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Mild Impairment of Learning and Memory in Mice Overexpressing the mSim2 Gene Located on Chromosome 16: An Animal Model of Down's Syndrome
- Source :
- Human Molecular Genetics. 8:1409-1415
- Publication Year :
- 1999
- Publisher :
- Oxford University Press (OUP), 1999.
-
Abstract
- Human Sim2 is a product of one of the genes located on human chromosome 21q22 and is a homolog of Drosophila single-minded ( sim ) which is a critical player in midline development of the central nervous system of the fly. Since Sim2 mRNA is expressed in facial, skull, palate and vertebra primordia in human and rodent embryos, features that are associated with phenotypes of Down's syndrome (DS), its trisomic state is suspected to contribute to the symptoms of DS. Here we describe that mSim2 mRNA is expressed in hippocampus and amygdala of adult mice, and that while mice overexpressing mSim2 under the control of the beta-actin promoter are viable and fertile and have superficially normal skeletal, brain and heart structures, they exhibit a moderate defect in context-dependent fear conditioning and a mild defect in the Morris water maze test. Taken together, our data show that overdosage of Sim2 may be important for the pathogenesis of Down's syndrome, especially mental retardation.
- Subjects :
- medicine.medical_specialty
Down syndrome
Genotype
Chromosomes, Human, Pair 21
Central nervous system
Morris water navigation task
Hippocampus
Mice, Transgenic
Motor Activity
Biology
Chromosomes
Mice
Chromosome 16
Internal medicine
Conditioning, Psychological
Basic Helix-Loop-Helix Transcription Factors
Genetics
medicine
Animals
Drosophila Proteins
Humans
Tissue Distribution
RNA, Messenger
Fear conditioning
Maze Learning
Molecular Biology
Swimming
Genetics (clinical)
Memory Disorders
Behavior, Animal
Learning Disabilities
Reverse Transcriptase Polymerase Chain Reaction
Nuclear Proteins
Fear
General Medicine
medicine.disease
DNA-Binding Proteins
Disease Models, Animal
Endocrinology
medicine.anatomical_structure
Gene Expression Regulation
SIM2
Down Syndrome
Trisomy
Subjects
Details
- ISSN :
- 14602083 and 09646906
- Volume :
- 8
- Database :
- OpenAIRE
- Journal :
- Human Molecular Genetics
- Accession number :
- edsair.doi.dedup.....bbe311f19e2bad9ff2a3f187af5c115a
- Full Text :
- https://doi.org/10.1093/hmg/8.8.1409