Evidence map›Paper›PMID 25157146›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Comparative analysis of pseudogenes across three phyla.

Cristina Sisu, Baikang Pei, Jing Leng, Adam Frankish, Yan Zhang, Suganthi Balasubramanian, Rachel Harte, Daifeng Wang, Michael Rutenberg-Schoenberg, Wyatt Clark and 5 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
7.5field-weighted citation impact, top 3% 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

64 citing papers in PubMed, 107 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Retention of a singlebioRxiv : the preprint server for biology · 2025
    Article
  6. Systematic analysis of noncanonical ribosomal protein paralogs does not provide evidence for specialized functions inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Gene-Pseudogene Inversions as a Hidden Source of Missing Heritability.medRxiv : the preprint server for health sciences · 2025
    Article
  9. Article
  10. Pseudogenes in the carcinogenesis: epithelial-to-mesenchymal transition process and cancer initiating cells.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2025
    Review
  11. The reconstruction of evolutionary dynamics of processed pseudogenes indicates deep silencing of "retrobiome" in naked mole rat.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. The annotation ofScience advances · 2024
    Article
  13. The physical and evolutionary energy landscapes of devolved protein sequences corresponding to pseudogenes.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Article
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  19. Article
  20. Extensive nrDNA ITS polymorphism inFrontiers in plant science · 2022
    Article

4 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

15 authors at 3 institutions in 2 countries.

Cristina SisuProgram in Computational Biology and Bioinformatics and Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520;
Baikang PeiProgram in Computational Biology and Bioinformatics and.
Jing LengProgram in Computational Biology and Bioinformatics and.
Adam FrankishWellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom;
Yan ZhangProgram in Computational Biology and Bioinformatics and.
Suganthi BalasubramanianDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520;
Rachel HarteCenter for Biomolecular Science and Engineering, University of California, Santa Cruz, CA 95064; and.
Daifeng WangProgram in Computational Biology and Bioinformatics and.
Michael Rutenberg-SchoenbergProgram in Computational Biology and Bioinformatics and.
Wyatt ClarkProgram in Computational Biology and Bioinformatics and.
Mark DiekhansCenter for Biomolecular Science and Engineering, University of California, Santa Cruz, CA 95064; and.
Joel RozowskyDepartment of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520;
Tim HubbardWellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom;
Jennifer HarrowWellcome Trust Sanger Institute, Cambridge CB10 1SA, United Kingdom;
Mark B GersteinProgram in Computational Biology and Bioinformatics and Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520; Department of Computer Science, Yale University, New Haven, CT 06511 mark@gersteinlab.org.
Yale University · USWellcome Sanger Institute · GBUniversity of California, Santa Cruz · US

Funding

Skill Development for Diverse Scientific Careers: A New Course Predoctoral Program in Cellular and Molecular BiologyT32GM007223 · NIGMS · YALE UNIVERSITY · PI BASERGA, SUSAN J · 1985 to 2019
$31.0M
MEDICAL INFORMATICS RESEARCH TRAINING AT YALET15LM007056 · NLM · YALE UNIVERSITY · PI Mark Bender Gerstein, LUCILA OHNO-MACHADO · 1987 to 2026
$22.2M
GENCODE Resource ProjectU41HG007234 · NHGRI · SANGER INSTITUTE · PI FLICEK, PAUL · 2013 to 2020
$20.3M
NHGRI NIH HHS U41 HG007234NIGMS NIH HHS T32 GM007223NLM NIH HHS T15 LM007056
6 · The paper itself

Abstract

Pseudogenes are degraded fossil copies of genes. Here, we report a comparison of pseudogenes spanning three phyla, leveraging the completed annotations of the human, worm, and fly genomes, which we make available as an online resource. We find that pseudogenes are lineage specific, much more so than protein-coding genes, reflecting the different remodeling processes marking each organism's genome evolution. The majority of human pseudogenes are processed, resulting from a retrotranspositional burst at the dawn of the primate lineage. This burst can be seen in the largely uniform distribution of pseudogenes across the genome, their preservation in areas with low recombination rates, and their preponderance in highly expressed gene families. In contrast, worm and fly pseudogenes tell a story of numerous duplication events. In worm, these duplications have been preserved through selective sweeps, so we see a large number of pseudogenes associated with highly duplicated families such as chemoreceptors. However, in fly, the large effective population size and high deletion rate resulted in a depletion of the pseudogene complement. Despite large variations between these species, we also find notable similarities. Overall, we identify a broad spectrum of biochemical activity for pseudogenes, with the majority in each organism exhibiting varying degrees of partial activity. In particular, we identify a consistent amount of transcription (∼15%) across all species, suggesting a uniform degradation process. Also, we see a uniform decay of pseudogene promoter activity relative to their coding counterparts and identify a number of pseudogenes with conserved upstream sequences and activity, hinting at potential regulatory roles.

Indexed as

PhylogenyAnimalsCaenorhabditis elegansDrosophila melanogasterEvolution, MolecularGenetic Association StudiesHumansMolecular Sequence AnnotationPromoter Regions, GeneticPseudogenesSequence Homology, Nucleic Acidfunctional genomicsgenome annotationtranscriptomics

Identifiers

PMID25157146
PMCPMC4169933
OpenAlexW2087347094

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.