Evidence map›Paper›PMID 30085210›Full record

ArticleNucleic acids research2018

The human Obg protein GTPBP10 is involved in mitoribosomal biogenesis.

Elena Lavdovskaia, Elisa Kolander, Emely Steube, Mandy Mong-Quyen Mai, Henning Urlaub, Ricarda Richter-Dennerlein

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Regulation of RNA-binding proteins by small biomolecules.Nature reviews. Molecular cell biology · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. A roadmap for ribosome assembly in human mitochondria.Nature structural & molecular biology · 2024
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. The RNA methyltransferase METTL8 installs mNature communications · 2022
    Article
  18. Review
  19. Developmentally regulated GTPases: structure, function and roles in disease.Cellular and molecular life sciences : CMLS · 2021
    Review
  20. Loss ofeLife · 2021
    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

6 authors at 2 institutions in 1 country.

Elena LavdovskaiaDepartment of Cellular Biochemistry, University Medical Center Göttingen, D-37073 Göttingen, Germany.
Elisa KolanderDepartment of Cellular Biochemistry, University Medical Center Göttingen, D-37073 Göttingen, Germany.
Emely SteubeDepartment of Cellular Biochemistry, University Medical Center Göttingen, D-37073 Göttingen, Germany.
Mandy Mong-Quyen MaiDepartment of Cellular Biochemistry, University Medical Center Göttingen, D-37073 Göttingen, Germany.
Henning UrlaubBioanalytical Mass Spectrometry Group, Max Planck Institute for Biophysical Chemistry, D-37077 Göttingen, Germany.
Ricarda Richter-DennerleinDepartment of Cellular Biochemistry, University Medical Center Göttingen, D-37073 Göttingen, Germany.
University of Göttingen · DEUniversitätsmedizin Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human mitochondrial translation apparatus, which synthesizes the core subunits of the oxidative phosphorylation system, is of central interest as mutations in several genes encoding for mitoribosomal proteins or translation factors cause severe human diseases. Little is known, how this complex machinery assembles from nuclear-encoded protein components and mitochondrial-encoded RNAs, and which ancillary factors are required to form a functional mitoribosome. We have characterized the human Obg protein GTPBP10, which associates specifically with the mitoribosomal large subunit at a late maturation state. Defining its interactome, we have shown that GTPBP10 is in a complex with other mtLSU biogenesis factors including mitochondrial RNA granule components, the 16S rRNA module and late mtLSU assembly factors such as MALSU1, SMCR7L, MTERF4 and NSUN4. GTPBP10 deficiency leads to a drastic reduction in 55S monosome formation resulting in defective mtDNA-expression and in a decrease in cell growth. Our results suggest that GTPBP10 is a ribosome biogenesis factor of the mtLSU required for late stages of maturation.

Indexed as

DNA, MitochondrialHumansMethyltransferasesMitochondriaMitochondrial ProteinsMitochondrial RibosomesMonomeric GTP-Binding ProteinsOxidative PhosphorylationRibosomal ProteinsRibosomesRNA, Ribosomal, 16STranscription FactorsDNA, MitochondrialGTPBP10 protein, humanMALSU1 protein, humanMethyltransferasesMitochondrial ProteinsMonomeric GTP-Binding ProteinsMTERF4 protein, humanNSUN4 protein, humanRibosomal ProteinsRNA, Ribosomal, 16STranscription Factors

Identifiers

PMID30085210
PMCPMC6144781
OpenAlexW2885054768

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.