TY - JOUR
T1 - Mild impairment of learning and memory in mice overexpressing the mSim2 gene located on chromosome 16
T2 - An animal model of Down's syndrome
AU - Ema, Masatsugu
AU - Ikegami, Shiro
AU - Hosoya, Tomonori
AU - Mimura, Junsei
AU - Ohtani, Haruo
AU - Nakao, Kazuki
AU - Inokuchi, Kaoru
AU - Katsuki, Motoya
AU - Fujii-Kuriyama, Yoshiaki
N1 - Funding Information:
This work was supported in part by Grants-in-Aid for Scientific Research on Priority Areas, and for Scientific Research (B) from the Ministry of Education, Culture, Sport and Science of Japan, and by a fund from Sankyo Co. M.E. is a research fellow of the Japan Society for the Promotion of Science.
PY - 1999
Y1 - 1999
N2 - 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 β-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.
AB - 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 β-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.
UR - http://www.scopus.com/inward/record.url?scp=0032837516&partnerID=8YFLogxK
U2 - 10.1093/hmg/8.8.1409
DO - 10.1093/hmg/8.8.1409
M3 - 学術論文
C2 - 10400987
AN - SCOPUS:0032837516
SN - 0964-6906
VL - 8
SP - 1409
EP - 1415
JO - Human Molecular Genetics
JF - Human Molecular Genetics
IS - 8
ER -