Evidence map›Paper›PMID 41813158›Full record

ArticleProceedings of the Japan Academy. Series B, Physical and biological sciences2026

Highly polymorphic copy number variation in a segmental duplication in the mouse pseudoautosomal region even within inbred laboratory strains.

Takaoki Kasahara

Abstract read
In one paragraph

Article in Proceedings of the Japan Academy. Series B, Physical and biological sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. 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

1 author.

Takaoki KasaharaCareer Development Program, RIKEN Center for Brain Science.ORCID http://orcid.org/0000-0002-0953-5146

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inbred laboratory mice, such as the C57BL/6J strain, are presumed to be genetically uniform and are used in medical and biological research. Here, we report a substantial copy number variation (CNV) in a segmental duplication (SD) in the mouse pseudoautosomal region (PAR), which challenges the widely accepted assumption. The PAR consists of an identical sequence shared by the X and Y chromosomes at their distal ends, enabling proper pairing and recombination during meiosis. The copy number in C57BL/6J mice ranged from 4 to 27 per diploid genome. The mean (± standard deviation) was 12.9 ± 4.8. We found that de novo CNV emerged in nearly every spermatogenesis meiosis. The presence of CNV in the SD has also been detected in other classical inbred mouse strains. Each copy of the SD contains the Erdr1 gene. A correlation was observed between copy number and Erdr1 expression levels in males, and there was a significant negative correlation between expression level and body weight.

Indexed as

DNA Copy Number VariationsPolymorphism, GeneticPseudoautosomal RegionsSegmental Duplications, GenomicAnimalsMaleMiceMice, Inbred C57BLMice, Inbred StrainsC57BL/6Jde novo copy number variationmousepseudoautosomal regionsegmental duplication

Identifiers

PMID41813158
PMCPMC13050633

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Registered trials

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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.