Evidence map›Paper›PMID 18479505›Full record

ArticleBiology direct2008

The look-ahead effect of phenotypic mutations.

Dion J Whitehead, Claus O Wilke, David Vernazobres, Erich Bornberg-Bauer

Abstract readComparative Study
In one paragraph

Article in Biology direct, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing 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

53 citing papers in PubMed.

  1. Article
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  4. Review
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  11. Article
  12. Exploring the expanse between theoretical questions and experimental approaches in the modern study of evolvability.Journal of experimental zoology. Part B, Molecular and developmental evolution · 2023
    Article
  13. Phenotypic mutations contribute to protein diversity and shape protein evolution.Protein science : a publication of the Protein Society · 2022
    Review
  14. Mechanisms of protein evolution.Protein science : a publication of the Protein Society · 2022
    Review
  15. Article
  16. Article
  17. The impact of mistranslation on phenotypic variability and fitness.Evolution; international journal of organic evolution · 2021
    Article
  18. Article
  19. Review
  20. 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.

Dion J WhiteheadInstitute for Evolution and Biodiversity, The Westphalian Wilhelms University of Muenster, 48149 Muenster, Germany. dion@uni-muenster.de
Claus O Wilke
David Vernazobres
Erich Bornberg-Bauer

Funding

Determinants of RNA virus evolutionR01AI065960 · NIAID · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI NOVELLA, ISABEL S · 2005 to 2009
$1.7M
NIAID NIH HHS AI 065960NIAID NIH HHS R01 AI065960
6 · The paper itself

Abstract

backgroundThe evolution of complex molecular traits such as disulphide bridges often requires multiple mutations. The intermediate steps in such evolutionary trajectories are likely to be selectively neutral or deleterious. Therefore, large populations and long times may be required to evolve such traits.

resultsWe propose that errors in transcription and translation may allow selection for the intermediate mutations, if the final trait provides a large enough selective advantage. We test this hypothesis using a population based model of protein evolution.

conclusionIf an individual acquires one of two mutations needed for a novel trait, the second mutation can be introduced into the phenotype due to transcription and translation errors. If the novel trait is advantageous enough, the allele with only one mutation will spread through the population, even though the gene sequence does not yet code for the complettrait. Thus, errors allow protein sequences to "look-ahead" for a more direct path to a complex trait.

Indexed as

Computer SimulationEvolution, MolecularModels, GeneticPhenotypeAllelesGenetics, PopulationMutationProtein BiosynthesisQuantitative Trait, HeritableSelection, GeneticTranscription, Genetic

Identifiers

PMID18479505
PMCPMC2423361

What OpenQuestion holds

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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.