Expression of human-specific ARHGAP11B in mice leads to neocortex expansion and increased memory flexibility
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
MR/N004272/1
Medical Research Council - United Kingdom
PubMed
33938018
PubMed Central
PMC8246068
DOI
10.15252/embj.2020107093
Knihovny.cz E-zdroje
- Klíčová slova
- basal progenitors, brain evolution, human-specific gene, memory flexibility, neocortex expansion,
- MeSH
- biologická evoluce MeSH
- kognice fyziologie MeSH
- lidé MeSH
- myši inbrední C57BL MeSH
- myši transgenní MeSH
- myši MeSH
- neokortex metabolismus fyziologie MeSH
- neurogeneze fyziologie MeSH
- neurony metabolismus fyziologie MeSH
- paměť fyziologie MeSH
- proliferace buněk fyziologie MeSH
- proteiny aktivující GTPasu metabolismus MeSH
- úzkost metabolismus patofyziologie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- ARHGAP11B protein, human MeSH Prohlížeč
- proteiny aktivující GTPasu MeSH
Neocortex expansion during human evolution provides a basis for our enhanced cognitive abilities. Yet, which genes implicated in neocortex expansion are actually responsible for higher cognitive abilities is unknown. The expression of human-specific ARHGAP11B in embryonic/foetal mouse, ferret and marmoset neocortex was previously found to promote basal progenitor proliferation, upper-layer neuron generation and neocortex expansion during development, features commonly thought to contribute to increased cognitive abilities. However, a key question is whether this phenotype persists into adulthood and if so, whether cognitive abilities are indeed increased. Here, we generated a transgenic mouse line with physiological ARHGAP11B expression that exhibits increased neocortical size and upper-layer neuron numbers persisting into adulthood. Adult ARHGAP11B-transgenic mice showed altered neurobehaviour, notably increased memory flexibility and a reduced anxiety level. Our data are consistent with the notion that neocortex expansion by ARHGAP11B, a gene implicated in human evolution, underlies some of the altered neurobehavioural features observed in the transgenic mice, such as the increased memory flexibility, a neocortex-associated trait, with implications for the increase in cognitive abilities during human evolution.
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