Mice trisomic for a bacterial artificial chromosome with the single-minded 2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome

被引:87
作者
Chrast, R
Scott, HS
Madani, R
Huber, L
Wolfer, DP
Prinz, M
Aguzzi, A
Lipp, HP
Antonarakis, SE
机构
[1] Univ Geneva, Sch Med, Div Med Genet, CH-1211 Geneva 4, Switzerland
[2] Univ Hosp, CH-1211 Geneva, Switzerland
[3] Univ Geneva, Sch Med, Grad Program Cellular & Mol Biol, CH-1211 Geneva 4, Switzerland
[4] Univ Zurich, Inst Anat, Zurich, Switzerland
[5] Univ Zurich Hosp, Inst Neuropathol, CH-8091 Zurich, Switzerland
关键词
D O I
10.1093/hmg/9.12.1853
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Drosophila single-minded (sim) transcription factor, is a master regulator of fruitfly neurogenesis. Recently, we have cloned and mapped a human homolog of sim, SIM2,to chromosome 21 in the so-called 'Down syndrome chromosomal region'. Three copies of SIM2 may contribute to some Down syndrome (DS) phenotypes because of the mapping position function as transcriptional repressor, temporal and spatial expression pattern of mouse Sim2, and the potentially analogous role of human SIM2 to that of Drosophila sim during neurogenesis. In order to validate this hypothesis in vivo, we have created the first bacterial artificial chromosome transgenic mice overexpressing a gene possibly involved in DS with only one or two additional copies of mouse Sim2, The transgene was shown to be expressed in the same spatial pattern as the endogenous gene. The mice develop normally, are fertile and do not show detectable histopathological abnormalities. However, detailed analysis of their behavior revealed anxiety-related/reduced exploratory behaviour and sensitivity to pain, phenotypes similar to those also present in other partial trisomy 16 mouse models of DS, Our data therefore suggest that overexpression of SIM2 contributes to some of the complex DS phenotypes.
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页码:1853 / 1864
页数:12
相关论文
共 39 条
[21]   Pain responses, anxiety and aggression in mice deficient in pre-proenkephalin [J].
Konig, M ;
Zimmer, AM ;
Steiner, H ;
Holmes, PV ;
Crawley, JN ;
Brownstein, MJ ;
Zimmer, A .
NATURE, 1996, 383 (6600) :535-538
[22]  
LEJEUNE J, 1959, CR HEBD ACAD SCI, V248, P1721
[23]   Gene dosage in mice - BAC to the future [J].
Magdaleno, SM ;
Curran, T .
NATURE GENETICS, 1999, 22 (04) :319-320
[24]   A murine model for Down syndrome shows reduced responsiveness to pain [J].
Martínez-Cué, C ;
Baamonde, C ;
Lumbreras, MA ;
Vallina, IF ;
Dierssen, M ;
Flórez, J .
NEUROREPORT, 1999, 10 (05) :1119-1122
[25]   MOLECULAR GENETIC APPROACH TO THE CHARACTERIZATION OF THE DOWN SYNDROME REGION OF CHROMOSOME-21 [J].
MCCORMICK, MK ;
SCHINZEL, A ;
PETERSEN, MB ;
STETTEN, G ;
DRISCOLL, DJ ;
CANTU, ES ;
TRANEBJAERG, L ;
MIKKELSEN, M ;
WATKINS, PC ;
ANTONARAKIS, SE .
GENOMICS, 1989, 5 (02) :325-331
[26]   Essential role for TrkB receptors in hippocampus-mediated learning [J].
Minichiello, L ;
Korte, M ;
Wolfer, D ;
Kühn, R ;
Unsicker, K ;
Cestari, V ;
Rossi-Arnaud, C ;
Lipp, HP ;
Bonhoeffer, T ;
Klein, R .
NEURON, 1999, 24 (02) :401-414
[27]   Characterization of msim, a murine homologue of the Drosophila sim transcription factor [J].
Moffett, P ;
Dayo, M ;
Reece, M ;
McCormick, MK ;
Pelletier, J .
GENOMICS, 1996, 35 (01) :144-155
[28]   The murine Sim-2 gene product inhibits transcription by active repression and functional interference [J].
Moffett, P ;
Reece, M ;
Pelletier, J .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (09) :4933-4947
[29]  
Mogil Jefrey S., 1996, Physiology and Behavior, V59, P123, DOI 10.1016/0031-9384(95)02073-X
[30]  
OCALLAGHAN JP, 1975, J PHARMACOL EXP THER, V192, P497