25 research outputs found

    The changing influence of host genetics on the leaf fungal microbiome throughout plant development

    Get PDF
    Host genetics and the environment influence which fungal microbes colonize a plant. A new study in PLOS Biology finds that the relative influence of these factors changes throughout the development of the biofuel crop switchgrass growing in field settings

    Broad geographic sampling reveals the shared basis and environmental correlates of seasonal adaptation in Drosophila.

    Get PDF
    To advance our understanding of adaptation to temporally varying selection pressures, we identified signatures of seasonal adaptation occurring in parallel among Drosophila melanogaster populations. Specifically, we estimated allele frequencies genome-wide from flies sampled early and late in the growing season from 20 widely dispersed populations. We identified parallel seasonal allele frequency shifts across North America and Europe, demonstrating that seasonal adaptation is a general phenomenon of temperate fly populations. Seasonally fluctuating polymorphisms are enriched in large chromosomal inversions, and we find a broad concordance between seasonal and spatial allele frequency change. The direction of allele frequency change at seasonally variable polymorphisms can be predicted by weather conditions in the weeks prior to sampling, linking the environment and the genomic response to selection. Our results suggest that fluctuating selection is an important evolutionary force affecting patterns of genetic variation in Drosophila

    Genome-Wide Patterns of Adaptation to Temperate Environments Associated with Transposable Elements in Drosophila

    Get PDF
    Investigating spatial patterns of loci under selection can give insight into how populations evolved in response to selective pressures and can provide monitoring tools for detecting the impact of environmental changes on populations. Drosophila is a particularly good model to study adaptation to environmental heterogeneity since it is a tropical species that originated in sub-Saharan Africa and has only recently colonized the rest of the world. There is strong evidence for the adaptive role of Transposable Elements (TEs) in the evolution of Drosophila, and TEs might play an important role specifically in adaptation to temperate climates. In this work, we analyzed the frequency of a set of putatively adaptive and putatively neutral TEs in populations with contrasting climates that were collected near the endpoints of two known latitudinal clines in Australia and North America. The contrasting results obtained for putatively adaptive and putatively neutral TEs and the consistency of the patterns between continents strongly suggest that putatively adaptive TEs are involved in adaptation to temperate climates. We integrated information on population behavior, possible environmental selective agents, and both molecular and functional information of the TEs and their nearby genes to infer the plausible phenotypic consequences of these insertions. We conclude that adaptation to temperate environments is widespread in Drosophila and that TEs play a significant role in this adaptation. It is remarkable that such a diverse set of TEs located next to a diverse set of genes are consistently adaptive to temperate climate-related factors. We argue that reverse population genomic analyses, as the one described in this work, are necessary to arrive at a comprehensive picture of adaptation.[Author Summary] The potential of geographic studies of genetic variation for the understanding of adaptation has been recognized for some time. In Drosophila, most of the available studies are based on a priori candidates giving a biased picture of the genes and traits under spatially varying selection. In this work, we performed a genome-wide scan of adaptations to temperate climates associated with Transposable Element (TE) insertions. We integrated the available information of the identified TEs and their nearby genes to provide plausible hypotheses about the phenotypic consequences of these insertions. Considering the diversity of these TEs and the variety of genes into which they are inserted, it is surprising that their adaptive effects are consistently related to temperate climate-related factors. The TEs identified in this work add substantially to the markers available to monitor the impact of climate change on populations.This work was supported by grants from the National Institutes of Health (GM 077368) and the National Science Foundation (0317171) to DAP. PWM is a Human Frontier Science Program Postdoctoral Fellow.Peer reviewe

    What natural variation can teach us about resistance durability

    No full text
    Breeding a crop variety to be resistant to a pathogen usually takes years. This is problematic because pathogens, with short generation times and fluid genomes, adapt quickly to overcome resistance. The triumph of the pathogen is not inevitable, however, as there are numerous examples of durable resistance, particularly in wild plants. Which factors then contribute to such resistance stability over millennia? We review current knowledge of wild and agricultural pathosystems, detailing the importance of genetic, species and spatial heterogeneity in the prevention of pathogen outbreaks. We also highlight challenges associated with increasing resistance diversity in crops, both in light of pathogen (co-)evolution and breeding practices. Historically it has been difficult to incorporate heterogeneity into agriculture due to reduced efficiency in harvesting. Recent advances implementing computer vision and automation in agricultural production may improve our ability to harvest mixed genotype and mixed species plantings, thereby increasing resistance durability

    Differentiation between MAMP Triggered Defenses in <i>Arabidopsis thaliana</i>

    No full text
    <div><p>A first line of defense against pathogen attack for both plants and animals involves the detection of microbe-associated molecular patterns (MAMPs), followed by the induction of a complex immune response. Plants, like animals, encode several receptors that recognize different MAMPs. While these receptors are thought to function largely redundantly, the physiological responses to different MAMPs can differ in detail. Responses to MAMP exposure evolve quantitatively in natural populations of <i>Arabidopsis thaliana</i>, perhaps in response to environment specific differences in microbial threat. Here, we sought to determine the extent to which the detection of two canonical MAMPs were evolving redundantly or distinctly within natural populations. Our results reveal negligible correlation in plant growth responses between the bacterial MAMPs EF-Tu and flagellin. Further investigation of the genetic bases of differences in seedling growth inhibition and validation of 11 candidate genes reveal substantial differences in the genetic loci that underlie variation in response to these two MAMPs. Our results indicate that natural variation in MAMP recognition is largely MAMP-specific, indicating an ability to differentially tailor responses to EF-Tu and flagellin in <i>A. thaliana</i> populations.</p></div

    The maximum-likelihood phylogram of EFR protein coding sequence reveals two distinct haplotype groups.

    No full text
    <p>Phylogenetic analysis of 3,096 nucleotides of the <i>EFR</i> coding region of 109 <i>A. thaliana</i> genotypes that were also represented in the GWA mapping. The sequences were reconstructed from SNP data of the 1001 genome project (<a href="http://1001genomes.org/" target="_blank">http://1001genomes.org/</a>). All nodes are supported by 100 out of 100 bootstrap replicates. Vertical grey bars indicate two haplotype groups that exhibit 28 nucleotide differences. Genotype 8240 (i.e., Kulturen-1) is a strong outlier with 54 nucleotide differences compared to haplotype group 2.</p

    Manhattan plots of the GWA mapping for SGI induced by seven MAMP variants.

    No full text
    <p>The genome-wide distribution of the -log10 <i>p</i> -values of the SNP—phenotype associations are plotted as a function of the genomic position along the five chromosomes. The GWA study was conducted using EMMAX, which controls for population structure. The <i>x</i>-axis displays the position along the chromosome while the <i>y</i>-axis displays the <i>p</i>-value from a linear mixed model regression associating a given SNP with SGI. SNPs with minor allele frequency (MAF) < 0.05 were excluded. For clarity, only SNPs characterized by -log10(<i>p</i>-value) ≤ 1 are shown. The horizontal dashed line depicts the threshold for the 0.1% tail of the <i>p</i>-value distribution, which varies between peptide variants (flg22<sup><i>Pv</i></sup>: 0.00134 to elf18<sup><i>DC</i></sup>: 0.00088). SNPs that displayed above-threshold <i>p</i>-values were considered for further analysis. SNPs corresponding to rare alleles (0.05 > MAF > 0.1) are plotted in magenta. The right-most panel shows quantile plots of the expected versus observed <i>p</i>-values for each MAMP variant. Note the different scale of the y-axis of the uppermost panel. Genes that could be validated as underlying the natural variation in SGI are indicated in black. The <i>a priori</i> candidate genes <i>FLS2</i> and <i>BAK1</i> are not significantly associated with SGI but are indicated in gray for reference. A table with all genes underlying the different peak regions is available in the data folder of the repository bitbucket.org/mvetter/geneticbasissgi.</p
    corecore