23
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Genomic Takeover by Transposable Elements in the Strawberry Poison Frog

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          We sequenced the genome of the strawberry poison frog, Oophaga pumilio, at a depth of 127.5× using variable insert size libraries. The total genome size is estimated to be 6.76 Gb, of which 4.76 Gb are from high copy number repetitive elements with low differentiation across copies. These repeats encompass DNA transposons, RNA transposons, and LTR retrotransposons, including at least 0.4 and 1.0 Gb of Mariner/Tc1 and Gypsy elements, respectively. Expression data indicate high levels of gypsy and Mariner/ Tc1 expression in ova of O. pumilio compared with Xenopus laevis. We further observe phylogenetic evidence for horizontal transfer (HT) of Mariner elements, possibly between fish and frogs. The elements affected by HT are present in high copy number and are highly expressed, suggesting ongoing proliferation after HT. Our results suggest that the large amphibian genome sizes, at least partially, can be explained by a process of repeated invasion of new transposable elements that are not yet suppressed in the germline. We also find changes in the spliceosome that we hypothesize are related to permissiveness of O. pumilio to increases in intron length due to transposon proliferation. Finally, we identify the complement of ion channels in the first genomic sequenced poison frog and discuss its relation to the evolution of autoresistance to toxins sequestered in the skin.

          Related collections

          Most cited references56

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          Gene prediction in eukaryotes with a generalized hidden Markov model that uses hints from external sources

          Background In order to improve gene prediction, extrinsic evidence on the gene structure can be collected from various sources of information such as genome-genome comparisons and EST and protein alignments. However, such evidence is often incomplete and usually uncertain. The extrinsic evidence is usually not sufficient to recover the complete gene structure of all genes completely and the available evidence is often unreliable. Therefore extrinsic evidence is most valuable when it is balanced with sequence-intrinsic evidence. Results We present a fairly general method for integration of external information. Our method is based on the evaluation of hints to potentially protein-coding regions by means of a Generalized Hidden Markov Model (GHMM) that takes both intrinsic and extrinsic information into account. We used this method to extend the ab initio gene prediction program AUGUSTUS to a versatile tool that we call AUGUSTUS+. In this study, we focus on hints derived from matches to an EST or protein database, but our approach can be used to include arbitrary user-defined hints. Our method is only moderately effected by the length of a database match. Further, it exploits the information that can be derived from the absence of such matches. As a special case, AUGUSTUS+ can predict genes under user-defined constraints, e.g. if the positions of certain exons are known. With hints from EST and protein databases, our new approach was able to predict 89% of the exons in human chromosome 22 correctly. Conclusion Sensitive probabilistic modeling of extrinsic evidence such as sequence database matches can increase gene prediction accuracy. When a match of a sequence interval to an EST or protein sequence is used it should be treated as compound information rather than as information about individual positions.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            The impact of transposable elements in environmental adaptation.

            Transposable elements (TEs) play an important role in the responsive capacity of their hosts in the face of environmental challenges. The variety of mechanisms by which TEs influence the capacity of adaptation of the host is as large as the variety of TEs and host genomes. For example, TEs might directly affect the function of individual genes, provide a mechanism for rapidly acquiring new genetic material and disseminate regulatory elements that can lead to the creation of stress-inducible regulatory networks. In this review, we summarize recent examples that are part of an increasing body of evidence suggesting a significant role of TEs in the host response to an ever-changing environment, both in prokaryote and in eukaryote organisms. We argue that in the near future, the increasing availability of genome sequences and the development of new tools to discover and analyse TE insertions will further show the relevant role of TEs in environmental adaptation. © 2013 Blackwell Publishing Ltd.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              The contributions of transposable elements to the structure, function, and evolution of plant genomes.

              Transposable elements (TEs) are the key players in generating genomic novelty by a combination of the chromosome rearrangements they cause and the genes that come under their regulatory sway. Genome size, gene content, gene order, centromere function, and numerous other aspects of nuclear biology are driven by TE activity. Although the origins and attitudes of TEs have the hallmarks of selfish DNA, there are numerous cases where TE components have been co-opted by the host to create new genes or modify gene regulation. In particular, epigenetic regulation has been transformed from a process to silence invading TEs and viruses into a key strategy for regulating plant genes. Most, perhaps all, of this epigenetic regulation is derived from TE insertions near genes or TE-encoded factors that act in trans. Enormous pools of genome data and new technologies for reverse genetics will lead to a powerful new era of TE analysis in plants.
                Bookmark

                Author and article information

                Contributors
                Role: Associate Editor
                Journal
                Mol Biol Evol
                Mol. Biol. Evol
                molbev
                Molecular Biology and Evolution
                Oxford University Press
                0737-4038
                1537-1719
                December 2018
                25 September 2018
                25 September 2018
                : 35
                : 12
                : 2913-2927
                Affiliations
                [1 ]Department of Bioinformatics and Genomics, University of North Carolina at Charlotte, Charlotte, NC
                [2 ]State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, China
                [3 ]China National Genebank, BGI-Shenzhen, Shenzhen, Guangdong, China
                [4 ]Harvard Medical School, Harvard University, Cambridge, MA
                [5 ]Department of Ecology and Evolution, University of Chicago, Chicago, IL
                [6 ]Department of Integrative Biology, University of California, Berkeley, Berkeley, CA
                [7 ]Department of Biological Sciences, University of Pittsburgh, Pittsburgh, PA
                [8 ]Department of Molecular Cellular and Biomedical Sciences, University of New Hampshire, Durham, NH
                [9 ]Hubbard Center for Genomic Studies, University of New Hampshire, Durham, NH
                [10 ]Department of Biology, Eastern Carolina University, Greenville, NC
                [11 ]Department of Computer Science, University of Connecticut, Storrs, CT
                [12 ]James D. Watson Institute of Genome Sciences, Hangzhou, China
                [13 ]Department of Biology, Centre for Social Evolution, Universitetsparken 15, University of Copenhagen, Copenhagen, Denmark
                Author notes

                These authors are co-first authors.

                [‡]

                These authors are co-corresponding authors.

                Corresponding author: E-mail: rasmus_nielsen@ 123456berkeley.edu
                Author information
                http://orcid.org/0000-0002-2368-6960
                Article
                msy185
                10.1093/molbev/msy185
                6278860
                30517748
                8538c60e-14b1-4039-9394-037dac5ceb9d
                © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                Page count
                Pages: 15
                Funding
                Funded by: National Science Foundation 10.13039/100000001
                Award ID: 0701165
                Award ID: 1146370
                Funded by: NSF 10.13039/100000001
                Award ID: DEB 1655336
                Categories
                Discoveries

                Molecular biology
                transposable elements,amphibian genomics,poison frogs,horizontal transfer
                Molecular biology
                transposable elements, amphibian genomics, poison frogs, horizontal transfer

                Comments

                Comment on this article