| Literature DB >> 31171447 |
Frank Koopmans1, Pim van Nierop2, Maria Andres-Alonso3, Andrea Byrnes4, Tony Cijsouw5, Marcelo P Coba6, L Niels Cornelisse7, Ryan J Farrell8, Hana L Goldschmidt9, Daniel P Howrigan4, Natasha K Hussain10, Cordelia Imig11, Arthur P H de Jong12, Hwajin Jung13, Mahdokht Kohansalnodehi14, Barbara Kramarz15, Noa Lipstein11, Ruth C Lovering15, Harold MacGillavry16, Vittoria Mariano17, Huaiyu Mi18, Momchil Ninov14, David Osumi-Sutherland19, Rainer Pielot20, Karl-Heinz Smalla20, Haiming Tang18, Katherine Tashman4, Ruud F G Toonen7, Chiara Verpelli21, Rita Reig-Viader22, Kyoko Watanabe23, Jan van Weering7, Tilmann Achsel17, Ghazaleh Ashrafi8, Nimra Asi4, Tyler C Brown4, Pietro De Camilli24, Marc Feuermann25, Rebecca E Foulger15, Pascale Gaudet25, Anoushka Joglekar26, Alexandros Kanellopoulos17, Robert Malenka27, Roger A Nicoll28, Camila Pulido8, Jaime de Juan-Sanz8, Morgan Sheng29, Thomas C Südhof30, Hagen U Tilgner26, Claudia Bagni17, Àlex Bayés22, Thomas Biederer5, Nils Brose11, John Jia En Chua31, Daniela C Dieterich20, Eckart D Gundelfinger20, Casper Hoogenraad16, Richard L Huganir10, Reinhard Jahn14, Pascal S Kaeser12, Eunjoon Kim13, Michael R Kreutz3, Peter S McPherson32, Ben M Neale4, Vincent O'Connor33, Danielle Posthuma23, Timothy A Ryan8, Carlo Sala21, Guoping Feng4, Steven E Hyman4, Paul D Thomas18, August B Smit34, Matthijs Verhage35.
Abstract
Synapses are fundamental information-processing units of the brain, and synaptic dysregulation is central to many brain disorders ("synaptopathies"). However, systematic annotation of synaptic genes and ontology of synaptic processes are currently lacking. We established SynGO, an interactive knowledge base that accumulates available research about synapse biology using Gene Ontology (GO) annotations to novel ontology terms: 87 synaptic locations and 179 synaptic processes. SynGO annotations are exclusively based on published, expert-curated evidence. Using 2,922 annotations for 1,112 genes, we show that synaptic genes are exceptionally well conserved and less tolerant to mutations than other genes. Many SynGO terms are significantly overrepresented among gene variations associated with intelligence, educational attainment, ADHD, autism, and bipolar disorder and among de novo variants associated with neurodevelopmental disorders, including schizophrenia. SynGO is a public, universal reference for synapse research and an online analysis platform for interpretation of large-scale -omics data (https://syngoportal.org and http://geneontology.org).Entities:
Keywords: Gene Ontology; enrichment study; gene annotation; gene set analysis; synapse; synaptic plasticity; synaptic proteome network; synaptome; synaptopathies
Mesh:
Year: 2019 PMID: 31171447 PMCID: PMC6764089 DOI: 10.1016/j.neuron.2019.05.002
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173