Evidence map›Paper›PMID 38191669›Full record

ArticleNature cell biology2024

Selective gene expression maintains human tRNA anticodon pools during differentiation.

Lexi Gao, Andrew Behrens, Geraldine Rodschinka, Sergio Forcelloni, Sascha Wani, Katrin Strasser, Danny D Nedialkova

Open access · hybridAbstract read
In one paragraph

Article in Nature cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
15.7field-weighted citation impact, top 1% 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

50 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Review
  3. Translation fidelity mechanisms and their changes in aging.bioRxiv : the preprint server for biology · 2026
    Article
  4. Multilevel genomic constraints shape nuclear tRNA gene organization in plants.The Plant journal : for cell and molecular biology · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. The regulation, function and disease relevance of cytoplasmic tRNAs.Nature reviews. Molecular cell biology · 2026
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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

7 authors at 1 institution in 1 country.

Lexi Gao *Mechanisms of Protein Biogenesis, Max Planck Institute of Biochemistry, Martinsried, Germany.
Andrew Behrens *Mechanisms of Protein Biogenesis, Max Planck Institute of Biochemistry, Martinsried, Germany.
Geraldine RodschinkaMechanisms of Protein Biogenesis, Max Planck Institute of Biochemistry, Martinsried, Germany.
Sergio ForcelloniMechanisms of Protein Biogenesis, Max Planck Institute of Biochemistry, Martinsried, Germany.
Sascha WaniMechanisms of Protein Biogenesis, Max Planck Institute of Biochemistry, Martinsried, Germany.
Katrin StrasserMechanisms of Protein Biogenesis, Max Planck Institute of Biochemistry, Martinsried, Germany.
Danny D NedialkovaMechanisms of Protein Biogenesis, Max Planck Institute of Biochemistry, Martinsried, Germany. nedialkova@biochem.mpg.de.ORCID 0000-0001-8598-6021
Max Planck Institute of Biochemistry · DE

Funding

Wellcome Trust
6 · The paper itself

Abstract

Transfer RNAs are essential for translating genetic information into proteins. The human genome contains hundreds of predicted tRNA genes, many in multiple copies. How their expression is regulated to control tRNA repertoires is unknown. Here we combined quantitative tRNA profiling and chromatin immunoprecipitation with sequencing to measure tRNA expression following the differentiation of human induced pluripotent stem cells into neuronal and cardiac cells. We find that tRNA transcript levels vary substantially, whereas tRNA anticodon pools, which govern decoding rates, are more stable among cell types. Mechanistically, RNA polymerase III transcribes a wide range of tRNA genes in human induced pluripotent stem cells but on differentiation becomes constrained to a subset we define as housekeeping tRNAs. This shift is mediated by decreased mTORC1 signalling, which activates the RNA polymerase III repressor MAF1. Our data explain how tRNA anticodon pools are buffered to maintain decoding speed across cell types and reveal that mTORC1 drives selective tRNA expression during differentiation.

Indexed as

AnticodonInduced Pluripotent Stem CellsGene ExpressionHumansMechanistic Target of Rapamycin Complex 1RNA Polymerase IIIRNA, TransferAnticodonMechanistic Target of Rapamycin Complex 1RNA Polymerase IIIRNA, Transfer

Identifiers

PMID38191669
PMCPMC10791582
OpenAlexW4390663488

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.