Rodent models in Down syndrome research: impact and future opportunities

Author:

Herault Yann12345ORCID,Delabar Jean M.5678ORCID,Fisher Elizabeth M. C.5910ORCID,Tybulewicz Victor L. J.5101112ORCID,Yu Eugene51314ORCID,Brault Veronique1234ORCID

Affiliation:

1. Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, 1 rue Laurent Fries, 67404 Illkirch, France

2. Centre National de la Recherche Scientifique, UMR7104, Illkirch, France

3. Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, France

4. Université de Strasbourg, 67404 Illkirch, France

5. T21 Research Society, Brain and Spine Institute (ICM), 75013 Paris

6. Université Paris Diderot, Sorbonne Paris Cité, Unité de Biologie Fonctionnelle et Adaptative, UMR8251, CNRS, 75205 Paris, France

7. INSERM U 1127, CNRS UMR 7225, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, Institut du Cerveau et la Moelle épinière, ICM, 75013 Paris, France

8. Brain and Spine Institute (ICM) CNRS UMR7225, INSERM UMRS 975, 75013 Paris, France

9. Department of Neurodegenerative Disease, Institute of Neurology, University College London, London, WC1N 3BG, UK

10. LonDownS Consortium, London, W1T 7NF UK

11. The Francis Crick Institute, 1 Midland Road, London, NW1 1AT, UK

12. Department of Medicine, Imperial College, London, SW7 2AZ, UK

13. The Children's Guild Foundation Down Syndrome Research Program, Department of Cancer Genetics and Genetics Program, Roswell Park Cancer Institute, Buffalo, NY 14263, USA

14. Department of Cellular and Molecular Biology, Roswell Park Division of Graduate School, Genetics, Genomics and Bioinformatics Program, State University of New York at Buffalo, Buffalo, NY 14263, USA

Abstract

ABSTRACT Down syndrome is caused by trisomy of chromosome 21. To date, a multiplicity of mouse models with Down-syndrome-related features has been developed to understand this complex human chromosomal disorder. These mouse models have been important for determining genotype-phenotype relationships and identification of dosage-sensitive genes involved in the pathophysiology of the condition, and in exploring the impact of the additional chromosome on the whole genome. Mouse models of Down syndrome have also been used to test therapeutic strategies. Here, we provide an overview of research in the last 15 years dedicated to the development and application of rodent models for Down syndrome. We also speculate on possible and probable future directions of research in this fast-moving field. As our understanding of the syndrome improves and genome engineering technologies evolve, it is necessary to coordinate efforts to make all Down syndrome models available to the community, to test therapeutics in models that replicate the whole trisomy and design new animal models to promote further discovery of potential therapeutic targets.

Funder

Centre National de la Recherche Scientifique

Institut National de la Santé et de la Recherche Médicale

Université de Strasbourg

European Commission

Fifth Framework Programme

Agence Nationale de la Recherche

Sixth Framework Programme

Wellcome Trust

Francis Crick Institute

National Institutes of Health

Roswell Park Alliance Foundation, Roswell Park Cancer Institute

Fondation Jérôme Lejeune

Publisher

The Company of Biologists

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology and Microbiology (miscellaneous),Medicine (miscellaneous),Neuroscience (miscellaneous)

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