Evidence map›Paper›PMID 42263679›Full record

ArticleStem cell reports2026

Chromosome X dosage modulates development of aneuploidy in genetically diverse mouse embryonic stem cells.

Alexander Stanton, Selcan Aydin, Daniel A Skelly, Tracy McGarr, Dylan Stavish, Kim Leonhard, Seth Taapken, Tenneille Ludwig, Erik McIntire, Matthew Pankratz and 8 more

Abstract read
In one paragraph

Article in Stem cell reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

18 authors.

Alexander StantonThe Jackson Laboratory, Bar Harbor, ME 04609, USA; Tufts Graduate School of Biomedical Sciences, Tufts University School of Medicine, Boston, MA 021111, USA.
Selcan AydinThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Daniel A SkellyThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Tracy McGarrThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Dylan StavishDepartment of Biomedical Science, University of Sheffield, Western Bank, Sheffield S10 2TN, UK.
Kim LeonhardWiCell, Madison, WI 53719, USA.
Seth TaapkenWiCell, Madison, WI 53719, USA.
Tenneille LudwigWiCell, Madison, WI 53719, USA.
Erik McIntireDepartment of Human Genetics, the University of Chicago, Chicago, IL 60637, USA.
Matthew PankratzPredictive Biology Inc, Carlsbad, CA 92010, USA.
Anne CzechanskiThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
Ted ChoiPredictive Biology Inc, Carlsbad, CA 92010, USA.
Steven P GygiHarvard Medical School, Boston, MA 02115, USA.
Ivana BarbaricDepartment of Biomedical Science, University of Sheffield, Western Bank, Sheffield S10 2TN, UK.
Thomas VierbuchenDevelopmental Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering CancerCenter, New York, NY 10065, USA; Center for Stem Cell Biology, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Steven C MungerThe Jackson Laboratory, Bar Harbor, ME 04609, USA; Tufts Graduate School of Biomedical Sciences, Tufts University School of Medicine, Boston, MA 021111, USA.
Laura G ReinholdtThe Jackson Laboratory, Bar Harbor, ME 04609, USA; Tufts Graduate School of Biomedical Sciences, Tufts University School of Medicine, Boston, MA 021111, USA.
Martin F PeraThe Jackson Laboratory, Bar Harbor, ME 04609, USA; Tufts Graduate School of Biomedical Sciences, Tufts University School of Medicine, Boston, MA 021111, USA. Electronic address: martin.pera@jax.org.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

The genetic integrity of pluripotent stem cells (PSC) is critical to their applications in research and therapy, but it is compromised by frequent development of structural chromosome variants associated with malignancy. Many PSC lines exhibit remarkable genetic stability, but little is known about the basis of the known variation in genomic integrity among different PSC isolates. Here, we identify aneuploidies using RNA-seq and proteomics data from a panel of mouse embryonic stem cell (mESC) lines derived from 170 Diversity Outbred mice. We found 62 lines with detectable aneuploid subpopulations and a subset of originally XX lines that lost one chromosome X (XO). Strikingly, a much lower proportion of XX lines were aneuploid, compared to XY or XO lines. Two single-cell RNA-seq datasets demonstrated that aneuploid XY DO mESC also show lower chromosome X gene expression, and a prospective study confirmed that XY mESC accumulate higher aneuploid proportions in culture than isogenic XX lines. We identify potential mechanisms for this protective effect of X chromosome dosage, including our findings that the lines with two active X chromosomes have a higher proportion of 2-cell-like cells and higher expression of X-linked tumor suppressor genes, both features associated with the maintenance of genomic integrity, and that they compete more robustly in co-culture with chromosomally abnormal cells than XY cells.

Indexed as

AneuploidyGene DosageMouse Embryonic Stem CellsX ChromosomeAnimalsCell LineMice2C stateaneuploidycell competitione-karyotypingfemalegenetic integritymouse embryonic stem cellproteometranscriptomeX-chromosome

Identifiers

PMID42263679
PMCPMC13385727

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.