Public Release: 

Mouse model of intellectual disability isolates learning gene

A new way to study learning and memory, intellectual disability

Society for Neuroscience

IMAGE

IMAGE: CrbnKO mice show altered mTORC1 signaling in the hippocampus. Schematic of proposed molecular mechanism. view more 

Credit: Bavley et al., JNeurosci (2018)

Adult male mice lacking a gene linked to intellectual disability have trouble completing and remembering mazes, with no changes in social or repetitive behavior, according to new research published in JNeurosci. This animal model provides a new way to study the role of this gene in learning and memory and provides a rodent model of pure intellectual disability.

A mutation in the gene CRBN causes a type of intellectual disability in humans that is defined by a low intelligence quotient. Intellectual disability has been studied in the context of complex disorders like autism spectrum disorder, Fragile X and Down syndrome that co-occur with other conditions, which has made it difficult to selectively understand cognitive impairment.

Anjali Rajadhyaksha, director of the Weill Cornell Autism Research Program, associate professor of neuroscience in pediatrics and of neuroscience at the Feil Family Brain and Mind Research Institute at Weill Cornell Medicine, and colleagues deleted the mouse Crbn gene and demonstrated that these mice, compared to mice with the intact gene, have difficulty navigating mazes designed to test learning and memory abilities, dependent on the hippocampus. Treating the mice with a compound that inhibits the activity of an enzyme in the hippocampus improved the learning and memory deficits. The researchers did not observe any differences in the preference of altered mice to interact with a fellow mouse or in repetitive grooming behavior, indicating that the gene is not associated with behaviors that often co-occur with intellectual disability, as in autism.

###

Article: Rescue of learning and memory deficits in the human non-syndromic intellectual disability cereblon knockout mouse model by targeting the AMPK-mTORC1 translational pathway

DOI: https://doi.org/10.1523/JNEUROSCI.0599-17.2018

Corresponding author:

Anjali Rajadhyaksha
Weill Cornell Medicine, New York, NY, USA
amr2011@med.cornell.edu

About JNeurosci

JNeurosci, the Society for Neuroscience's first journal, was launched in 1981 as a means to communicate the findings of the highest quality neuroscience research to the growing field. Today the journal remains committed to publishing cutting-edge neuroscience that will have an immediate and lasting scientific impact while responding to authors' changing publishing needs, representing breadth of the field and diversity in authorship.

About The Society for Neuroscience

The Society for Neuroscience is the world's largest organization of scientists and physicians devoted to understanding the brain and nervous system. The nonprofit organization, founded in 1969, now has nearly 37,000 members in more than 90 countries and over 130 chapters worldwide.

Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.