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U.S. Department of Health and Human Services NATIONAL INSTITUTES OF HEALTH NIH News National Human Genome Research Institute (NHGRI)<http://www.genome.nih.gov/> For Immediate Release: Tuesday, March 14, 2023 CONTACT: Mauresa Pittman, 301-402-0911,<email:mauresa.pittman@xxxxxxx>
RESEARCHERS STUDY ENHANCED GENETIC ANIMAL MODEL OF DOWN SYNDROME New mouse model may inform potential therapeutic options for Down syndrome
National Institutes of Health researchers compared a new genetic animal model of Down syndrome to the standard model and found the updated version to be more similar to the changes seen in humans. The new mouse model shows milder cognitive
traits compared to a previously studied Down syndrome mouse model. The results of this study, published in Biological Psychiatry, may help researchers develop more precise treatments to improve learning and memory in people with Down syndrome. Scientists found that the new mouse model, known as Ts66Yah, had memory difficulties and behavior traits, but the symptoms were not as severe as seen with the previous mouse model. Scientists often use different strains of mice as animal
models <https://www.genome.gov/genetics-glossary/Mouse-Model> to study human diseases because most genes in humans have similar counterparts in mice.
“A mouse model that more precisely captures the genetics of Down syndrome has important implications for human clinical trials that aim to improve cognition,” said Diana W. Bianchi, M.D., director of the Eunice Kennedy Shriver National
Institute of Child Health and Human Development, senior investigator in the National Human Genome Research Institute (NHGRI) Center for Precision Health Research and senior author of the study. About 6,000 newborns are diagnosed with Down syndrome < https://www.genome.gov/genetics-glossary/Down-Syndrome-Trisomy-21>each year in the United States. In most cases, these babies have a third copy of chromosome 21. An additional chromosome
21 adds an extra copy of over 200 protein-coding genes to that person’s genome, which causes difficulties with learning, speech and motor skills. A previous mouse model, known as Ts65Dn, has been considered the standard for Down syndrome research, used in preclinical studies for nearly 30 years. Along with some successful cognitive treatments, such as a recent hormone-based cognitive
treatment <https://www.science.org/doi/10.1126/science.abq4515>, some other treatments that were effective in the mouse model were not as effective in humans. Importantly, the previous mouse model’s genome contains 45 extra genes that are irrelevant to human Down syndrome, a byproduct of how the model was developed. Humans and mice have very similar genomes, but the chromosomes that make up those
genomes do not precisely align across those two species. For example, many of the genes found on human chromosome 21 are found on mouse chromosomes 16 and 17. The previous mouse model has an additional region of mouse chromosome 17 that contains 45 extra genes
not found on human chromosome 21. How these 45 extra genes affect the brain and behavior of the previous Ts65Dn mice has not been investigated until now. To create an enhanced mouse model of Down syndrome, researchers at the University of Strasbourg, France, removed these extra 45 genes using CRISPR gene-editing technology. Dr. Bianchi’s group then compared the two mouse models and found
that the extra 45 genes in the previous mouse model were affecting brain development and contributed to more severe difficulties with motor skills, communication and memory. “There are considerable effects of these extra genes on mouse brain development and behavior,” said Faycal Guedj, Ph.D., staff scientist in NHGRI's Center for Precision Health Research and first author of the study. “What was previously
thought as the best mouse model of Down syndrome has traits derived from genes that are not relevant to human chromosome 21.” Researchers at the Center for Precision Health Research < https://www.genome.gov/about-nhgri/Division-of-Intramural-Research/Center-for-Precision-Health-Research> aim to use cutting-edge genomics tools to foster next-generation healthcare.
With this new and improved mouse model, Dr. Bianchi’s group hopes to develop more precise treatments for improving cognition with the goal of independent living skills in people with Down syndrome.
"The possibility of treating intellectual disabilities in the context of Down syndrome goes to the core of changing conceptions about the nature of disability, its medical and clinical aspects, and what we, often pejoratively, consider
‘normal’ and ‘desirable’ in the context of medical care and in society,” underscores Christopher R. Donohue, Ph.D., NHGRI senior historian. “As cognitive treatments based on genetic models become more feasible in the future, researchers, in conversation with
disability ethicists, those with Down syndrome and other healthcare professionals, should carefully weigh potential benefits versus drawbacks, including contributing to ableism in medicine, and other forms of stigma.”
The National Human Genome Research Institute (NHGRI) is one of the 27 institutes and centers at the NIH, an agency of the Department of Health and Human Services. The NHGRI Division of Intramural Research develops and implements technology
to understand, diagnose and treat genomic and genetic diseases. Additional information about NHGRI can be found at: <https://www.genome.gov/>. About the National Institutes of Health (NIH): NIH, the nation's medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting
and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit <https://www.nih.gov>. NIH...Turning Discovery into Health -- Registered, U.S. Patent and Trademark Office ### To subscribe (or unsubscribe) from NIH News Release mailings, go to <http://service.govdelivery.com/service/subscribe.html?code=USNIH_1>. If you subscribed via the NIH LISTSERV, go to <https://list.nih.gov/cgi-bin/wa.exe?A0=nihpress>. |
