Evidence map›Paper›PMID 15148580›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2004

A new role for expressed pseudogenes as ncRNA: regulation of mRNA stability of its homologous coding gene.

Yoshihisa Yano, Rintaro Saito, Noriyuki Yoshida, Atsushi Yoshiki, Anthony Wynshaw-Boris, Masaru Tomita, Shinji Hirotsune

Abstract read
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In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 72 citations in OpenAlex.

  1. Review
  2. Review
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  9. "Orphan" retrogenes in the human genome.Molecular biology and evolution · 2013
    Article
  10. Review
  11. Article
  12. Article
  13. HLA associations with nasopharyngeal carcinoma.Current molecular medicine · 2009
    Review
  14. Article
  15. Article
  16. Article
  17. The putatively functional Mkrn1-p1 pseudogene is neither expressed nor imprinted, nor does it regulate its source gene in trans.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
  18. Article
  19. Article
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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 4 institutions in 2 countries.

Yoshihisa YanoDepartment of Genetic Disease Research, Osaka City University Graduate School of Medicine, Asahi-machi 1-4-3 Abeno, 545-8585 Osaka, Japan.
Rintaro Saito
Noriyuki Yoshida
Atsushi Yoshiki
Anthony Wynshaw-Boris
Masaru Tomita
Shinji Hirotsune
Osaka City University · JPKeio University · JPRIKEN BioResource Research Center · JPUniversity of California, San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have earlier generated a mutant mouse in a course of making a transgenic line that exhibited interesting heterozygote phenotypes, which exhibited failure to thrive, severe bone deformities, and polycystic kidneys. This mutant mouse provided a clue to uncover a unique role of expressed pseudogenes. In this mutant the transgene was integrated into the vicinity of the expressing pseudogene of Makorin1 called Makorin1-p1. This insertion reduced transcription of the Makorin1-p1, resulting in destabilization of the Makorin1 mRNA in trans via a cis-acting RNA decay element within the 5' region of Makorin1 that is homologous between Makorin1 and Makorin1-p1. These findings demonstrate a novel and specific regulatory role of an expressed pseudogene as well as functional significance for noncoding RNAs. Next, we developed an original algorithm to determine how many pseudogenes are expressed. Based on our examination 2-3% of human processed pseudogenes are expressed using the most strict criteria. Interestingly, the mouse has a much smaller proportion of expressed pseudogenes (0.5-1%). Pseudogenes are functionally less constrained, and have accumulated more mutations than translated genes. If they have some functions in gene regulation, this property would allow more rapid functional diversification than protein-coding genes. In addition, some genetic phenomena that exhibit incomplete penetrance might be attributed to "mutation" or "variation" of pseudogenes.

Indexed as

Sequence Homology, Nucleic AcidAnimalsEmbryo, MammalianEmbryonic DevelopmentGene Expression Regulation, DevelopmentalMiceMice, TransgenicNerve Tissue ProteinsPseudogenesRibonucleoproteinsRNA StabilityMakorin ring finger protein 1Nerve Tissue ProteinsRibonucleoproteins

Identifiers

PMID15148580
OpenAlexW2109823109

What OpenQuestion holds

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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.