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.
引用
收藏
页码:1853 / 1864
页数:12
相关论文
共 39 条
[1]   10 years of genomics, chromosome 21, and Down syndrome [J].
Antonarakis, SE .
GENOMICS, 1998, 51 (01) :1-16
[2]   DOWNS-SYNDROME - ABNORMAL NEUROMUSCULAR-JUNCTION IN TONGUE OF TRANSGENIC MICE WITH ELEVATED LEVELS OF HUMAN CU/ZN-SUPEROXIDE DISMUTASE [J].
AVRAHAM, KB ;
SCHICKLER, M ;
SAPOZNIKOV, D ;
YAROM, R ;
GRONER, Y .
CELL, 1988, 54 (06) :823-829
[3]   Deletion of the ryanodine receptor type 3 (RyR3) impairs forms of synaptic plasticity and spatial learning [J].
Balschun, D ;
Wolfer, DP ;
Bertocchini, F ;
Barone, V ;
Conti, A ;
Zuschratter, W ;
Missiaen, L ;
Lipp, HP ;
Frey, JU ;
Sorrentino, V .
EMBO JOURNAL, 1999, 18 (19) :5264-5273
[4]   SINGLE-MINDED AND DOWN-SYNDROME [J].
CHEN, H ;
CHRAST, R ;
ROSSIER, C ;
GOS, A ;
ANTONARAKIS, SE ;
KUDOH, J ;
YAMAKI, A ;
SHINDOH, N ;
MAEDA, H ;
MINOSHIMA, S ;
SHIMIZU, N .
NATURE GENETICS, 1995, 10 (01) :9-10
[5]   Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping [J].
Chen, H ;
Chrast, R ;
Rossier, C ;
Morris, MA ;
Lalioti, MD ;
Antonarakis, SE .
GENOME RESEARCH, 1996, 6 (08) :747-760
[6]   Cloning of two human homologs of the Drosophila single-minded gene SIM1 on chromosome 6q and SIM2 on 21q within the down syndrome chromosomal region [J].
Chrast, R ;
Scott, HS ;
Chen, HM ;
Kudoh, J ;
Rossier, C ;
Minoshima, S ;
Wang, YM ;
Shimizu, N ;
Antonarakis, SE .
GENOME RESEARCH, 1997, 7 (06) :615-624
[7]   Linearization and purification of BAC DNA for the development of transgenic mice [J].
Chrast, R ;
Scott, HS ;
Antonarakis, SE .
TRANSGENIC RESEARCH, 1999, 8 (02) :147-150
[8]   THE DROSOPHILA SINGLE-MINDED GENE ENCODES A NUCLEAR-PROTEIN WITH SEQUENCE SIMILARITY TO THE PER GENE-PRODUCT [J].
CREWS, ST ;
THOMAS, JB ;
GOODMAN, CS .
CELL, 1988, 52 (01) :143-151
[9]   Control of cell lineage-specific development and transcription by bHLH-PAS proteins [J].
Crews, ST .
GENES & DEVELOPMENT, 1998, 12 (05) :607-620
[10]  
Delabar Jean-Maurice, 1993, European Journal of Human Genetics, V1, P114