Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (50)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Chrast, R.
Right arrow Articles by Antonarakis, S. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chrast, R.
Right arrow Articles by Antonarakis, S. E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Molecular Genetics, 2000, Vol. 9, No. 12 1853-1864
© 2000 Oxford University Press

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

Roman Chrast1,2, Hamish S. Scott1, Rime Madani3, Lars Huber3, David P. Wolfer3, Marco Prinz4, Adriano Aguzzi4, Hans-Peter Lipp3 and Stylianos E. Antonarakis,1,+

1Division of Medical Genetics, Geneva University Medical School and University Hospital, 1 Rue Michel-Servet, CH-1211 Genève 4, Switzerland, 2Graduate Program of Cellular and Molecular Biology, Geneva University Medical School, Geneva, Switzerland, 3Institute of Anatomy, University of Zurich, Zurich, Switzerland and 4Institute of Neuropathology, University Hospital of Zurich, Zurich, Switzerland

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.

+ To whom correspondence should be addressed. Tel: +41 22 7025708; Fax: +41 22 7025706; Email: stylianos.antonarakis@medecine.unige.ch


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
N. Ooe, K. Motonaga, K. Kobayashi, K. Saito, and H. Kaneko
Functional Characterization of Basic Helix-Loop-Helix-PAS Type Transcription Factor NXF in Vivo: PUTATIVE INVOLVEMENT IN AN "ON DEMAND" NEUROPROTECTION SYSTEM
J. Biol. Chem., January 9, 2009; 284(2): 1057 - 1063.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
S. Woods, A. Farrall, C. Procko, and M. L. Whitelaw
The bHLH/Per-Arnt-Sim transcription factor SIM2 regulates muscle transcript myomesin2 via a novel, non-canonical E-box sequence
Nucleic Acids Res., June 1, 2008; 36(11): 3716 - 3727.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
B. Laffin, E. Wellberg, H.-I. Kwak, R. C. Burghardt, R. P. Metz, T. Gustafson, P. Schedin, and W. W. Porter
Loss of Singleminded-2s in the Mouse Mammary Gland Induces an Epithelial-Mesenchymal Transition Associated with Up-Regulation of Slug and Matrix Metalloprotease 2
Mol. Cell. Biol., March 15, 2008; 28(6): 1936 - 1946.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
H.-I. Kwak, T. Gustafson, R. P. Metz, B. Laffin, P. Schedin, and W. W. Porter
Inhibition of breast cancer growth and invasion by single-minded 2s
Carcinogenesis, February 1, 2007; 28(2): 259 - 266.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
A. O'Doherty, S. Ruf, C. Mulligan, V. Hildreth, M. L. Errington, S. Cooke, A. Sesay, S. Modino, L. Vanes, D. Hernandez, et al.
An Aneuploid Mouse Strain Carrying Human Chromosome 21 with Down Syndrome Phenotypes
Science, September 23, 2005; 309(5743): 2033 - 2037.
[Abstract] [Full Text] [PDF]


Home page
Mol. Endocrinol.Home page
E. Goshu, H. Jin, J. Lovejoy, J.-F. Marion, J. L. Michaud, and C.-M. Fan
Sim2 Contributes to Neuroendocrine Hormone Gene Expression in the Anterior Hypothalamus
Mol. Endocrinol., May 1, 2004; 18(5): 1251 - 1262.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
N. Ooe, K. Saito, N. Mikami, I. Nakatuka, and H. Kaneko
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
Mol. Cell. Biol., January 15, 2004; 24(2): 608 - 616.
[Abstract] [Full Text] [PDF]


Home page
J. Med. Genet.Home page
D Kamnasaran, W J Muir, M A Ferguson-Smith, and D W Cox
Disruption of the neuronal PAS3 gene in a family affected with schizophrenia
J. Med. Genet., May 1, 2003; 40(5): 325 - 332.
[Abstract] [Full Text] [PDF]


Home page
Cold Spring Harb Symp Quant BiolHome page
A.G. CLARK, S. GLANOWSKI, R. NIELSEN, P. THOMAS, A. KEJARIWAL, M.J. TODD, D.M. TANENBAUM, D. CIVELLO, F. LU, B. MURPHY, et al.
Positive Selection in the Human Genome Inferred from Human-Chimp-Mouse Orthologous Gene Alignments
Cold Spring Harb Symp Quant Biol, January 1, 2003; 68(0): 479 - 486.
[Abstract] [PDF]


Home page
Mol. Cell. Biol.Home page
E. Goshu, H. Jin, R. Fasnacht, M. Sepenski, J. L. Michaud, and C.-M. Fan
Sim2 Mutants Have Developmental Defects Not Overlapping with Those of Sim1 Mutants
Mol. Cell. Biol., June 15, 2002; 22(12): 4147 - 4157.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. L. Woods and M. L. Whitelaw
Differential Activities of Murine Single Minded 1 (SIM1) and SIM2 on a Hypoxic Response Element. CROSS-TALK BETWEEN BASIC HELIX-LOOP-HELIX/Per-Arnt-Sim HOMOLOGY TRANSCRIPTION FACTORS
J. Biol. Chem., March 15, 2002; 277(12): 10236 - 10243.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
M. D. Lalioti and J. K. Heath
A new method for generating point mutations in bacterial artificial chromosomes by homologous recombination in Escherichia coli
Nucleic Acids Res., February 1, 2001; 29(3): e14 - e14.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.