15/05/2017
Epilepsy and Intellectual Disability, which usually have their onset during childhood, are in some cases linked to mutations in the gene KIAA1202, which contains the information to produce the protein Shrm4. An international study, published on Nature Communication, coordinated by Maria Passafaro, at the Institute of Neuroscience of the National Research Council (IN-CNR), demonstrated one possible mechanism by which these mutations could cause those pathologies.
“Research community has been always interested in understanding the link between different mutations and the onset of these pathologies and recent studies have shown a direct relation between mutations on the KIA1202 gene and the insurgence of these diseases in some families” Passafaro states. “Our work provides a step further for the knowledge of these disorders, unravelling the role of Shrm4 protein. This protein is crucial since it is responsible of the correct positioning of GABAB receptors. We observed that this activity occurs through the molecular motor Dynein, and that Shrm4 acts as an adaptor between the motor and GABAB receptors, thus allowing its correct localization in synapses (the contact points that allow the communication between neurons and with other cells). What we found is that, when Shrm4 is absent, GABAB receptors cannot reach synapses and thus cannot exert their function”.
The researchers registered electric currents in the hippocampus of animals deprived of Shrm4, and found a reduction of the inhibitory component. “The consequence of this is an increase in epileptic seizures in these animals, together with other defects such as increased anxious behaviours, impairments in learning and sociability. From these results we can start to hypothesize new treatments for patients that harbour these mutations” Passafaro concludes.
Who: IN-CNR, Milan
What: A new molecular mechanism by which mutations in the KIA1202 gene lead to epilepsy and intellectual disability. Published on Nature Communication 'Epilepsy and intellectual disability linked protein Shrm4 interaction with GABABRs shapes inhibitory neurotransmission'; Jonathan Zapata, Edoardo Moretto Saad Hannan, Luca Murru, Anna Longatti, Davide Mazza, Lorena Benedetti, Matteo Fossati, Christopher Heise, Luisa Ponzoni, Pamela Valnegri, Daniela Braida, Mariaelvina Sala, Maura Francolini, Jeffrey Hildebrand, Vera Kalscheuer, Francesca Fanelli, Carlo Sala, Bernhard Bettler, Silvia Bassani, Trevor G. Smart & Maria Passafaro
https://www.nature.com/articles/ncomms14536
Per informazioni:
Edoardo Moretto
In-Cnr
e.moretto@in.cnr.it
02/50317102
Ufficio stampa:
Cecilia Migali
cecilia.migali@cnr.it
06/49933216
Responsabile Unità Ufficio stampa:
Marco Ferrazzoli
marco.ferrazzoli@cnr.it
ufficiostampa@cnr.it
06 4993 3383