Literature DB >> 24179158

The human language-associated gene SRPX2 regulates synapse formation and vocalization in mice.

G M Sia1, R L Clem, R L Huganir.   

Abstract

Synapse formation in the developing brain depends on the coordinated activity of synaptogenic proteins, some of which have been implicated in a number of neurodevelopmental disorders. Here, we show that the sushi repeat-containing protein X-linked 2 (SRPX2) gene encodes a protein that promotes synaptogenesis in the cerebral cortex. In humans, SRPX2 is an epilepsy- and language-associated gene that is a target of the foxhead box protein P2 (FoxP2) transcription factor. We also show that FoxP2 modulates synapse formation through regulating SRPX2 levels and that SRPX2 reduction impairs development of ultrasonic vocalization in mice. Our results suggest FoxP2 modulates the development of neural circuits through regulating synaptogenesis and that SRPX2 is a synaptogenic factor that plays a role in the pathogenesis of language disorders.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 24179158      PMCID: PMC3903157          DOI: 10.1126/science.1245079

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  32 in total

Review 1.  Structure and flexibility of the multiple domain proteins that regulate complement activation.

Authors:  M D Kirkitadze; P N Barlow
Journal:  Immunol Rev       Date:  2001-04       Impact factor: 12.988

2.  SRPX2 mutations in disorders of language cortex and cognition.

Authors:  Patrice Roll; Gabrielle Rudolf; Sandrine Pereira; Barbara Royer; Ingrid E Scheffer; Annick Massacrier; Maria-Paola Valenti; Nathalie Roeckel-Trevisiol; Sarah Jamali; Christophe Beclin; Caroline Seegmuller; Marie-Noëlle Metz-Lutz; Arnaud Lemainque; Marc Delepine; Christophe Caloustian; Anne de Saint Martin; Nadine Bruneau; Danièle Depétris; Marie-Geneviève Mattéi; Elisabeth Flori; Andrée Robaglia-Schlupp; Nicolas Lévy; Bernd A Neubauer; Rivka Ravid; Christian Marescaux; Samuel F Berkovic; Edouard Hirsch; Mark Lathrop; Pierre Cau; Pierre Szepetowski
Journal:  Hum Mol Genet       Date:  2006-02-23       Impact factor: 6.150

3.  hikaru genki, a CNS-specific gene identified by abnormal locomotion in Drosophila, encodes a novel type of protein.

Authors:  M Hoshino; F Matsuzaki; Y Nabeshima; C Hama
Journal:  Neuron       Date:  1993-03       Impact factor: 17.173

4.  Humanized Foxp2 specifically affects cortico-basal ganglia circuits.

Authors:  S Reimers-Kipping; W Hevers; S Pääbo; W Enard
Journal:  Neuroscience       Date:  2010-11-25       Impact factor: 3.590

5.  Activity-dependent regulation of inhibitory synapse development by Npas4.

Authors:  Yingxi Lin; Brenda L Bloodgood; Jessica L Hauser; Ariya D Lapan; Alex C Koon; Tae-Kyung Kim; Linda S Hu; Athar N Malik; Michael E Greenberg
Journal:  Nature       Date:  2008-09-24       Impact factor: 49.962

6.  Activity-dependent regulation of MEF2 transcription factors suppresses excitatory synapse number.

Authors:  Steven W Flavell; Christopher W Cowan; Tae-Kyung Kim; Paul L Greer; Yingxi Lin; Suzanne Paradis; Eric C Griffith; Linda S Hu; Chinfei Chen; Michael E Greenberg
Journal:  Science       Date:  2006-02-17       Impact factor: 47.728

Review 7.  Mouse behavioral assays relevant to the symptoms of autism.

Authors:  Jacqueline N Crawley
Journal:  Brain Pathol       Date:  2007-10       Impact factor: 6.508

8.  LRRTM2 interacts with Neurexin1 and regulates excitatory synapse formation.

Authors:  Joris de Wit; Emily Sylwestrak; Matthew L O'Sullivan; Stefanie Otto; Katie Tiglio; Jeffrey N Savas; John R Yates; Davide Comoletti; Palmer Taylor; Anirvan Ghosh
Journal:  Neuron       Date:  2009-12-24       Impact factor: 17.173

9.  The classical complement cascade mediates CNS synapse elimination.

Authors:  Beth Stevens; Nicola J Allen; Luis E Vazquez; Gareth R Howell; Karen S Christopherson; Navid Nouri; Kristina D Micheva; Adrienne K Mehalow; Andrew D Huberman; Benjamin Stafford; Alexander Sher; Alan M Litke; John D Lambris; Stephen J Smith; Simon W M John; Ben A Barres
Journal:  Cell       Date:  2007-12-14       Impact factor: 41.582

10.  Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

Authors:  Peter Szatmari; Andrew D Paterson; Lonnie Zwaigenbaum; Wendy Roberts; Jessica Brian; Xiao-Qing Liu; John B Vincent; Jennifer L Skaug; Ann P Thompson; Lili Senman; Lars Feuk; Cheng Qian; Susan E Bryson; Marshall B Jones; Christian R Marshall; Stephen W Scherer; Veronica J Vieland; Christopher Bartlett; La Vonne Mangin; Rhinda Goedken; Alberto Segre; Margaret A Pericak-Vance; Michael L Cuccaro; John R Gilbert; Harry H Wright; Ruth K Abramson; Catalina Betancur; Thomas Bourgeron; Christopher Gillberg; Marion Leboyer; Joseph D Buxbaum; Kenneth L Davis; Eric Hollander; Jeremy M Silverman; Joachim Hallmayer; Linda Lotspeich; James S Sutcliffe; Jonathan L Haines; Susan E Folstein; Joseph Piven; Thomas H Wassink; Val Sheffield; Daniel H Geschwind; Maja Bucan; W Ted Brown; Rita M Cantor; John N Constantino; T Conrad Gilliam; Martha Herbert; Clara Lajonchere; David H Ledbetter; Christa Lese-Martin; Janet Miller; Stan Nelson; Carol A Samango-Sprouse; Sarah Spence; Matthew State; Rudolph E Tanzi; Hilary Coon; Geraldine Dawson; Bernie Devlin; Annette Estes; Pamela Flodman; Lambertus Klei; William M McMahon; Nancy Minshew; Jeff Munson; Elena Korvatska; Patricia M Rodier; Gerard D Schellenberg; Moyra Smith; M Anne Spence; Chris Stodgell; Ping Guo Tepper; Ellen M Wijsman; Chang-En Yu; Bernadette Rogé; Carine Mantoulan; Kerstin Wittemeyer; Annemarie Poustka; Bärbel Felder; Sabine M Klauck; Claudia Schuster; Fritz Poustka; Sven Bölte; Sabine Feineis-Matthews; Evelyn Herbrecht; Gabi Schmötzer; John Tsiantis; Katerina Papanikolaou; Elena Maestrini; Elena Bacchelli; Francesca Blasi; Simona Carone; Claudio Toma; Herman Van Engeland; Maretha de Jonge; Chantal Kemner; Frederieke Koop; Frederike Koop; Marjolein Langemeijer; Marjolijn Langemeijer; Channa Hijmans; Channa Hijimans; Wouter G Staal; Gillian Baird; Patrick F Bolton; Michael L Rutter; Emma Weisblatt; Jonathan Green; Catherine Aldred; Julie-Anne Wilkinson; Andrew Pickles; Ann Le Couteur; Tom Berney; Helen McConachie; Anthony J Bailey; Kostas Francis; Gemma Honeyman; Aislinn Hutchinson; Jeremy R Parr; Simon Wallace; Anthony P Monaco; Gabrielle Barnby; Kazuhiro Kobayashi; Janine A Lamb; Ines Sousa; Nuala Sykes; Edwin H Cook; Stephen J Guter; Bennett L Leventhal; Jeff Salt; Catherine Lord; Christina Corsello; Vanessa Hus; Daniel E Weeks; Fred Volkmar; Maïté Tauber; Eric Fombonne; Andy Shih; Kacie J Meyer
Journal:  Nat Genet       Date:  2007-02-18       Impact factor: 38.330

View more
  53 in total

1.  Deletion of Autism Risk Gene Shank3 Disrupts Prefrontal Connectivity.

Authors:  Marco Pagani; Alice Bertero; Adam Liska; Alberto Galbusera; Mara Sabbioni; Noemi Barsotti; Nigel Colenbier; Daniele Marinazzo; Maria Luisa Scattoni; Massimo Pasqualetti; Alessandro Gozzi
Journal:  J Neurosci       Date:  2019-05-06       Impact factor: 6.167

2.  Kctd13 deletion reduces synaptic transmission via increased RhoA.

Authors:  Christine Ochoa Escamilla; Irina Filonova; Angela K Walker; Zhong X Xuan; Roopashri Holehonnur; Felipe Espinosa; Shunan Liu; Summer B Thyme; Isabel A López-García; Dorian B Mendoza; Noriyoshi Usui; Jacob Ellegood; Amelia J Eisch; Genevieve Konopka; Jason P Lerch; Alexander F Schier; Haley E Speed; Craig M Powell
Journal:  Nature       Date:  2017-11-01       Impact factor: 49.962

3.  Differential FoxP2 and FoxP1 expression in a vocal learning nucleus of the developing budgerigar.

Authors:  Osceola Whitney; Tawni Voyles; Erina Hara; Qianqian Chen; Stephanie A White; Timothy F Wright
Journal:  Dev Neurobiol       Date:  2014-11-26       Impact factor: 3.964

4.  Inter-tissue coexpression network analysis reveals DPP4 as an important gene in heart to blood communication.

Authors:  Quan Long; Carmen Argmann; Sander M Houten; Tao Huang; Siwu Peng; Yong Zhao; Zhidong Tu; Jun Zhu
Journal:  Genome Med       Date:  2016-02-09       Impact factor: 11.117

Review 5.  Insights into the Neural and Genetic Basis of Vocal Communication.

Authors:  Genevieve Konopka; Todd F Roberts
Journal:  Cell       Date:  2016-03-10       Impact factor: 41.582

6.  Recent Advances in the Genetics of Vocal Learning.

Authors:  Michael C Condro; Stephanie A White
Journal:  Comp Cogn Behav Rev       Date:  2014

7.  Altered social behavior in mice carrying a cortical Foxp2 deletion.

Authors:  Vera P Medvedeva; Michael A Rieger; Beate Vieth; Cédric Mombereau; Christoph Ziegenhain; Tanay Ghosh; Arnaud Cressant; Wolfgang Enard; Sylvie Granon; Joseph D Dougherty; Matthias Groszer
Journal:  Hum Mol Genet       Date:  2019-03-01       Impact factor: 6.150

Review 8.  Nitric oxide signaling in the development and evolution of language and cognitive circuits.

Authors:  Owen H Funk; Kenneth Y Kwan
Journal:  Neurosci Res       Date:  2014-06-13       Impact factor: 3.304

9.  Sex hormone influence on human infants' sound characteristics: melody in spontaneous crying.

Authors:  Kathleen Wermke; Johannes Hain; Klaus Oehler; Peter Wermke; Volker Hesse
Journal:  Biol Lett       Date:  2014-05-07       Impact factor: 3.703

10.  An Etiological Foxp2 Mutation Impairs Neuronal Gain in Layer VI Cortico-Thalamic Cells through Increased GABAB/GIRK Signaling.

Authors:  Mélanie Druart; Matthias Groszer; Corentin Le Magueresse
Journal:  J Neurosci       Date:  2020-10-05       Impact factor: 6.167

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.