Evidence map›Paper›PMID 37139943›Full record

ArticleMolecular biology and evolution2023

Evolutionary Trajectories of New Duplicated and Putative De Novo Genes.

José Carlos Montañés, Marta Huertas, Xavier Messeguer, M Mar Albà

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Impact of GC content on de novo gene birth.Nature communications · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. De Novo Genes: Current Status and Future Goals.Genome biology and evolution · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. De Novo Genes.Annual review of genetics · 2024
    Review
  12. Review
  13. Article
  14. De Novo Emerged Gene Search in Eukaryotes with DENSE.Genome biology and evolution · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
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

4 authors.

José Carlos MontañésEvolutionary Genomics Group, Research Programme on Biomedical Informatics, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.
Marta HuertasEvolutionary Genomics Group, Research Programme on Biomedical Informatics, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.
Xavier MesseguerComputer Sciences Department, Universitat Politècnica de Catalunya, Barcelona, Spain.
M Mar AlbàEvolutionary Genomics Group, Research Programme on Biomedical Informatics, Hospital del Mar Medical Research Institute (IMIM), Barcelona, Spain.ORCID 0000-0002-7963-7375

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The formation of new genes during evolution is an important motor of functional innovation, but the rate at which new genes originate and the likelihood that they persist over longer evolutionary periods are still poorly understood questions. Two important mechanisms by which new genes arise are gene duplication and de novo formation from a previously noncoding sequence. Does the mechanism of formation influence the evolutionary trajectories of the genes? Proteins arisen by gene duplication retain the sequence and structural properties of the parental protein, and thus they may be relatively stable. Instead, de novo originated proteins are often species specific and thought to be more evolutionary labile. Despite these differences, here we show that both types of genes share a number of similarities, including low sequence constraints in their initial evolutionary phases, high turnover rates at the species level, and comparable persistence rates in deeper branchers, in both yeast and flies. In addition, we show that putative de novo proteins have an excess of substitutions between charged amino acids compared with the neutral expectation, which is reflected in the rapid loss of their initial highly basic character. The study supports high evolutionary dynamics of different kinds of new genes at the species level, in sharp contrast with the stability observed at later stages.

Indexed as

Evolution, MolecularProteinsGene DuplicationPhylogenySaccharomyces cerevisiaeProteinsde novo genegene duplicationgene familyphylogeny

Identifiers

PMID37139943
PMCPMC10182736

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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.