Evidence map›Paper›PMID 33865332›Full record

ArticleBMC genomics2021

Population and subspecies diversity at mouse centromere satellites.

Uma P Arora, Caleigh Charlebois, Raman Akinyanju Lawal, Beth L Dumont

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 29 citations in OpenAlex.

  1. Cross-species incompatibilities offer new insights into the functional consequences of satellite DNA evolution.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2026
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  10. Centromere regulation in the germline and early embryo.Current opinion in genetics & development · 2025
    Review
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  20. Meiotic drive in house mice: mechanisms, consequences, and insights for human biology.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2022
    Review
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

4 authors at 2 institutions in 1 country.

Uma P AroraThe Jackson Laboratory, 600 Main Street, Bar Harbor, ME, 04609, USA. Uma.Arora@jax.org.ORCID http://orcid.org/0000-0002-3598-5386
Caleigh CharleboisThe Jackson Laboratory, 600 Main Street, Bar Harbor, ME, 04609, USA.
Raman Akinyanju LawalThe Jackson Laboratory, 600 Main Street, Bar Harbor, ME, 04609, USA.
Beth L DumontThe Jackson Laboratory, 600 Main Street, Bar Harbor, ME, 04609, USA. Beth.Dumont@jax.org.
Jackson Laboratory · USTufts University · US

Funding

Population genomics in laboratory and outbred mouse populationsR35GM133415 · NIGMS · JACKSON LABORATORY · PI BETHANY L DUMONT · 2019 to 2026
$3.1M
Jackson Laboratory Scholar AwardNational Institute of Child Health and Human Development T32National Science Foundation DBI-1851697NIGMS NIH HHS R35NIGMS NIH HHS R35 GM133415
6 · The paper itself

Abstract

backgroundMammalian centromeres are satellite-rich chromatin domains that execute conserved roles in kinetochore assembly and chromosome segregation. Centromere satellites evolve rapidly between species, but little is known about population-level diversity across these loci.

resultsWe developed a k-mer based method to quantify centromere copy number and sequence variation from whole genome sequencing data. We applied this method to diverse inbred and wild house mouse (Mus musculus) genomes to profile diversity across the core centromere (minor) satellite and the pericentromeric (major) satellite repeat. We show that minor satellite copy number varies more than 10-fold among inbred mouse strains, whereas major satellite copy numbers span a 3-fold range. In contrast to widely held assumptions about the homogeneity of mouse centromere repeats, we uncover marked satellite sequence heterogeneity within single genomes, with diversity levels across the minor satellite exceeding those at the major satellite. Analyses in wild-caught mice implicate subspecies and population origin as significant determinants of variation in satellite copy number and satellite heterogeneity. Intriguingly, we also find that wild-caught mice harbor dramatically reduced minor satellite copy number and elevated satellite sequence heterogeneity compared to inbred strains, suggesting that inbreeding may reshape centromere architecture in pronounced ways.

conclusionTaken together, our results highlight the power of k-mer based approaches for probing variation across repetitive regions, provide an initial portrait of centromere variation across Mus musculus, and lay the groundwork for future functional studies on the consequences of natural genetic variation at these essential chromatin domains.

Indexed as

CentromereDNA, SatelliteAnimalsMiceMice, Inbred StrainsRepetitive Sequences, Nucleic AcidDNA, SatelliteBioinformaticsCENP-ACentromereEvolutionGenetic diversityInbred micek-merMammalian genomicsSatellite DNAWild mice

Identifiers

PMID33865332
PMCPMC8052823
OpenAlexW3156824491

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.