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Sci Rep ; 7: 40284, 2017 01 10.
Article in English | MEDLINE | ID: mdl-28071689

ABSTRACT

Heterozygous mutations or deletions of the human Euchromatin Histone Methyltransferase 1 (EHMT1) gene are the main causes of Kleefstra syndrome, a neurodevelopmental disorder that is characterized by impaired memory, autistic features and mostly severe intellectual disability. Previously, Ehmt1+/- heterozygous knockout mice were found to exhibit cranial abnormalities and decreased sociability, phenotypes similar to those observed in Kleefstra syndrome patients. In addition, Ehmt1+/- knockout mice were impaired at fear extinction and novel- and spatial object recognition. In this study, Ehmt1+/- and wild-type mice were tested on several cognitive tests in a touchscreen-equipped operant chamber to further investigate the nature of learning and memory changes. Performance of Ehmt1+/- mice in the Visual Discrimination &Reversal learning, object-location Paired-Associates learning- and Extinction learning tasks was found to be unimpaired. Remarkably, Ehmt1+/- mice showed enhanced performance on the Location Discrimination test of pattern separation. In line with improved Location Discrimination ability, an increase in BrdU-labelled cells in the subgranular zone of the dentate gyrus was observed. In conclusion, reduced levels of EHMT1 protein in Ehmt1+/- mice does not result in general learning deficits in a touchscreen-based battery, but leads to increased adult cell proliferation in the hippocampus and enhanced pattern separation ability.


Subject(s)
Cognition Disorders/genetics , Craniofacial Abnormalities/genetics , Heart Defects, Congenital/genetics , Histone-Lysine N-Methyltransferase/genetics , Intellectual Disability/genetics , Learning/physiology , Animals , Cell Proliferation/genetics , Chromosome Deletion , Chromosomes, Human, Pair 9/genetics , Cognition Disorders/physiopathology , Craniofacial Abnormalities/physiopathology , Haploinsufficiency/genetics , Haploinsufficiency/physiology , Heart Defects, Congenital/physiopathology , Hippocampus/physiopathology , Humans , Intellectual Disability/physiopathology , Memory/physiology , Mice , Mice, Knockout , Mutation
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