Evidence map›Paper›PMID 31722427›Full record

ArticleNucleic acids research2019

Loss of the ribosomal RNA methyltransferase NSUN5 impairs global protein synthesis and normal growth.

Clemens Heissenberger, Lisa Liendl, Fabian Nagelreiter, Yulia Gonskikh, Guohuan Yang, Elena M Stelzer, Teresa L Krammer, Lucia Micutkova, Stefan Vogt, David P Kreil and 13 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% 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

82 citing papers in PubMed, 1 synthesis or guideline pooled it, 148 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Oxidative stress-driven mRedox biology · 2026
    Article
  7. Article
  8. Review
  9. NSUN5 and RNA mFrontiers in cell and developmental biology · 2026
    Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. NSUN5 promotes cholangiocarcinoma progression by enhancing GLS mRNA stabilization.Journal of cancer research and clinical oncology · 2025
    Article

22 more citing papers are in PubMed but not listed here.

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

23 authors at 6 institutions in 3 countries.

Clemens HeissenbergerDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Lisa LiendlDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Fabian NagelreiterDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Yulia GonskikhDepartment of Chemistry and Biochemistry, University of Bern, 3012 Bern, Switzerland.
Guohuan YangBiochemistry Center, University of Heidelberg, 69120 Heidelberg, Germany.
Elena M StelzerDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Teresa L KrammerDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Lucia MicutkovaInstitute for Biomedical Aging Research, University of Innsbruck, 6020 Innsbruck, Austria.
Stefan VogtDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
David P KreilDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Gerhard SekotDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Emilio SienaDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Ina PoserMax Planck Institute for Molecular Cell Biology and Genetics, 01307 Dresden, Germany.
Eva HarreitherDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Angela LinderDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Viktoria EhretDepartment of Biomedical Imaging and Image-guided Therapy, Division of Molecular and Gender Imaging, Preclinical Imaging Laboratory, Medical University of Vienna, 1090 Vienna, Austria.
Thomas H HelbichDepartment of Biomedical Imaging and Image-guided Therapy, Division of Molecular and Gender Imaging, Preclinical Imaging Laboratory, Medical University of Vienna, 1090 Vienna, Austria.
Regina Grillari-VoglauerDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Pidder Jansen-DürrInstitute for Biomedical Aging Research, University of Innsbruck, 6020 Innsbruck, Austria.
Martin KošBiochemistry Center, University of Heidelberg, 69120 Heidelberg, Germany.
Norbert PolacekDepartment of Chemistry and Biochemistry, University of Bern, 3012 Bern, Switzerland.
Johannes GrillariDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Markus SchossererDepartment of Biotechnology, Institute of Molecular Biotechnology, University of Natural Resources and Life Sciences, Vienna, 1190 Vienna, Austria.
Institute of Molecular Biotechnology · ATHeidelberg University · DEMedical University of Vienna · ATUniversität Innsbruck · ATUniversity of Bern · CHMax Planck Institute of Molecular Cell Biology and Genetics · DE

Funding

Austrian Science Fund FWF I 2514Austrian Science Fund FWF P 30623
6 · The paper itself

Abstract

Modifications of ribosomal RNA expand the nucleotide repertoire and thereby contribute to ribosome heterogeneity and translational regulation of gene expression. One particular m5C modification of 25S ribosomal RNA, which is introduced by Rcm1p, was previously shown to modulate stress responses and lifespan in yeast and other small organisms. Here, we report that NSUN5 is the functional orthologue of Rcm1p, introducing m5C3782 into human and m5C3438 into mouse 28S ribosomal RNA. Haploinsufficiency of the NSUN5 gene in fibroblasts from William Beuren syndrome patients causes partial loss of this modification. The N-terminal domain of NSUN5 is required for targeting to nucleoli, while two evolutionary highly conserved cysteines mediate catalysis. Phenotypic consequences of NSUN5 deficiency in mammalian cells include decreased proliferation and size, which can be attributed to a reduction in total protein synthesis by altered ribosomes. Strikingly, Nsun5 knockout in mice causes decreased body weight and lean mass without alterations in food intake, as well as a trend towards reduced protein synthesis in several tissues. Together, our findings emphasize the importance of single RNA modifications for ribosome function and normal cellular and organismal physiology.

Indexed as

AnimalsBody WeightCell EnlargementCell ProliferationCells, CulturedChildEmbryo, MammalianFemaleGene DeletionGrowth and DevelopmentHEK293 CellsHeLa CellsHumansInfantMaleMethyltransferasesMethyltransferasesMuscle ProteinsNSUN5 protein, human

Identifiers

PMID31722427
PMCPMC7145617
OpenAlexW2990525514

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.