Evidence map›Paper›PMID 34465293›Full record

ArticleBMC genomics2021

The genome of the extremophile Artemia provides insight into strategies to cope with extreme environments.

Stephanie De Vos, Stephane Rombauts, Louis Coussement, Wannes Dermauw, Marnik Vuylsteke, Patrick Sorgeloos, James S Clegg, Ziro Nambu, Filip Van Nieuwerburgh, Parisa Norouzitallab and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 39 citations in OpenAlex.

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  9. A Na pump with reduced stoichiometry is up-regulated by brine shrimp in extreme salinities.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

15 authors at 3 institutions in 4 countries.

Stephanie De VosLaboratory of Aquaculture & Artemia Reference Center, Department of Animal Sciences and Aquatic Ecology, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.ORCID https://orcid.org/0000-0001-6830-6928
Stephane RombautsDepartment of Plant Systems Biology, VIB, Department of Biotechnology and Bioinformatics, Ghent University, Ghent, Belgium.ORCID https://orcid.org/0000-0002-3985-4981
Louis CoussementDepartment of Data Analysis and Mathematical Modelling, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.
Wannes DermauwDepartment of Plants and Crops, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.ORCID https://orcid.org/0000-0003-4612-8969
Marnik VuylstekeGNOMIXX, Boterbloemstraat 26, 9090, Melle, Belgium.
Patrick SorgeloosLaboratory of Aquaculture & Artemia Reference Center, Department of Animal Sciences and Aquatic Ecology, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.ORCID https://orcid.org/0000-0003-2435-8237
James S CleggCoastal and Marine Sciences Institute, University of California, Bodega Bay, Davis, CA, USA.
Ziro NambuDepartment of Medical Technology, School of Health Sciences, University of Occupational and Environmental Health, Japan, Kitakyushu, Fukuoka, Japan.
Filip Van NieuwerburghDepartment of Pharmaceutics, Faculty of Pharmaceutical Sciences, Ghent University, Ghent, Belgium.ORCID https://orcid.org/0000-0001-8815-5485
Parisa NorouzitallabLaboratory of Aquaculture & Artemia Reference Center, Department of Animal Sciences and Aquatic Ecology, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.ORCID https://orcid.org/0000-0002-1740-0444
Thomas Van LeeuwenDepartment of Plants and Crops, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.
Tim De MeyerDepartment of Data Analysis and Mathematical Modelling, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.ORCID https://orcid.org/0000-0003-2994-9693
Gilbert Van StappenLaboratory of Aquaculture & Artemia Reference Center, Department of Animal Sciences and Aquatic Ecology, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.ORCID https://orcid.org/0000-0002-6258-262X
Yves Van de PeerDepartment of Plant Systems Biology, VIB, Department of Biotechnology and Bioinformatics, Ghent University, Ghent, Belgium.ORCID https://orcid.org/0000-0003-4327-3730
Peter BossierLaboratory of Aquaculture & Artemia Reference Center, Department of Animal Sciences and Aquatic Ecology, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium. peter.bossier@ugent.be.ORCID https://orcid.org/0000-0002-6165-9111
Ghent University · BEBay Institute · USUniversity of Occupational and Environmental Health Japan · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBrine shrimp Artemia have an unequalled ability to endure extreme salinity and complete anoxia. This study aims to elucidate its strategies to cope with these stressors. RESULTS AND DISCUSSION: Here, we present the genome of an inbred A. franciscana Kellogg, 1906. We identified 21,828 genes of which, under high salinity, 674 genes and under anoxia, 900 genes were differentially expressed (42%, respectively 30% were annotated). Under high salinity, relevant stress genes and pathways included several Heat Shock Protein and Leaf Embryogenesis Abundant genes, as well as the trehalose metabolism. In addition, based on differential gene expression analysis, it can be hypothesized that a high oxidative stress response and endocytosis/exocytosis are potential salt management strategies, in addition to the expression of major facilitator superfamily genes responsible for transmembrane ion transport. Under anoxia, genes involved in mitochondrial function, mTOR signalling and autophagy were differentially expressed. Both high salt and anoxia enhanced degradation of erroneous proteins and protein chaperoning. Compared with other branchiopod genomes, Artemia had 0.03% contracted and 6% expanded orthogroups, in which 14% of the genes were differentially expressed under high salinity or anoxia. One phospholipase D gene family, shown to be important in plant stress response, was uniquely present in both extremophiles Artemia and the tardigrade Hypsibius dujardini, yet not differentially expressed under the described experimental conditions.

conclusionsA relatively complete genome of Artemia was assembled, annotated and analysed, facilitating research on its extremophile features, and providing a reference sequence for crustacean research.

Indexed as

ArtemiaExtremophilesAnimalsExtreme EnvironmentsHeat-Shock ProteinsSalinityHeat-Shock ProteinsAnnotationAnoxiaArtemiaArthropodAssemblyBrine shrimpExtremophileGenomeSalinityTranscriptome

Identifiers

PMID34465293
PMCPMC8406910
OpenAlexW3197570873

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.