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Sökning: WFRF:(Bornberg Bauer Erich) > (2015-2019)

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1.
  • Huang, Yun, et al. (författare)
  • Transcriptome profiling of immune tissues reveals habitat-specific gene expression between lake and river sticklebacks
  • 2016
  • Ingår i: Molecular Ecology. - : Wiley. - 0962-1083 .- 1365-294X. ; 25:4, s. 943-958
  • Tidskriftsartikel (refereegranskat)abstract
    • The observation of habitat-specific phenotypes suggests the action of natural selection. The three-spined stickleback (Gasterosteus aculeatus) has repeatedly colonized and adapted to diverse freshwater habitats across the northern hemisphere since the last glaciation, while giving rise to recurring phenotypes associated with specific habitats. Parapatric lake and river populations of sticklebacks harbour distinct parasite communities, a factor proposed to contribute to adaptive differentiation between these ecotypes. However, little is known about the transcriptional response to the distinct parasite pressure of those fish in a natural setting. Here, we sampled wild-caught sticklebacks across four geographical locations from lake and river habitats differing in their parasite load. We compared gene expression profiles between lake and river populations using 77 whole-transcriptome libraries from two immune-relevant tissues, the head kidney and the spleen. Differential expression analyses revealed 139 genes with habitat-specific expression patterns across the sampled population pairs. Among the 139 differentially expressed genes, eight are annotated with an immune function and 42 have been identified as differentially expressed in previous experimental studies in which fish have been immune challenged. Together, these findings reinforce the hypothesis that parasites contribute to adaptation of sticklebacks in lake and river habitats.
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2.
  • Kaduk, Mateusz, 1985- (författare)
  • Functional Inference from Orthology and Domain Architecture
  • 2018
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • Proteins are the basic building blocks of all living organisms. They play a central role in determining the structure of living beings and are required for essential chemical reactions. One of the main challenges in bioinformatics is to characterize the function of all proteins. The problem of understanding protein function can be approached by understanding their evolutionary history. Orthology analysis plays an important role in studying the evolutionary relation of proteins. Proteins are termed orthologs if they derive from a single gene in the species' last common ancestor, i.e. if they were separated by a speciation event. Orthologs are useful because they retain their function more often than other homologs. Inference of a complete set of orthologs for many species is computationally intensive. Currently, the fastest algorithms rely on graph-based approaches, which compare all-vs-all sequences and then cluster top hits into groups of orthologs. The initial step of performing all-vs-all comparisons is usually the primary computational challenge as it scales quadratically with the number of species. A new, more scalable and less computationally demanding method was developed to solve this problem without sacrificing accuracy. The Hieranoid 2 algorithm reduces computational complexity to almost linear by overcoming the necessity to perform all-vs-all similarity searches. The algorithm progresses along a known species tree, from leaves to root. Starting at the leaves, ortholog groups are predicted conventionally and then summarized at internal nodes to form pseudo-species. These pseudo-species are then re-used to search against other (pseudo-)species higher in the tree. This way the algorithm aggregates new ortholog groups hierarchically. The hierarchy is a natural structure to store and view large multi-species ortholog groups, and provides a complete picture of inferred evolutionary events. To facilitate explorative analysis of hierarchical groups of orthologs, a new online tool was created. The HieranoiDB website provides precomputed hierarchical groups of orthologs for a set of 66 species. It allows the user to search for orthology assignments using protein description, protein sequence, or species. Evolutionary events and meta information is added to the hierarchical groups of orthologs, which are shown graphically as interactive trees. This representation allows exploring, searching, and easier visual inspection of multi-species ortholog groups.The majority of orthology prediction methods focus on treating the whole protein sequence as a single evolutionary unit. However, proteins are often composed of individual units, called protein domains, that can have different evolutionary histories. To extend the full sequence based methodology to a domain-aware method, a new approach called Domainoid is proposed. Here, domains are extracted from full-length sequences and subjected to orthology inference. This allows Domainoid to find orthology that would be missed by a full sequence approach.Networks are a convenient graphical representation for showing a large number of functional associations between genes or proteins. They allow various analyses of graph properties, and can help visualize complex relationships. A framework for inferring comprehensive functional association networks was developed, called FunCoup. A major difference compared to other networks is FunCoup's extensive use of orthology relationships between species, which significantly boosts its coverage. Using naïve Bayesian classifiers to integrate 10 different evidence types and orthology transfer, FunCoup captures functional associations of many types, and provides comprehensive networks for 17 species across five gold-standards.
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3.
  • Olsen, Jeanine L, et al. (författare)
  • The genome of the seagrass Zostera marina reveals angiosperm adaptation to the sea.
  • 2016
  • Ingår i: Nature. - : Springer Science and Business Media LLC. - 1476-4687 .- 0028-0836. ; 530:7590, s. 331-5
  • Tidskriftsartikel (refereegranskat)abstract
    • Seagrasses colonized the sea on at least three independent occasions to form the basis of one of the most productive and widespread coastal ecosystems on the planet. Here we report the genome of Zostera marina (L.), the first, to our knowledge, marine angiosperm to be fully sequenced. This reveals unique insights into the genomic losses and gains involved in achieving the structural and physiological adaptations required for its marine lifestyle, arguably the most severe habitat shift ever accomplished by flowering plants. Key angiosperm innovations that were lost include the entire repertoire of stomatal genes, genes involved in the synthesis of terpenoids and ethylene signalling, and genes for ultraviolet protection and phytochromes for far-red sensing. Seagrasses have also regained functions enabling them to adjust to full salinity. Their cell walls contain all of the polysaccharides typical of land plants, but also contain polyanionic, low-methylated pectins and sulfated galactans, a feature shared with the cell walls of all macroalgae and that is important for ion homoeostasis, nutrient uptake and O2/CO2 exchange through leaf epidermal cells. The Z. marina genome resource will markedly advance a wide range of functional ecological studies from adaptation of marine ecosystems under climate warming, to unravelling the mechanisms of osmoregulation under high salinities that may further inform our understanding of the evolution of salt tolerance in crop plants.
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4.
  • Yang, Gloria, et al. (författare)
  • Higher-order epistasis shapes the fitness landscape of a xenobiotic-degrading enzyme
  • 2019
  • Ingår i: Nature Chemical Biology. - : NATURE PUBLISHING GROUP. - 1552-4450 .- 1552-4469. ; 15:11, s. 1120-1128
  • Tidskriftsartikel (refereegranskat)abstract
    • Characterizing the adaptive landscapes that encompass the emergence of novel enzyme functions can provide molecular insights into both enzymatic and evolutionary mechanisms. Here, we combine ancestral protein reconstruction with biochemical, structural and mutational analyses to characterize the functional evolution of methyl-parathion hydrolase (MPH), an organophosphate-degrading enzyme. We identify five mutations that are necessary and sufficient for the evolution of MPH from an ancestral dihydrocoumarin hydrolase. In-depth analyses of the adaptive landscapes encompassing this evolutionary transition revealed that the mutations form a complex interaction network, defined in part by higher-order epistasis, that constrained the adaptive pathways available. By also characterizing the adaptive landscapes in terms of their functional activities towards three additional organophosphate substrates, we reveal that subtle differences in the polarity of the substrate substituents drastically alter the network of epistatic interactions. Our work suggests that the mutations function collectively to enable substrate recognition via subtle structural repositioning.
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