Evidence map›Paper›PMID 30730892›Full record

ArticlePLoS genetics2019

A genetic variant associated with multiple sclerosis inversely affects the expression of CD58 and microRNA-548ac from the same gene.

Michael Hecker, Nina Boxberger, Nicole Illner, Brit Fitzner, Ina Schröder, Alexander Winkelmann, Ales Dudesek, Stefanie Meister, Dirk Koczan, Peter Lorenz and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. CD58 Immunobiology at a Glance.Frontiers in immunology · 2021
    Review
  9. Article
  10. Article
  11. Review
  12. BioMed research international · 2020
    Article
  13. An 11-bp Indel Polymorphism within theAnimals : an open access journal from MDPI · 2019
    Article
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

12 authors at 2 institutions in 1 country.

Michael HeckerUniversity of Rostock, Department of Neurology, Division of Neuroimmunology, Rostock, Germany.ORCID 0000-0001-7015-3094
Nina BoxbergerUniversity of Rostock, Department of Neurology, Division of Neuroimmunology, Rostock, Germany.
Nicole IllnerUniversity of Rostock, Department of Neurology, Division of Neuroimmunology, Rostock, Germany.
Brit FitznerUniversity of Rostock, Department of Neurology, Division of Neuroimmunology, Rostock, Germany.
Ina SchröderUniversity of Rostock, Department of Neurology, Division of Neuroimmunology, Rostock, Germany.
Alexander WinkelmannUniversity of Rostock, Department of Neurology, Division of Neuroimmunology, Rostock, Germany.
Ales DudesekUniversity of Rostock, Department of Neurology, Division of Neuroimmunology, Rostock, Germany.ORCID 0000-0002-5636-3965
Stefanie MeisterUniversity of Rostock, Department of Neurology, Division of Neuroimmunology, Rostock, Germany.
Dirk KoczanUniversity of Rostock, Institute of Immunology, Rostock, Germany.
Peter LorenzUniversity of Rostock, Institute of Immunology, Rostock, Germany.ORCID 0000-0001-7925-1002
Hans-Jürgen ThiesenSteinbeis Transfer Center for Proteome Analysis, Rostock, Germany.
Uwe Klaus ZettlUniversity of Rostock, Department of Neurology, Division of Neuroimmunology, Rostock, Germany.
University of Rostock · DESteinbeis Foundation · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome-wide association studies have identified more than 200 genetic variants to be associated with an increased risk of developing multiple sclerosis (MS). Still, little is known about the causal molecular mechanisms that underlie the genetic contribution to disease susceptibility. In this study, we investigated the role of the single-nucleotide polymorphism (SNP) rs1414273, which is located within the microRNA-548ac stem-loop sequence in the first intron of the CD58 gene. We conducted an expression quantitative trait locus (eQTL) analysis based on public RNA-sequencing and microarray data of blood-derived cells of more than 1000 subjects. Additionally, CD58 transcripts and mature hsa-miR-548ac molecules were measured using real-time PCR in peripheral blood samples of 32 MS patients. Cell culture experiments were performed to evaluate the efficiency of Drosha-mediated stem-loop processing dependent on genotype and to determine the target genes of this underexplored microRNA. Across different global populations and data sets, carriers of the MS risk allele showed reduced CD58 mRNA levels but increased hsa-miR-548ac levels. We provide evidence that the SNP rs1414273 might alter Drosha cleavage activity, thereby provoking partial uncoupling of CD58 gene expression and microRNA-548ac production from the shared primary transcript in immune cells. Moreover, the microRNA was found to regulate genes, which participate in inflammatory processes and in controlling the balance of protein folding and degradation. We thus uncovered new regulatory implications of the MS-associated haplotype of the CD58 gene locus, and we remind that paradoxical findings can be encountered in the analysis of eQTLs upon data aggregation. Our study illustrates that a better understanding of RNA processing events might help to establish the functional nature of genetic variants, which predispose to inflammatory and neurological diseases.

Indexed as

Polymorphism, Single NucleotideCD58 AntigensCohort StudiesComputer SimulationFemaleGenetic Association StudiesGenome-Wide Association StudyHeLa CellsHumansIntronsMaleMicroRNAsMiddle AgedModels, GeneticMultiple SclerosisNucleic Acid ConformationCD58 AntigensMicroRNAsMIRN548 microRNA, humanRNA, Messenger

Identifiers

PMID30730892
PMCPMC6382214
OpenAlexW2912427065

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.