Evidence map›Paper›PMID 39101589›Full record

ArticleMolecular biology and evolution2024

Variation in the Spectrum of New Mutations among Inbred Strains of Mice.

Eugenio López-Cortegano, Jobran Chebib, Anika Jonas, Anastasia Vock, Sven Künzel, Diethard Tautz, Peter D Keightley

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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  7. Increased rate ofbioRxiv : the preprint server for biology · 2025
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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

7 authors.

Eugenio López-CorteganoInstitute of Ecology and Evolution, University of Edinburgh, Edinburgh, EH9 3FL, UK.ORCID 0000-0001-6914-6305
Jobran ChebibInstitute of Ecology and Evolution, University of Edinburgh, Edinburgh, EH9 3FL, UK.ORCID 0000-0003-0573-6837
Anika JonasDepartment for Evolutionary Genetics, Max Planck Institute for Evolutionary Biology, 24306 Plön, Germany.
Anastasia VockDepartment for Evolutionary Genetics, Max Planck Institute for Evolutionary Biology, 24306 Plön, Germany.
Sven KünzelDepartment for Evolutionary Genetics, Max Planck Institute for Evolutionary Biology, 24306 Plön, Germany.
Diethard TautzDepartment for Evolutionary Genetics, Max Planck Institute for Evolutionary Biology, 24306 Plön, Germany.ORCID 0000-0002-0460-5344
Peter D KeightleyInstitute of Ecology and Evolution, University of Edinburgh, Edinburgh, EH9 3FL, UK.ORCID 0000-0001-8129-2794

Funding

European Research Council 694212
6 · The paper itself

Abstract

The mouse serves as a mammalian model for understanding the nature of variation from new mutations, a question that has both evolutionary and medical significance. Previous studies suggest that the rate of single-nucleotide mutations (SNMs) in mice is ∼50% of that in humans. However, information largely comes from studies involving the C57BL/6 strain, and there is little information from other mouse strains. Here, we study the mutations that accumulated in 59 mouse lines derived from four inbred strains that are commonly used in genetics and clinical research (BALB/cAnNRj, C57BL/6JRj, C3H/HeNRj, and FVB/NRj), maintained for eight to nine generations by brother-sister mating. By analyzing Illumina whole-genome sequencing data, we estimate that the average rate of new SNMs in mice is ∼μ = 6.7 × 10-9. However, there is substantial variation in the spectrum of SNMs among strains, so the burden from new mutations also varies among strains. For example, the FVB strain has a spectrum that is markedly skewed toward C→A transversions and is likely to experience a higher deleterious load than other strains, due to an increased frequency of nonsense mutations in glutamic acid codons. Finally, we observe substantial variation in the rate of new SNMs among DNA sequence contexts, CpG sites, and their adjacent nucleotides playing an important role.

Indexed as

Mice, Inbred StrainsAnimalsMiceMice, Inbred C57BLMutationMus musculusmutation accumulationmutation ratemutation spectrum

Identifiers

PMID39101589
PMCPMC11327921

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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.