Evidence map›Paper›PMID 39043684›Full record

ArticleNature communications2024

How antisense transcripts can evolve to encode novel proteins.

Bharat Ravi Iyengar, Anna Grandchamp, Erich Bornberg-Bauer

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Impact of GC content on de novo gene birth.Nature communications · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. The RNA Revolution in the Central Molecular Biology Dogma Evolution.International journal of molecular sciences · 2024
    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

3 authors.

Bharat Ravi IyengarInstitute for Evolution and Biodiversity, University of Münster, Hüfferstrasse 1, Münster, Germany. b.ravi@uni-muenster.de.ORCID 0000-0002-8983-4153
Anna GrandchampInstitute for Evolution and Biodiversity, University of Münster, Hüfferstrasse 1, Münster, Germany.
Erich Bornberg-BauerInstitute for Evolution and Biodiversity, University of Münster, Hüfferstrasse 1, Münster, Germany.ORCID 0000-0002-1826-3576

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) BO 2544/20-1Human Frontier Science Program (HFSP) RGP004/2023
6 · The paper itself

Abstract

Protein coding features can emerge de novo in non coding transcripts, resulting in emergence of new protein coding genes. Studies across many species show that a large fraction of evolutionarily novel non-coding RNAs have an antisense overlap with protein coding genes. The open reading frames (ORFs) in these antisense RNAs could also overlap with existing ORFs. In this study, we investigate how the evolution an ORF could be constrained by its overlap with an existing ORF in three different reading frames. Using a combination of mathematical modeling and genome/transcriptome data analysis in two different model organisms, we show that antisense overlap can increase the likelihood of ORF emergence and reduce the likelihood of ORF loss, especially in one of the three reading frames. In addition to rationalising the repeatedly reported prevalence of de novo emerged genes in antisense transcripts, our work also provides a generic modeling and an analytical framework that can be used to understand evolution of antisense genes.

Indexed as

Evolution, MolecularOpen Reading FramesRNA, AntisenseAnimalsModels, GeneticTranscriptomeRNA, Antisense

Identifiers

PMID39043684
PMCPMC11266595

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.