Evidence map›Paper›PMID 36649207›Full record

ArticleG3 (Bethesda, Md.)2023

Protein coding variation in the J:ARC and J:DO outbred laboratory mouse stocks provides a molecular basis for distinct research applications.

Belinda K Cornes, Carolyn Paisie, Emily Swanzey, Peter D Fields, Andrew Schile, Kelly Brackett, Laura G Reinholdt, Anuj Srivastava

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 26% of its field
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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 1 institution in 1 country.

Belinda K CornesMammalian Genetics, The Jackson Laboratory, 600 Main Street, USA.
Carolyn PaisieMammalian Genetics, The Jackson Laboratory, 600 Main Street, USA.
Emily SwanzeyMammalian Genetics, The Jackson Laboratory, 600 Main Street, USA.
Peter D FieldsMammalian Genetics, The Jackson Laboratory, 600 Main Street, USA.
Andrew SchileMammalian Genetics, The Jackson Laboratory, 600 Main Street, USA.
Kelly BrackettMammalian Genetics, The Jackson Laboratory, 600 Main Street, USA.
Laura G ReinholdtMammalian Genetics, The Jackson Laboratory, 600 Main Street, USA.ORCID 0000-0003-4054-4048
Anuj SrivastavaMammalian Genetics, The Jackson Laboratory, 600 Main Street, USA.
Jackson Laboratory · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
The Mutant Mouse Resource and Research Center at The Jackson LaboratoryU42OD010921 · OD · JACKSON LABORATORY · PI LAURA G REINHOLDT · 2012 to 2026
$21.4M
Use for ResourceP40OD011102 · OD · JACKSON LABORATORY · PI Steven Carmen Munger, Stephen A Murray · 2012 to 2026
$15.0M
Resources for Comparative Mendelian Disease GenomicsR24OD021325 · OD · JACKSON LABORATORY · PI BERGSTROM, DAVID ERIC, REINHOLDT, LAURA G · 2016 to 2023
$6.5M
Genetically Diverse Mouse Embryonic Stem Cells: A Platform for Cellular Systems GeneticsR24OD030037 · OD · JACKSON LABORATORY · PI BAKER, CHRISTOPHER LEE, MUNGER, STEVEN CARMEN · 2021 to 2024
$3.2M
NCI NIH HHS P30 CA034196NIH HHS P40 OD011102NIH HHS R24 OD021325NIH HHS R24 OD030037NIH HHS U42 OD010921
6 · The paper itself

Abstract

Outbred laboratory mice (Mus musculus) are readily available and have high fecundity, making them a popular choice in biomedical research, especially toxicological and pharmacological applications. Direct high throughput genome sequencing (HTS) of these widely used research animals is an important genetic quality control measure that enhances research reproducibility. HTS data have been used to confirm the common origin of outbred stocks and to molecularly define distinct outbred populations. But these data have also revealed unexpected population structure and homozygosity in some populations; genetic features that emerge when outbred stocks are not properly maintained. We used exome sequencing to discover and interrogate protein-coding variation in a newly established population of Swiss-derived outbred stock (J:ARC) that is closely related to other, commonly used CD-1 outbred populations. We used these data to describe the genetic architecture of the J:ARC population including heterozygosity, minor allele frequency, LD decay, and we defined novel, protein-coding sequence variation. These data reveal the expected genetic architecture for a properly maintained outbred stock and provide a basis for the on-going genetic quality control. We also compared these data to protein-coding variation found in a multiparent outbred stock, the Diversity Outbred (J:DO). We found that the more recently derived, multiparent outbred stock has significantly higher interindividual variability, greater overall genetic variation, higher heterozygosity, and fewer novel variants than the Swiss-derived J:ARC stock. However, among the novel variants found in the J:DO stock, significantly more are predicted to be protein-damaging. The fact that individuals from this population can tolerate a higher load of potentially damaging variants highlights the buffering effects of allelic diversity and the differing selective pressures in these stocks. While both outbred stocks offer significant individual heterozygosity, our data provide a molecular basis for their intended applications, where the J:DO are best suited for studies requiring maximum, population-level genetic diversity and power for mapping, while the J:ARC are best suited as a general-purpose outbred stock with robust fecundity, relatively low allelic diversity, and less potential for extreme phenotypic variability.

Indexed as

Genetic VariationAllelesAnimalsGene FrequencyHeterozygoteHomozygoteMiceReproducibility of Resultsexomegenetic quality controllaboratory miceoutbred stocksreproducibility

Identifiers

PMID36649207
PMCPMC10085793
OpenAlexW4316928637

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.