Phenotypic profiling of mGlu7 knockout mice reveals new implications for neurodevelopmental disorders. (14th April 2020)

• Record Type: Journal Article
• Authors: Fisher, Nicole M.; Gould, Robert W.; Gogliotti, Rocco G.; McDonald, Annalise J.; Badivuku, Hana; Chennareddy, Susmita; Buch, Aditi B.; Moore, Annah M.; Jenkins, Matthew T.; Robb, W. Hudson; Lindsley, Craig W.; Jones, Carrie K.; Conn, P. Jeffrey; Niswender, Colleen M.
• Is Part Of: Genes, brain, and behavior. Volume 19:Number 7(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-04-14
• Subjects: ADHD -- ASD -- autism -- EEG -- epilepsy -- GRM7 -- mGlu7 -- Rett syndrome -- seizures; Behavior genetics -- Periodicals; Neurogenetics -- Periodicals; 616.8
• DOI: 10.1111/gbb.12654
• Languages: English
• ISSNs: 1601-1848

Abstract

Abstract: Neurodevelopmental disorders are characterized by deficits in communication, cognition, attention, social behavior and/or motor control. Previous studies have pointed to the involvement of genes that regulate synaptic structure and function in the pathogenesis of these disorders. One such gene, GRM7, encodes the metabotropic glutamate receptor 7 (mGlu7 ), a G protein‐coupled receptor that regulates presynaptic neurotransmitter release. Mutations and polymorphisms in GRM7 have been associated with neurodevelopmental disorders in clinical populations; however, limited preclinical studies have evaluated mGlu7 in the context of this specific disease class. Here, we show that the absence of mGlu7 in mice is sufficient to alter phenotypes within the domains of social behavior, associative learning, motor function, epilepsy and sleep. Moreover, Grm7 knockout mice exhibit an attenuated response to amphetamine. These findings provide rationale for further investigation of mGlu7 as a potential therapeutic target for neurodevelopmental disorders such as idiopathic autism, attention deficit hyperactivity disorder and Rett syndrome. Abstract : Mice lacking the metabotropic glutamate receptor 7 exhibit a variety of altered phenotypes that have relevance to neurodevelopmental disorders