Evidence map›Paper›PMID 35241478›Full record

ArticleGenes & development2022

NMD is required for timely cell fate transitions by fine-tuning gene expression and regulating translation.

Michelle Huth, Laura Santini, Elena Galimberti, Julia Ramesmayer, Fabian Titz-Teixeira, Robert Sehlke, Michael Oberhuemer, Sarah Stummer, Veronika Herzog, Marius Garmhausen and 14 more

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
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

30 citing papers in PubMed, 48 citations in OpenAlex.

  1. SRSF3 plays a key role in liver cancer sex disparity by facilitating hepatocyte expression of ERα and FOXA.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  9. Nonsense-mediated decay controls a negative feedback loop in innate immune sensing.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

24 authors at 6 institutions in 3 countries.

Michelle HuthMax Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.
Laura Santini *Max Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.
Elena Galimberti *Max Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.
Julia RamesmayerMax Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.
Fabian Titz-TeixeiraCluster of Excellence Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, 50931 Cologne, Germany.
Robert SehlkeCluster of Excellence Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, 50931 Cologne, Germany.
Michael OberhuemerMax Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.
Sarah StummerMax Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.
Veronika HerzogInstitute of Molecular Biotechnology, Vienna BioCenter, 1030 Vienna, Austria.
Marius GarmhausenCluster of Excellence Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, 50931 Cologne, Germany.
Merrit RomeikeMax Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.
Anastasia ChugunovaResearch Institute of Molecular Pathology, Vienna BioCenter, 1030 Vienna, Austria.
Friederike LeeschVienna BioCenter PhD Program, Doctoral School of the University of Vienna, Medical University of Vienna, 1030 Vienna, Austria.
Laurenz HolcikMax Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.ORCID 0000-0001-7855-3770
Klara WeipoltshammerDepartment for Cell and Developmental Biology, Medical University of Vienna, 1090 Vienna, Austria.
Andreas LacknerMax Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.
Christian SchoeferDepartment for Cell and Developmental Biology, Medical University of Vienna, 1090 Vienna, Austria.
Arndt von HaeselerMax Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.
Christa BueckerMax Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.
Andrea PauliResearch Institute of Molecular Pathology, Vienna BioCenter, 1030 Vienna, Austria.
Stefan L AmeresMax Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.
Austin SmithWellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 0AW, United Kingdom.
Andreas BeyerCluster of Excellence Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, 50931 Cologne, Germany.ORCID 0000-0002-3891-2123
Martin LeebMax Perutz Laboratories Vienna, University of Vienna, Vienna BioCenter, 1030 Vienna, Austria.ORCID 0000-0001-5114-4782
University of Vienna · ATUniversity of Cologne · DEResearch Institute of Molecular Pathology · ATInstitute of Molecular Biotechnology · ATMedical University of Vienna · ATWellcome/MRC Cambridge Stem Cell Institute · GB

Funding

Austrian Science Fund FWF DOC 72Austrian Science Fund FWF I 3786
6 · The paper itself

Abstract

Cell fate transitions depend on balanced rewiring of transcription and translation programs to mediate ordered developmental progression. Components of the nonsense-mediated mRNA decay (NMD) pathway have been implicated in regulating embryonic stem cell (ESC) differentiation, but the exact mechanism is unclear. Here we show that NMD controls expression levels of the translation initiation factor

Indexed as

Carrier ProteinsNonsense Mediated mRNA DecayGene ExpressionHeLa CellsHumansMechanistic Target of Rapamycin Complex 1Carrier ProteinsMechanistic Target of Rapamycin Complex 1SMG7 protein, humancell fate regulationembryonic stem cellsexit from naïve pluripotencynonsense-mediated mRNA decaypluripotencyRNA biologytranslation initiation

Identifiers

PMID35241478
PMCPMC8973849
OpenAlexW4214922868

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.