PRRT2, a network stability gene

Specific paroxysmal disorders, namely benign infantile epilepsy (BFIE), kinesigenic dyskinesia (PKD), infantile convulsions and choreoathetosis (ICCA) and hemiplegic migraine (HM), are associated with mutations in the gene encoding for PRoline-Rich Transmembrane protein 2 (PRRT2; Figure 1A, 1B). PRRT2 is a neuronspecific protein expressed on neuronal membranes and at synapses, with a prevalent presynaptic location [1, 2]. Several nonsense, missense and frame-shift mutations were identified in the PRRT2 gene, but the vast majority of patients (80%) carry the same frameshift single-nucleotide duplication (c.649dupC) that leads to a premature stop codon and results in a loss-of-function pathogenetic mechanism [3]. Despite the extensive characterization of PRRT2 mutations, no clear evidence for genotypephenotype correlation exists and the three main diseases (BFIE, PKD and PKD/ICCA) form a continuous spectrum, starting from BFIE in the first months of life and evolving to PKD or PKD/ICCA often in association with HM during adolescence [4-5]. To model the disorders and investigate the underlying neurobiological alterations, we recently characterized a PRRT2 knock out mouse (PRRT2 KO; Figure 1C), carrying a constitutive inactivation of the PRRT2 gene [6]. The promoterless lacZ gene integrated into the PRRT2 locus allowed mapping the PRRT2 regional expression, that is not widespread, but rather concentrated at restricted brain areas. Interestingly, the expression is high in neurons of the lower hindbrain particularly in the cerebellum, a brain area involved in the generation of motor/epileptic phenotype and in which altered synaptic plasticity at the parallel fibersPurkinje cells synapse was found [6] (Figure 1D). A selective staining was also identified in the cerebral cortex, claustrum and dorsal horns of the spinal cord. Moreover, in the hippocampus, PRRT2 is particularly expressed in the hilus of the dentate gyrus, where mossy cells control the excitability of granule cells, playing a role in preventing hippocampal seizures (Figure 1D). Notably, all the brain regions positive for PRRT2 are involved in processing sensory information, motor disorders and epilepsy, all neurological traits present in patients with PRRT2 mutations. The PRRT2 KO mouse recapitulates many of the phenotypic features of the human PRRT2-linked disorders, showing abnormal motor behaviors and a motor/epileptic phenotype in response to environmental stimuli [6]. The motor problems are represented by gait abnormalities and a peculiar paroxysmal backwalking appearing early in the postnatal life and persisting in the adult [4]. The motor/ epileptic phenotype of PRRT2 KO mice becomes dramatic in response to audiogenic stimuli (Figure 1E), which trigger wild running, backwalking and jumping, and to the administration of convulsants, such as pentylentetrazole (Figure 1F). In both kinds of provocations, however, the seizure propensity was not very severe, consistent with the mild epileptic phenotype of patients bearing PRRT2 mutations [4, 5]. Overall, the PRRT2 KO mouse reproduces the paroxysmal traits described in PRRT2 patients and characterized by sudden and short attacks that usually occur periodically in response to a sensory trigger. The episodic nature of these events suggests that they result from network instability caused by changes in the excitation/inhibition balance. Interestingly, data obtained in primary neurons showed that PRRT2 silencing is associated with alterations of synaptic transmission and short-term plasticity [1]. PRRT2 silencing gives rise to a decreased number of excitatory synapses and a marked impairment of fast synchronous neurotransmitter release. These effects are associated with a decrease in Ca2+ sensitivity and release probability, revealing a role for Editorial