Evidence map›Paper›PMID 41081822›Full record

ReviewJournal of molecular evolution2025

A Multi-level Perspective on the Evolution of Orthologs and Their Functions.

Felix Langschied, Ruben Iruegas, Mateusz Sikora, Roberto Covino, Ingo Ebersberger

Abstract readReview
In one paragraph

Review in Journal of molecular evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Perspectives on Orthology During the Quest for Orthologs.Journal of molecular evolution · 2025
    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

5 authors.

Felix LangschiedInstitute of Cell Biology and Neuroscience, Applied Bioinformatics Group, Goethe University Frankfurt, Frankfurt am Main, Germany. langschied@bio.uni-frankfurt.de.ORCID 0009-0004-3348-3130
Ruben IruegasInstitute of Cell Biology and Neuroscience, Applied Bioinformatics Group, Goethe University Frankfurt, Frankfurt am Main, Germany.
Mateusz SikoraMalopolska Centre of Biotechnology, Jagiellonian University, Krakow, Poland.
Roberto CovinoInstitute of Computer Science, Goethe University Frankfurt, Frankfurt am Main, Germany.
Ingo EbersbergerInstitute of Cell Biology and Neuroscience, Applied Bioinformatics Group, Goethe University Frankfurt, Frankfurt am Main, Germany.ORCID 0000-0001-8187-9253

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Orthologs, evolutionarily related genes that diverged through speciation, are mutually the closest related sequences in different species. Consequently, they are ideal candidates for identifying functionally equivalent genes across taxa, a prerequisite for transferring gene function information from model to non-model organisms in silico. However, orthologs are not immune to functional divergence. Failing to recognize such divergent instances results in spurious functional annotation transfer. Here, we propose to treat the functional equivalence of orthologs as a null hypothesis that must be critically tested rather than assumed. This requires integrating several lines of evidence to evaluate both changes in an ortholog's network of molecular interactions and alterations in its biochemical activity. We outline how such activity shifts can be assessed using increasingly fine-grained analyses, including comparisons of protein feature architectures and predicted 3D structures. While some orthology resources incorporate aspects of this evidence, such assessments are often manual and not scalable. We argue for a systematic, multi-level perspective to detect functional divergence prior to annotation transfer. To support the broader adoption of this approach, we offer methodological recommendations and practical examples that demonstrate the value of this framework in large-scale comparative genomics.

Indexed as

Evolution, MolecularAnimalsComputational BiologyGenomicsHumansMolecular Sequence AnnotationAnnotation transferFeature architectureHomologyMetabolic pathwayProtein activityProtein domain

Identifiers

PMID41081822
PMCPMC12756255

What OpenQuestion holds

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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.