Evidence map›Paper›PMID 34464968›Full record

ArticleMolecular biology and evolution2021

A Positively Selected MAGEE2 LoF Allele Is Associated with Sexual Dimorphism in Human Brain Size and Shows Similar Phenotypes in Magee2 Null Mice.

Michał Szpak, Stephan C Collins, Yan Li, Xiao Liu, Qasim Ayub, Marie-Christine Fischer, Valerie E Vancollie, Christopher J Lelliott, Yali Xue, Binnaz Yalcin and 2 more

Open access · goldAbstract read
In one paragraph

Article in Molecular biology and evolution, 2021. 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
0.1field-weighted citation impact, top 56% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  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

12 authors at 5 institutions in 4 countries.

Michał SzpakWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.ORCID 0000-0002-9096-852X
Stephan C CollinsInserm UMR1231, Genetics of Developmental Disorders Laboratory, University of Bourgogne Franche-Comté, Dijon, France.
Yan LiBGI-Shenzhen, Shenzhen, China.
Xiao LiuTsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen, China.
Qasim AyubWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Marie-Christine FischerIGBMC, UMR7104, Illkirch, Inserm, France.
Valerie E VancollieWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.ORCID 0000-0003-1547-1975
Christopher J LelliottWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Yali XueWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Binnaz YalcinInserm UMR1231, Genetics of Developmental Disorders Laboratory, University of Bourgogne Franche-Comté, Dijon, France.
Huanming YangBGI-Shenzhen, Shenzhen, China.
Chris Tyler-SmithWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Wellcome Sanger Institute · GBInserm · FRBGI Group (China) · CNMonash University Malaysia · MYTsinghua–Berkeley Shenzhen Institute · CN

Funding

Wellcome WT098051Wellcome Trust 206194
6 · The paper itself

Abstract

A nonsense allele at rs1343879 in human MAGEE2 on chromosome X has previously been reported as a strong candidate for positive selection in East Asia. This premature stop codon causing ∼80% protein truncation is characterized by a striking geographical pattern of high population differentiation: common in Asia and the Americas (up to 84% in the 1000 Genomes Project East Asians) but rare elsewhere. Here, we generated a Magee2 mouse knockout mimicking the human loss-of-function mutation to study its functional consequences. The Magee2 null mice did not exhibit gross abnormalities apart from enlarged brain structures (13% increased total brain area, P = 0.0022) in hemizygous males. The area of the granular retrosplenial cortex responsible for memory, navigation, and spatial information processing was the most severely affected, exhibiting an enlargement of 34% (P = 3.4×10-6). The brain size in homozygous females showed the opposite trend of reduced brain size, although this did not reach statistical significance. With these insights, we performed human association analyses between brain size measurements and rs1343879 genotypes in 141 Chinese volunteers with brain MRI scans, replicating the sexual dimorphism seen in the knockout mouse model. The derived stop gain allele was significantly associated with a larger volume of gray matter in males (P = 0.00094), and smaller volumes of gray (P = 0.00021) and white (P = 0.0015) matter in females. It is unclear whether or not the observed neuroanatomical phenotypes affect behavior or cognition, but it might have been the driving force underlying the positive selection in humans.

Indexed as

BrainSex CharacteristicsAllelesAnimalsAntigens, NeoplasmFemaleHumansIntracellular Signaling Peptides and ProteinsIntrinsically Disordered ProteinsMaleMiceMice, KnockoutOrgan SizePhenotypeProteinsAntigens, NeoplasmIntracellular Signaling Peptides and ProteinsIntrinsically Disordered ProteinsMAGEL2 protein, humanMagel2 protein, mouseProteinsbrain sizeloss of functionmouse knockoutMRIpositive selectionsexual dimorphism

Identifiers

PMID34464968
PMCPMC8662591
OpenAlexW3196296811

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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.