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Evolutionary histories of transposable elements in the genome of the largest living marsupial carnivore, the tasmanian devil
KTH, School of Biotechnology (BIO), Proteomics and Nanobiotechnology. KTH, Centres, Science for Life Laboratory, SciLifeLab. Senckenberg Gesellschaft für Naturforschung, Germany .
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2015 (English)In: Molecular biology and evolution, ISSN 0737-4038, E-ISSN 1537-1719, Vol. 32, no 5, 1268-1283 p.Article in journal (Refereed) Published
Abstract [en]

The largest living carnivorous marsupial, the Tasmanian devil (Sarcophilus harrisii), is the sole survivor of a lineage originating about 12 Ma. We set out to investigate the spectrum of transposable elements found in the Tasmanian devil genome, the first high-coverage genome of an Australian marsupial. Marsupial genomes have been shown to have the highest amount of transposable elements among vertebrates. We analyzed the horizontally transmitted DNA transposons OC1 and hAT-1-MEu in the Tasmanian devil genome. OC1 is present in all carnivorous marsupials, while having a very limited distribution among the remaining Australian marsupial orders. In contrast, hAT-1-MEu is present in all Australian marsupial orders, and has so far only been identified in a few placental mammals. We screened 158 introns for phylogenetically informative retrotransposons in the order Dasyuromorphia, and found that the youngest SINE (Short INterspersed Element), WSINE1, is no longer active in the subfamily Dasyuridae. The lack of detectable WSINE1 activity in this group may be due to a retrotransposon inactivation event approximately 30 Ma. We found that the Tasmanian devil genome contains a relatively low number of continuous full-length LINE-1 (Long INterspersed Element 1, L1) retrotransposons compared with the opossum genome. Furthermore, all L1 elements in the Tasmanian devil appeared to be nonfunctional. Hidden Markov Model approaches suggested that other potential sources of functional reverse transcriptase are absent from the genome. We discuss the issues associated with assembling long, highly similar L1 copies from short read Illumina data and describe how assembly artifacts can potentially lead to erroneous conclusions.

Place, publisher, year, edition, pages
2015. Vol. 32, no 5, 1268-1283 p.
Keyword [en]
DNA transposon, retrotransposon, Sarcophilus
National Category
Biochemistry and Molecular Biology Genetics
Identifiers
URN: urn:nbn:se:kth:diva-170291DOI: 10.1093/molbev/msv017ISI: 000355318400014PubMedID: 25633377Scopus ID: 2-s2.0-84929645896OAI: oai:DiVA.org:kth-170291DiVA: diva2:828836
Funder
Science for Life Laboratory - a national resource center for high-throughput molecular bioscience
Note

QC 20150630

Available from: 2015-06-30 Created: 2015-06-29 Last updated: 2017-12-04Bibliographically approved

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