metabolites in improving cold tolerance. Genotype-environment tests showed strong genetic association across the genome to seasonality and minimum winter temperature. The population genomic analysis across the European range splits A. bruennichi into two distinct genetic clusters through the center of Germany, which roughly aligns with turnover from an oceanic to continental climate zone, complementing the genotype-environment test results. Overall, our study highlights the importance of integrating data on phenological shifts, changes in life-history, and life stage-specific phenotypic plasticity and genetic adaptation to understand the impacts of range expansions and shifts. The nuanced processes of acclimation and adaptation we uncovered advocate for holistic investigations of evolutionary fitness and fitness-related traits in the context of organismal responses to novel and changing environments.

ecology↗