Evidence map›Paper›PMID 24452241›Full record

ArticleRNA biology2014

RPL39L is an example of a recently evolved ribosomal protein paralog that shows highly specific tissue expression patterns and is upregulated in ESCs and HCC tumors.

Queenie Wing-Lei Wong, Jia Li, Sheng Rong Ng, Seng Gee Lim, Henry Yang, Leah A Vardy

Open access · hybridAbstract read
In one paragraph

Article in RNA biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

42 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Article
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  4. Ribosomal protein paralogues in ribosome specialization.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  5. Specialized ribosomes: integrating new insights and current challenges.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  6. Built differently or defective: can RNA exosomopathies cause ribosome heterogeneity?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  7. Article
  8. Review
  9. Article
  10. High-resolution reconstruction of aRNA (New York, N.Y.) · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Specialized Ribosomes in Health and Disease.International journal of molecular sciences · 2023
    Review
  18. Article
  19. Review
  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

6 authors at 5 institutions in 1 country.

Queenie Wing-Lei WongA*STAR Institute of Medical Biology; 8A Biomedical Grove; Immunos, Singapore.
Jia LiCancer Science Institute; National University of Singapore; Singapore.
Sheng Rong NgA*STAR Institute of Medical Biology; 8A Biomedical Grove; Immunos, Singapore.
Seng Gee LimDepartment of Medicine; Yong Loo Lin School of Medicine; National University of Singapore; Singapore.
Henry YangCancer Science Institute; National University of Singapore; Singapore.
Leah A VardyA*STAR Institute of Medical Biology; 8A Biomedical Grove; Immunos, Singapore; School of Biological Sciences; Nanyang Technological University; Singapore.
National University of Singapore · SGAgency for Science, Technology and Research · SGInstitute of Medical Biology · SGNational University Cancer Institute, Singapore · SGSingapore Immunology Network · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ribosomal proteins (RPs) have been shown to be able to impart selectivity on the translating ribosome implicating them in gene expression control. Many ribosomal proteins are highly conserved and recently a number of ribosomal protein paralogs have been described in mammals. We examined the expression pattern of RPs in differentiating mouse Embryonic Stem Cells (ESCs), paying particular attention to the RP paralogs. We find the RP paralog Rpl39l is highly expressed in ESC and its expression strongly correlates with hepatocellular carcinoma tumor (HCC) samples with high tumor grading and alpha-fetoprotein level giving it diagnostic potential. We further screen the expression pattern of all RPs and their paralogs across 22 different tissues. We find that the more recently evolved RP paralogs show a much greater level of tissue-specific expression. We propose that these RP paralogs evolved more recently to provide a greater level of gene expression control to higher eukaryotes.

Indexed as

Agedalpha-FetoproteinsAnimalsCarcinoma, HepatocellularCell LineConserved SequenceEmbryonic Stem CellsEvolution, MolecularFemaleGene Expression Regulation, DevelopmentalGene Expression Regulation, NeoplasticHep G2 CellsHumansLiver NeoplasmsMaleMicealpha-FetoproteinsRibosomal Proteinshepatocellular carcinomaribosomal proteinribosomal protein paralogsRPL39L

Identifiers

PMID24452241
PMCPMC3929422
OpenAlexW2044621544

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.