Evidence map›Paper›PMID 41014119›Full record

ArticleGenetics2025

The impact of non-neutral synonymous mutations when inferring selection on nonsynonymous mutations.

Aina Martinez I Zurita, Christopher C Kyriazis, Kirk E Lohmueller

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Article in Genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing 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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Aina Martinez I ZuritaDepartment of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA 90095-1606, United States.ORCID 0000-0001-9300-872X
Christopher C KyriazisDepartment of Ecology and Evolutionary Biology, University of California, Los Angeles, CA 90095-1606, United States.
Kirk E LohmuellerDepartment of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA 90095-1606, United States.ORCID 0000-0002-3874-369X

Funding

Population genomics of the selective effects of new mutationsR35GM119856 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI LOHMUELLER, KIRK · 2016 to 2025
$3.4M
NIGMS NIH HHS R35 GM119856NIH HHS R35GM119856
6 · The paper itself

Abstract

The distribution of fitness effects (DFE) describes the proportions of new mutations that have different effects on fitness. Accurate measurements of the DFE are important because the DFE is a fundamental parameter in evolutionary genetics and has implications for understanding of other phenomena such as complex disease or inbreeding depression. Current computational methods to infer the DFE for nonsynonymous mutations from natural variation first estimate demographic parameters from synonymous variants to control for the effects of demography and background selection. Then, conditional on these parameters, the DFE is inferred for nonsynonymous mutations. This approach relies on the assumption that synonymous variants are neutrally evolving. However, some evidence points toward synonymous mutations having measurable effects on fitness. To test whether selection on synonymous mutations affects inference of the DFE of nonsynonymous mutations, we simulated several possible models of selection on synonymous mutations using SLiM and attempted to recover the DFE of nonsynonymous mutations using Fit∂a∂i, a common method for DFE inference. Our results show that the presence of selection on synonymous variants leads to incorrect inferences of recent population growth. Furthermore, under certain parameter combinations with pervasive selection on synonymous mutations, the inferred DFEs for nonsynonymous mutations show an inflated proportion of highly deleterious and nearly neutral mutations. However, this bias can be eliminated if the correct demographic parameters are used for DFE inference instead of the biased ones inferred from synonymous variants. Our work demonstrates how unmodeled selection on synonymous mutations may affect downstream inferences of the DFE.

Indexed as

Genetic FitnessModels, GeneticMutationSelection, GeneticSilent MutationComputer SimulationEvolution, MolecularGenetics, Populationdemographic inferenceDFEpopulation geneticssynonymous mutations

Identifiers

PMID41014119
PMCPMC12693584

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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.