Evidence map›Paper›PMID 23153069›Full record

ArticleGenome biology2012

Evidence for conserved post-transcriptional roles of unitary pseudogenes and for frequent bifunctionality of mRNAs.

Ana C Marques, Jennifer Tan, Sheena Lee, Lesheng Kong, Andreas Heger, Chris P Ponting

Abstract read
In one paragraph

Article in Genome biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

41 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Identification and Analysis ofFrontiers in aging neuroscience · 2022
    Article
  6. Crucial Roles of miR-625 in Human Cancer.Frontiers in medicine · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Non-Coding RNAs and their Integrated Networks.Journal of integrative bioinformatics · 2019
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Complexities of post-transcriptional regulation and the modeling of ceRNA crosstalk.Critical reviews in biochemistry and molecular biology · 2018
    Review
  18. Interaction and cross-talk between non-coding RNAs.Cellular and molecular life sciences : CMLS · 2018
    Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Ana C Marques
Jennifer Tan
Sheena Lee
Lesheng Kong
Andreas Heger
Chris P Ponting

Funding

Medical Research Council MC_U137761446
6 · The paper itself

Abstract

backgroundRecent reports have highlighted instances of mRNAs that, in addition to coding for protein, regulate the abundance of related transcripts by altering microRNA availability. These two mRNA roles - one mediated by RNA and the other by protein - are inter-dependent and hence cannot easily be separated. Whether the RNA-mediated role of transcripts is important, per se, or whether it is a relatively innocuous consequence of competition by different transcripts for microRNA binding remains unknown.

resultsHere we took advantage of 48 loci that encoded proteins in the earliest eutherian ancestor, but whose protein-coding capability has since been lost specifically during rodent evolution. Sixty-five percent of such loci, which we term 'unitary pseudogenes', have retained their expression in mouse and their transcripts exhibit conserved tissue expression profiles. The maintenance of these unitary pseudogenes' spatial expression profiles is associated with conservation of their microRNA response elements and these appear to preserve the post-transcriptional roles of their protein-coding ancestor. We used mouse Pbcas4, an exemplar of these transcribed unitary pseudogenes, to experimentally test our genome-wide predictions. We demonstrate that the role of Pbcas4 as a competitive endogenous RNA has been conserved and has outlived its ancestral gene's loss of protein-coding potential.

conclusionsThese results show that post-transcriptional regulation by bifunctional mRNAs can persist over long evolutionary time periods even after their protein coding ability has been lost.

Indexed as

Conserved SequencePseudogenesAnimalsBase SequenceCell LineDogsGene Expression ProfilingHumansMiceMicroRNAsMolecular Sequence DataPhylogenyRNA, MessengerRNA Processing, Post-TranscriptionalRodentiaMicroRNAsRNA, Messenger

Identifiers

PMID23153069
PMCPMC3580494

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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.