Evidence map›Paper›PMID 36857092›Full record

ArticleMolecular biology and evolution2023

Evolution is not Uniform Along Coding Sequences.

Raphaël Bricout, Dominique Weil, David Stroebel, Auguste Genovesio, Hugues Roest Crollius

Erratum issuedAbstract 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. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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  10. The fitness cost of spurious phosphorylation.bioRxiv : the preprint server for biology · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Raphaël BricoutDépartement de biologie, École normale supérieure, Institut de Biologie de l'ENS (IBENS), CNRS, INSERM, Paris, France.
Dominique WeilLaboratoire de Biologie du Développement, Sorbonne Université, CNRS, Institut de Biologie Paris-Seine (IBPS), Paris, France.
David StroebelDépartement de biologie, École normale supérieure, Institut de Biologie de l'ENS (IBENS), CNRS, INSERM, Paris, France.
Auguste GenovesioDépartement de biologie, École normale supérieure, Institut de Biologie de l'ENS (IBENS), CNRS, INSERM, Paris, France.
Hugues Roest CrolliusDépartement de biologie, École normale supérieure, Institut de Biologie de l'ENS (IBENS), CNRS, INSERM, Paris, France.ORCID 0000-0002-8209-173X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amino acids evolve at different speeds within protein sequences, because their functional and structural roles are different. Notably, amino acids located at the surface of proteins are known to evolve more rapidly than those in the core. In particular, amino acids at the N- and C-termini of protein sequences are likely to be more exposed than those at the core of the folded protein due to their location in the peptidic chain, and they are known to be less structured. Because of these reasons, we would expect that amino acids located at protein termini would evolve faster than residues located inside the chain. Here we test this hypothesis and found that amino acids evolve almost twice as fast at protein termini compared with those in the center, hinting at a strong topological bias along the sequence length. We further show that the distribution of solvent-accessible residues and functional domains in proteins readily explain how structural and functional constraints are weaker at their termini, leading to the observed excess of amino acid substitutions. Finally, we show that the specific evolutionary rates at protein termini may have direct consequences, notably misleading in silico methods used to infer sites under positive selection within genes. These results suggest that accounting for positional information should improve evolutionary models.

Indexed as

Amino AcidsProteinsAmino Acid SequenceAmino Acid SubstitutionEvolution, MolecularExonsAmino AcidsProteins

Identifiers

PMID36857092
PMCPMC10025431

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Registered trials

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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.