Table_1_Genomic and Transcriptomic Differentiation of Independent Invasions of the Pacific Oyster Crassostrea gigas.xlsx

• Main Authors: K. Mathias Wegner, Ana Lokmer, Uwe John
• Format: Dataset
• Language: unknown
• Published: 2020
• Subjects: Evolutionary Biology; Ecology; Invasive Species Ecology; Landscape Ecology; Conservation and Biodiversity; Behavioural Ecology; Community Ecology (excl. Invasive Species Ecology); Ecological Physiology; Freshwater Ecology; Marine and Estuarine Ecology (incl. Marine Ichthyology); Population Ecology; Terrestrial Ecology; biological invasion; genomics; genetic differentiation; FST outlier; adaptation; gene expression; Pacific; Crassostrea gigas; Pacific oyster
• Online Access: https://doi.org/10.3389/fevo.2020.567049.s001; https://figshare.com/articles/dataset/Table_1_Genomic_and_Transcriptomic_Differentiation_of_Independent_Invasions_of_the_Pacific_Oyster_Crassostrea_gigas_xlsx/13141256

Upon colonizing new habitats, invasive species face a series of new selection pressures as a result of changing abiotic conditions and novel biotic interactions with native species. These new selection pressures can be accommodated by different mechanisms that act on different levels and across different time scales: (1) By changing transcriptomic profiles, species can react by plasticity within individual physiological limitations. (2) Invasive populations can adapt by fixing beneficial genetic variants in response to the newly encountered selection pressures. Here, we compare the genomic and transcriptomic landscapes of two independent invasions of the Pacific Oyster (Crassostrea gigas) into the North Sea. In detail, we combine ddRAD sequencing on the genomic level with RNAseq on the transcriptomic level to reveal outlier loci (SNPs) indicative of adaptation, as well as transcriptomic profiles from a translocation experiment to show immediate physiological reactions between two populations characterizing the two independent invasions. Generally, we found low physical congruence between differentially regulated genes and outlier loci, indicating that different genes are involved on the different time scales. Functionally matching outlier loci and differentially expressed genes were however found for spliceosomal modification of mRNA and particularly for transposon activation, indicating that these variation creating processes might be connected across eco-physiological and evolutionary time scales. By contrasting and identifying functional congruence between population outlier loci and population specific transcriptomic profiles, we can thus reveal a glimpse at the traits and processes characterizing specific mechanisms involved in successful invasions.