Evidence map›Paper›PMID 31340759›Full record

ArticleBMC genomics2019

Comparative transcriptomics suggest unique molecular adaptations within tardigrade lineages.

Maria Kamilari, Aslak Jørgensen, Morten Schiøtt, Nadja Møbjerg

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
18.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
  2. Review
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  5. Fibril Structure of Desiccation-Protective Tardigrade Protein CAHS-8.Angewandte Chemie (International ed. in English) · 2026
    Article
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  8. Biomolecular condensates-Prerequisites for anhydrobiosis?Protein science : a publication of the Protein Society · 2025
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Maria KamilariSection for Cell Biology and Physiology, Department of Biology, August Krogh Building, University of Copenhagen, Universitetsparken 13, Copenhagen, Denmark.
Aslak JørgensenSection for Cell Biology and Physiology, Department of Biology, August Krogh Building, University of Copenhagen, Universitetsparken 13, Copenhagen, Denmark.
Morten SchiøttSection for Ecology and Evolution, Department of Biology, University of Copenhagen, Universitetsparken 15, Copenhagen, Denmark.
Nadja MøbjergSection for Cell Biology and Physiology, Department of Biology, August Krogh Building, University of Copenhagen, Universitetsparken 13, Copenhagen, Denmark. nmobjerg@bio.ku.dk.ORCID http://orcid.org/0000-0002-5845-9047
University of Copenhagen · DK

Funding

H2020 Marie Skłodowska-Curie Actions () No 747087The Danish Council for Independent Research DFF-4090-00145Villum Fonden 17522
6 · The paper itself

Abstract

backgroundTardigrades are renowned for their ability to enter cryptobiosis (latent life) and endure extreme stress, including desiccation and freezing. Increased focus is on revealing molecular mechanisms underlying this tolerance. Here, we provide the first transcriptomes from the heterotardigrade Echiniscoides cf. sigismundi and the eutardigrade Richtersius cf. coronifer, and compare these with data from other tardigrades and six eukaryote models. Investigating 107 genes/gene families, our study provides a thorough analysis of tardigrade gene content with focus on stress tolerance.

resultsE. cf. sigismundi, a strong cryptobiont, apparently lacks expression of a number of stress related genes. Most conspicuous is the lack of transcripts from genes involved in classical Non-Homologous End Joining. Our analyses suggest that post-cryptobiotic survival in tardigrades could rely on high fidelity transcription-coupled DNA repair. Tardigrades seem to lack many peroxins, but they all have a comprehensive number of genes encoding proteins involved in antioxidant defense. The "tardigrade unique proteins" (CAHS, SAHS, MAHS, RvLEAM), seem to be missing in the heterotardigrade lineage, revealing that cryptobiosis in general cannot be attributed solely to these proteins. Our investigation further reveals a unique and highly expressed cold shock domain. We hypothesize that the cold shock protein acts as a RNA-chaperone involved in regulation of translation following freezing.

conclusionsOur results show common gene family contractions and expansions within stress related gene pathways in tardigrades, but also indicate that evolutionary lineages have a high degree of divergence. Different taxa and lineages may exhibit unique physiological adaptations towards stress conditions involving possible unknown functional homologues and/or novel physiological and biochemical mechanisms. To further substantiate the current results genome assemblies coupled with transcriptome data and experimental investigations are needed from tardigrades belonging to different evolutionary lineages.

Indexed as

TranscriptomeAnimalsBiological EvolutionDNA RepairMultigene FamilyRNA-SeqStress, PhysiologicalTardigradaCold shock domainFunctional gene categoriesModel organismsStress genesTardigradaTranscriptomics

Identifiers

PMID31340759
PMCPMC6652013
OpenAlexW2963886118

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.