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Historical RNA expression profiles from the extinct Tasmanian tiger
Stockholm University, Science for Life Laboratory (SciLifeLab). Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute. Centre for Palaeogenetics, Sweden.ORCID iD: 0000-0002-4393-1740
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute. Stockholm University, Science for Life Laboratory (SciLifeLab). UiT - The Arctic University of Norway, Norway.ORCID iD: 0000-0003-0352-3037
Stockholm University, Faculty of Humanities, Department of Archaeology and Classical Studies. Centre for Palaeogenetics, Sweden.ORCID iD: 0000-0001-7981-5795
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Number of Authors: 122023 (English)In: Genome Research, ISSN 1088-9051, E-ISSN 1549-5469, Vol. 33, no 8, p. 1299-1316Article in journal (Refereed) Published
Abstract [en]

Paleogenomics continues to yield valuable insights into the evolution, population dynamics, and ecology of our ancestors and other extinct species. However, DNA sequencing cannot reveal tissue-specific gene expression, cellular identity, or gene regulation, which are only attainable at the transcriptional level. Pioneering studies have shown that useful RNA can be extracted from ancient specimens preserved in permafrost and historical skins from extant canids, but no attempts have been made so far on extinct species. We extract, sequence, and analyze historical RNA from muscle and skin tissue of a ∼130-year-old Tasmanian tiger (Thylacinus cynocephalus) preserved in desiccation at room temperature in a museum collection. The transcriptional profiles closely resemble those of extant species, revealing specific anatomical features such as slow muscle fibers or blood infiltration. Metatranscriptomic analysis, RNA damage, tissue-specific RNA profiles, and expression hotspots genome-wide further confirm the thylacine origin of the sequences. RNA sequences are used to improve protein-coding and noncoding annotations, evidencing missing exonic loci and the location of ribosomal RNA genes while increasing the number of annotated thylacine microRNAs from 62 to 325. We discover a thylacine-specific microRNA isoform that could not have been confirmed without RNA evidence. Finally, we detect traces of RNA viruses, suggesting the possibility of profiling viral evolution. Our results represent the first successful attempt to obtain transcriptional profiles from an extinct animal species, providing thought-to-be-lost information on gene expression dynamics. These findings hold promising implications for the study of RNA molecules across the vast collections of natural history museums and from well-preserved permafrost remains.

Place, publisher, year, edition, pages
2023. Vol. 33, no 8, p. 1299-1316
National Category
Evolutionary Biology Genetics and Genomics
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URN: urn:nbn:se:su:diva-223963DOI: 10.1101/gr.277663.123ISI: 001090879900001PubMedID: 37463752Scopus ID: 2-s2.0-85173579499OAI: oai:DiVA.org:su-223963DiVA, id: diva2:1814450
Available from: 2023-11-24 Created: 2023-11-24 Last updated: 2025-02-01Bibliographically approved

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Mármol-Sánchez, EmilioFromm, BastianPochon, ZoéKalogeropoulos, PanagiotisEriksson, EliBiryukova, InnaSekar, VaishnoviDalén, LoveFriedländer, Marc R.

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Mármol-Sánchez, EmilioFromm, BastianOskolkov, NikolayPochon, ZoéKalogeropoulos, PanagiotisEriksson, EliBiryukova, InnaSekar, VaishnoviErsmark, ErikAndersson, BjörnDalén, LoveFriedländer, Marc R.
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Science for Life Laboratory (SciLifeLab)Department of Molecular Biosciences, The Wenner-Gren InstituteDepartment of Archaeology and Classical StudiesDepartment of Zoology
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