Literature DB >> 10400987

Mild impairment of learning and memory in mice overexpressing the mSim2 gene located on chromosome 16: an animal model of Down's syndrome.

M Ema1, S Ikegami, T Hosoya, J Mimura, H Ohtani, K Nakao, K Inokuchi, M Katsuki, Y Fujii-Kuriyama.   

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.

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Year:  1999        PMID: 10400987     DOI: 10.1093/hmg/8.8.1409

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  19 in total

1.  A novel binding protein of single-minded 2: the mitotic arrest-deficient protein MAD2B.

Authors:  Xianfang Meng; Xiujuan Tian; Xiaolan Wang; Pan Gao; Chun Zhang
Journal:  Neurogenetics       Date:  2012-06-02       Impact factor: 2.660

2.  Identification of a novel basic helix-loop-helix-PAS factor, NXF, reveals a Sim2 competitive, positive regulatory role in dendritic-cytoskeleton modulator drebrin gene expression.

Authors:  Norihisa Ooe; Koichi Saito; Nobuyoshi Mikami; Iwao Nakatuka; Hideo Kaneko
Journal:  Mol Cell Biol       Date:  2004-01       Impact factor: 4.272

3.  The proteins of human chromosome 21.

Authors:  Katheleen Gardiner; Alberto C S Costa
Journal:  Am J Med Genet C Semin Med Genet       Date:  2006-08-15       Impact factor: 3.908

4.  Sim2 prevents entry into the myogenic program by repressing MyoD transcription during limb embryonic myogenesis.

Authors:  Emmanuelle Havis; Pascal Coumailleau; Aline Bonnet; Keren Bismuth; Marie-Ange Bonnin; Randy Johnson; Chen-Min Fan; Frédéric Relaix; De-Li Shi; Delphine Duprez
Journal:  Development       Date:  2012-04-18       Impact factor: 6.868

5.  Sim2 mutants have developmental defects not overlapping with those of Sim1 mutants.

Authors:  Eleni Goshu; Hui Jin; Rachel Fasnacht; Mike Sepenski; Jacques L Michaud; Chen-Ming Fan
Journal:  Mol Cell Biol       Date:  2002-06       Impact factor: 4.272

6.  Generation of a panel of antibodies against proteins encoded on human chromosome 21.

Authors:  Frances K Wiseman; Olivia Sheppard; Jacqueline M Linehan; Sebastian Brandner; Victor L J Tybulewicz; Elizabeth M C Fisher
Journal:  J Negat Results Biomed       Date:  2010-08-20

7.  Identification of the transcription factor single-minded homologue 2 as a potential biomarker and immunotherapy target in prostate cancer.

Authors:  Mohamed S Arredouani; Bin Lu; Manoj Bhasin; Miriam Eljanne; Wen Yue; Juan-Miguel Mosquera; Glenn J Bubley; Vivian Li; Mark A Rubin; Towia A Libermann; Martin G Sanda
Journal:  Clin Cancer Res       Date:  2009-09-08       Impact factor: 12.531

Review 8.  Possible association of Down syndrome and exstrophy-epispadias complex: report of two new cases and review of the literature.

Authors:  Heiko Reutter; Arend Bökenkamp; Anne-Karolin Ebert; Wolfgang Rösch; Thomas M Boemers; Markus M Nöthen; Michael Ludwig
Journal:  Eur J Pediatr       Date:  2008-10-16       Impact factor: 3.183

9.  Noncoding sequences conserved in a limited number of mammals in the SIM2 interval are frequently functional.

Authors:  Kelly A Frazer; Heng Tao; Kazutoyo Osoegawa; Pieter J de Jong; Xiyin Chen; Mark F Doherty; David R Cox
Journal:  Genome Res       Date:  2004-02-12       Impact factor: 9.043

10.  Down syndrome and the molecular pathogenesis resulting from trisomy of human chromosome 21.

Authors:  Aarti Ruparelia; Frances Wiseman; Olivia Sheppard; Victor L J Tybulewicz; Elizabeth M C Fisher
Journal:  J Biomed Res       Date:  2010-03
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