Evidence map›Paper›PMID 24448271›Full record

ArticleRNA biology2013

Diversity of human tRNA genes from the 1000-genomes project.

Marc Parisien, Xiaoyun Wang, Tao Pan

Open access · hybridAbstract read
In one paragraph

Article in RNA biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

75 citing papers in PubMed, 103 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Natural human tRNARNA (New York, N.Y.) · 2025
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Missense suppressor tRNA therapeutics correct disease-causing alleles by misreading the genetic code.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  18. Engineered mischarged transfer RNAs for correcting pathogenic missense mutations.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  19. Article
  20. Article

15 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

3 authors at 1 institution in 1 country.

Marc ParisienDepartment of Biochemistry and Molecular Biology; University of Chicago; Chicago, IL USA Keywords: tRNA, isodecoder, SNP, 1000 genomes project.
Xiaoyun WangDepartment of Biochemistry and Molecular Biology; University of Chicago; Chicago, IL USA Keywords: tRNA, isodecoder, SNP, 1000 genomes project.
Tao PanDepartment of Biochemistry and Molecular Biology; University of Chicago; Chicago, IL USA Keywords: tRNA, isodecoder, SNP, 1000 genomes project.
University of Chicago · US

Funding

Mis-translation as a new mechanism of stress response in biologyDP1GM105386 · NIGMS · UNIVERSITY OF CHICAGO · PI PAN, TAO · 2012 to 2015
$3.1M
NCCDPHP CDC HHS DP1GM105386NIGMS NIH HHS DP1 GM105386
6 · The paper itself

Abstract

The sequence diversity of individual human genomes has been extensively analyzed for variations and phenotypic implications for mRNA, miRNA, and long non-coding RNA genes. TRNA (tRNA) also exhibits large sequence diversity in the human genome, but tRNA gene sequence variation and potential functional implications in individual human genomes have not been investigated. Here we capitalize on the sequencing data from the 1000-genomes project to examine the diversity of tRNA genes in the human population. Previous analysis of the reference human genome indicated an unexpected large number of diverse tRNA genes beyond the necessity of translation, suggesting that some tRNA transcripts may perform non-canonical functions. We found 24 new tRNA sequences in>1% and 76 new tRNA sequences in>0.2% of all individuals, indicating that tRNA genes are also subject to evolutionary changes in the human population. Unexpectedly, two abundant new tRNA genes contain base-pair mismatches in the anticodon stem. We experimentally determined that these two new tRNAs have altered structures in vitro; however, one new tRNA is not aminoacylated but extremely stable in HeLa cells, suggesting that this new tRNA can be used for non-canonical function. Our results show that at the scale of human population, tRNA genes are more diverse than conventionally understood, and some new tRNAs may perform non-canonical, extra-translational functions that may be linked to human health and disease.

Indexed as

Genome, HumanAnticodonBase Pair MismatchEvolution, MolecularGenetic VariationHeLa CellsHumansPhylogenyRNA, TransferTransfer RNA AminoacylationAnticodonRNA, Transfer1000 genomes projectisodecoderSNPtRNA

Identifiers

PMID24448271
PMCPMC3917988
OpenAlexW2001394720

What OpenQuestion holds

Textmetadata
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.