Editorial: Shankopathies: Shank Protein Deficiency-Induced Synaptic Diseases

Human Genetics and Cognitive Functions, Institut Pasteur, UMR 3571 CNRS, Université de Paris, Paris, France, 2 Institute for Anatomy and Cell Biology, Ulm University, Ulm, Germany, Center for Synaptic Brain Dysfunctions, Institute for Basic Science, Daejeon, South Korea, Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, South Korea, Department of Neuroscience, and Biomedical Sciences, Korea University College of Medicine,


Shankopathies: Shank Protein Deficiency-Induced Synaptic Diseases
SHANK (also known as ProSAP) proteins are postsynaptic core scaffolds involved in excitatory synapse development, function, and plasticity. The three members of the SHANK family (SHANK1, SHANK2, and SHANK3) differ in their temporal and regional expression patterns in the central nervous system and non-neuronal tissue during development. Mutations in the cognate genes are associated with various neuropsychiatric conditions, such as autism spectrum disorders, Phelan-McDermid syndrome, intellectual disability, schizophrenia, and bipolar disorder. Exactly how defects in SHANK proteins contribute to these conditions is currently under active investigation.
The present Research Topic provides an overview of current knowledge on the involvement of SHANK genes in neuropsychiatric disorders. Shankopathies are explored at different scales: genes, proteins, cells, synapses, neural circuits, behaviors, and environment. For example, Eltokhi et al. observed that the large phenotypic diversity of patients carrying SHANK2 mutations is reflected in the phenotypic diversity displayed by the various Shank2 mouse models. Hassani Nia and Kreienkamp reviewed the effects of Shank3 mutations on the gene, protein, and synaptic signaling. Both reviews provide a comprehensive state-of-the-art overview on SHANK2 and SHANK3 different scales. An example of how mouse models can closely mimic human Shankopathies was provided by the comprehensive characterization of the Shank3 Q321R knock-in model conducted by Yoo et al..
The other contributions address two major questions for Shankopathies: (i) Are there specific modulating factors for Shankopathies and (ii) Which brain regions are specifically affected by Shankopathies?
Concerning the first question, three putative modulating factors were examined; namely, pharmacological intervention (pharmacological modulation of phenotypes), sexual hormones, and zinc. Sungur et al. explored whether Shank1 mutant mice and control mice were equally sensitive to amphetamine and methylenedioxymethamphetamine. In Shank2 mutant mice, Ey et al. demonstrated that the abnormal social behavior of Shank2 knockout mice was associated with a deficit in social motivation, but with an intact social recognition phenotype. They also highlighted that methylphenidate is ineffective in restoring typical activity levels in hyperactive Shank2 knockout mice. By contrast, Berkel et al. examined the role of an inherent modulating factor; namely, sexual hormones, on Shank1, Shank2, and Shank3 gene transcription and protein levels. The role of sexual hormones as transcriptional finetuners, especially shortly before or after birth, might explain sex-related differences in patients and animal models. Finally, zinc was identified as a potentially major modulating factor in Shankopathies, given its role in recruiting Shank2 and Shank3 at synapses, as well as having a key role in the gastro-intestinal tract, as reviewed by Hagmeyer et al.. At the molecular level, the mode of regulation of AMPA receptor (AMPAR) subunit composition by Shank2, Shank3 and zinc was explored by Ha et al.. Zinc regulated the switch during development of AMPARs lacking GluA2 to AMPARs containing GluA2, while Shank2 and Shank3 also regulated this process. At the scale of the organism, Fourie et al. tested the effect of long-term zinc supplementation in alimentation of the Shank3 ex13−16 mouse model. Importantly, some aspects of synaptic transmission and some behavioral traits, such as self-grooming, were rescued. Taken together, the studies on zinc presented in this Research Topic present evidence that zinc is a promising potential new therapeutic agent for Shankopathies.
Regarding the second question on brain regions specifically affected by Shankopathies, different approaches were used to investigate the effect of Shank mutations at the different scales of observation. Yoo et al. highlighted that a conditional Shank3 knockout (targeting exons 14-16, encoding the PDZ domain) in GABAergic neurons (enriched in the striatum) induces a strong reduction of excitatory synaptic inputs onto dorsal striatal neurons as observed in global Shank3 ex14−16 mutant mice. However, the conditional knockout leads to milder social deficits and stereotyped behaviors than global Shank3 ex14−16 mutant mice. Using magnetic resonance imaging (MRI), Schoen et al. examined mouse brain anatomy during development showing that total brain volume, cerebellar volume, and cortical thickness were unaffected in homozygous and heterozygous Shank3 mutant mice and the prenatal zinc deficiency model compared to wild-type controls. By contrast, the striatal volume and the globus pallidus volume were increased in both models, while the changes in the thalamus were reduced in the Shank3 mouse model and increased in the prenatal zinc deficiency mouse model. Transcriptomic analyses allowed (Jin et al.) to identify brain region-specific modulation of gene expression in different Shank3 models, across age classes and between brain regions (prefrontal cortex, striatum, and hippocampus). This analysis highlighted an important modulation of the expression of myelin-related and ribosome-related genes. At the protein level, Heise et al. found that Shank2 and Shank3 mutant mice displayed a reduced expression of receptors specific to excitatory synaptic transmission in the striatum and in the thalamus (for Shank2 also in the cortex and cerebellum). These models were compared to another mouse model of neurodevelopmental disorders, the Cntn4 mutant that displays increased surface expression of glutamatergic receptors (GluA1 and GluA2) in the striatum or downregulation of GABAergic receptors (GABAA) in several brain regions. Finally, the involvement of the reward system was examined directly and indirectly. In the direct approach, Bariselli et al. knocked down Shank3 in the ventral tegmental area in mice and observed a dysfunction in social-seeking behavior. The indirect approach concerned the characterization of a Shank2 model in another species, namely the Shank2 ex31 mutant rat, characterized by Modi et al.. Shank2 ex31 mutant rats displayed an atypically high motivation to collect food reward, in parallel with social deficits, impaired learning, increased activity, and repetitive circling, combined with increased striatal activity and decreased hippocampal function.
In summary, this Research Topic provided a multi-scale overview of the current state of knowledge on Shankopathies. The research studies contribute to the understanding of the spectrum of disorders related to SHANK mutations, as well as providing prospects for new potential therapeutic strategies, targeting specific brain regions or modulating factors.