Evidence map›Paper›PMID 34983389›Full record

ArticleBMC genomics2022

Regulation of fatty acid desaturase- and immunity gene-expression by mbk-1/DYRK1A in Caenorhabditis elegans.

Hildegard I D Mack, Jennifer Kremer, Eva Albertini, Elisabeth K M Mack, Pidder Jansen-Dürr

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Loss ofbioRxiv : the preprint server for biology · 2026
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  4. ThemBio · 2024
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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

5 authors at 2 institutions in 2 countries.

Hildegard I D MackInstitute for Biomedical Aging Research, University of Innsbruck, Rennweg 10, 6020, Innsbruck, Austria. Hildegard.I.Mack@gmail.com.
Jennifer KremerDepartment of Hematology, Oncology and Immunology, Philipps-University Marburg, and University Hospital Giessen and Marburg, Baldingerstrasse, 35032, Marburg, Germany.
Eva AlbertiniInstitute for Biomedical Aging Research, University of Innsbruck, Rennweg 10, 6020, Innsbruck, Austria.
Elisabeth K M MackDepartment of Hematology, Oncology and Immunology, Philipps-University Marburg, and University Hospital Giessen and Marburg, Baldingerstrasse, 35032, Marburg, Germany.
Pidder Jansen-DürrInstitute for Biomedical Aging Research, University of Innsbruck, Rennweg 10, 6020, Innsbruck, Austria. pidder.jansen-duerr@uibk.ac.at.
Universität Innsbruck · ATUniversitätsklinikum Gießen und Marburg · DE

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
NIH HHS P40 OD010440
6 · The paper itself

Abstract

backgroundIn the nematode Caenorhabditis elegans, longevity in response to germline ablation, but not in response to reduced insulin/IGF1-like signaling, is strongly dependent on the conserved protein kinase minibrain-related kinase 1 (MBK-1). In humans, the MBK-1 ortholog DYRK1A is associated with a variety of disorders, most prominently with neurological defects observed in Down syndrome. To better understand mbk-1's physiological roles and their dependence on genetic background, we analyzed the influence of mbk-1 loss on the transcriptomes of wildtype and long-lived, germline-deficient or insulin-receptor defective, C. elegans strains by RNA-sequencing.

resultsmbk-1 loss elicited global changes in transcription that were less pronounced in insulin-receptor mutant than in germline-deficient or wildtype C. elegans. Irrespective of genetic background, mbk-1 regulated genes were enriched for functions in biological processes related to organic acid metabolism and pathogen defense. qPCR-studies confirmed mbk-1 dependent induction of all three C. elegans Δ9-fatty acid desaturases, fat-5, fat-6 and fat-7, in wildtype, germline-deficient and insulin-receptor mutant strains. Conversely, mbk-1 dependent expression patterns of selected pathogen resistance genes, including asp-12, dod-24 and drd-50, differed across the genetic backgrounds examined. Finally, cth-1 and cysl-2, two genes which connect pathogen resistance to the metabolism of the gaseous messenger and lifespan regulator hydrogen sulfide (H

conclusionOur work reveals previously unknown roles of C. elegans mbk-1 in the regulation of fatty acid desaturase- and H

Indexed as

Caenorhabditis elegansCaenorhabditis elegans ProteinsLongevityAnimalsFatty Acid DesaturasesGerm CellsProtein Serine-Threonine KinasesProtein-Tyrosine KinasesCaenorhabditis elegans ProteinsFatty Acid DesaturasesProtein Serine-Threonine KinasesProtein-Tyrosine KinasesAgingFatty acid desaturationGermline stem cellsHydrogen sulfideInsulin-like signalingLifespan regulationPathogen defenseRNA-seq

Identifiers

PMID34983389
PMCPMC8729107
OpenAlexW4205354356

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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.