Literature DB >> 28053010

Mutations in GABRB3: From febrile seizures to epileptic encephalopathies.

Rikke S Møller1, Thomas V Wuttke2, Ingo Helbig2, Carla Marini2, Katrine M Johannesen2, Eva H Brilstra2, Ulvi Vaher2, Ingo Borggraefe2, Inga Talvik2, Tiina Talvik2, Gerhard Kluger2, Laurence L Francois2, Gaetan Lesca2, Julitta de Bellescize2, Susanne Blichfeldt2, Nicolas Chatron2, Nils Holert2, Julia Jacobs2, Marielle Swinkels2, Cornelia Betzler2, Steffen Syrbe2, Marina Nikanorova2, Candace T Myers2, Line H G Larsen2, Sabina Vejzovic2, Manuela Pendziwiat2, Sarah von Spiczak2, Sarah Hopkins2, Holly Dubbs2, Yuan Mang2, Konstantin Mukhin2, Hans Holthausen2, Koen L van Gassen2, Hans A Dahl2, Niels Tommerup2, Heather C Mefford2, Guido Rubboli2, Renzo Guerrini2, Johannes R Lemke2, Holger Lerche2, Hiltrud Muhle2, Snezana Maljevic2.   

Abstract

OBJECTIVE: To examine the role of mutations in GABRB3 encoding the β3 subunit of the GABAA receptor in individual patients with epilepsy with regard to causality, the spectrum of genetic variants, their pathophysiology, and associated phenotypes.
METHODS: We performed massive parallel sequencing of GABRB3 in 416 patients with a range of epileptic encephalopathies and childhood-onset epilepsies and recruited additional patients with epilepsy with GABRB3 mutations from other research and diagnostic programs.
RESULTS: We identified 22 patients with heterozygous mutations in GABRB3, including 3 probands from multiplex families. The phenotypic spectrum of the mutation carriers ranged from simple febrile seizures, genetic epilepsies with febrile seizures plus, and epilepsy with myoclonic-atonic seizures to West syndrome and other types of severe, early-onset epileptic encephalopathies. Electrophysiologic analysis of 7 mutations in Xenopus laevis oocytes, using coexpression of wild-type or mutant β3, together with α5 and γ2s subunits and an automated 2-microelectrode voltage-clamp system, revealed reduced GABA-induced current amplitudes or GABA sensitivity for 5 of 7 mutations.
CONCLUSIONS: Our results indicate that GABRB3 mutations are associated with a broad phenotypic spectrum of epilepsies and that reduced receptor function causing GABAergic disinhibition represents the relevant disease mechanism.
© 2017 American Academy of Neurology.

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Year:  2017        PMID: 28053010      PMCID: PMC5278942          DOI: 10.1212/WNL.0000000000003565

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  39 in total

1.  GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.

Authors:  Gemma L Carvill; Sarah Weckhuysen; Jacinta M McMahon; Corinna Hartmann; Rikke S Møller; Helle Hjalgrim; Joseph Cook; Eileen Geraghty; Brian J O'Roak; Steve Petrou; Alison Clarke; Deepak Gill; Lynette G Sadleir; Hiltrud Muhle; Sarah von Spiczak; Marina Nikanorova; Bree L Hodgson; Elena V Gazina; Arvid Suls; Jay Shendure; Leanne M Dibbens; Peter De Jonghe; Ingo Helbig; Samuel F Berkovic; Ingrid E Scheffer; Heather C Mefford
Journal:  Neurology       Date:  2014-03-12       Impact factor: 9.910

2.  Centrencephalic myoclonic-astatic petit mal. Clinical and genetic investigation.

Authors:  H Doose; H Gerken; R Leonhardt; E Völzke; C Völz
Journal:  Neuropadiatrie       Date:  1970-08

3.  A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.

Authors:  A Escayg; A Heils; B T MacDonald; K Haug; T Sander; M H Meisler
Journal:  Am J Hum Genet       Date:  2001-03-14       Impact factor: 11.025

4.  Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsy.

Authors:  Saul A Mullen; Carla Marini; Arvid Suls; Davide Mei; Elvio Della Giustina; Daniela Buti; Todor Arsov; John Damiano; Kate Lawrence; Peter De Jonghe; Samuel F Berkovic; Ingrid E Scheffer; Renzo Guerrini
Journal:  Arch Neurol       Date:  2011-05-09

5.  Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies.

Authors:  Rikke S Møller; Line H G Larsen; Katrine M Johannesen; Inga Talvik; Tiina Talvik; Ulvi Vaher; Maria J Miranda; Muhammad Farooq; Jens E K Nielsen; Lene Lavard Svendsen; Ditte B Kjelgaard; Karen M Linnet; Qin Hao; Peter Uldall; Mimoza Frangu; Niels Tommerup; Shahid M Baig; Uzma Abdullah; Alfred P Born; Pia Gellert; Marina Nikanorova; Kern Olofsson; Birgit Jepsen; Dragan Marjanovic; Lana I K Al-Zehhawi; Sofia J Peñalva; Bente Krag-Olsen; Klaus Brusgaard; Helle Hjalgrim; Guido Rubboli; Deb K Pal; Hans A Dahl
Journal:  Mol Syndromol       Date:  2016-08-20

6.  Differential molecular and behavioural alterations in mouse models of GABRG2 haploinsufficiency versus dominant negative mutations associated with human epilepsy.

Authors:  Timothy A Warner; Wangzhen Shen; Xuan Huang; Zhong Liu; Robert L Macdonald; Jing-Qiong Kang
Journal:  Hum Mol Genet       Date:  2016-06-23       Impact factor: 6.150

7.  Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

Authors:  R H Wallace; D W Wang; R Singh; I E Scheffer; A L George; H A Phillips; K Saar; A Reis; E W Johnson; G R Sutherland; S F Berkovic; J C Mulley
Journal:  Nat Genet       Date:  1998-08       Impact factor: 38.330

8.  A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions.

Authors:  Colette Kananura; Karsten Haug; Thomas Sander; Uwe Runge; Wenli Gu; Kerstin Hallmann; Johannes Rebstock; Armin Heils; Ortrud K Steinlein
Journal:  Arch Neurol       Date:  2002-07

9.  Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome.

Authors:  Moran Rubinstein; Ruth E Westenbroek; Frank H Yu; Christina J Jones; Todd Scheuer; William A Catterall
Journal:  Neurobiol Dis       Date:  2014-10-02       Impact factor: 5.996

10.  De novo mutations in epileptic encephalopathies.

Authors:  Andrew S Allen; Samuel F Berkovic; Patrick Cossette; Norman Delanty; Dennis Dlugos; Evan E Eichler; Michael P Epstein; Tracy Glauser; David B Goldstein; Yujun Han; Erin L Heinzen; Yuki Hitomi; Katherine B Howell; Michael R Johnson; Ruben Kuzniecky; Daniel H Lowenstein; Yi-Fan Lu; Maura R Z Madou; Anthony G Marson; Heather C Mefford; Sahar Esmaeeli Nieh; Terence J O'Brien; Ruth Ottman; Slavé Petrovski; Annapurna Poduri; Elizabeth K Ruzzo; Ingrid E Scheffer; Elliott H Sherr; Christopher J Yuskaitis; Bassel Abou-Khalil; Brian K Alldredge; Jocelyn F Bautista; Samuel F Berkovic; Alex Boro; Gregory D Cascino; Damian Consalvo; Patricia Crumrine; Orrin Devinsky; Dennis Dlugos; Michael P Epstein; Miguel Fiol; Nathan B Fountain; Jacqueline French; Daniel Friedman; Eric B Geller; Tracy Glauser; Simon Glynn; Sheryl R Haut; Jean Hayward; Sandra L Helmers; Sucheta Joshi; Andres Kanner; Heidi E Kirsch; Robert C Knowlton; Eric H Kossoff; Rachel Kuperman; Ruben Kuzniecky; Daniel H Lowenstein; Shannon M McGuire; Paul V Motika; Edward J Novotny; Ruth Ottman; Juliann M Paolicchi; Jack M Parent; Kristen Park; Annapurna Poduri; Ingrid E Scheffer; Renée A Shellhaas; Elliott H Sherr; Jerry J Shih; Rani Singh; Joseph Sirven; Michael C Smith; Joseph Sullivan; Liu Lin Thio; Anu Venkat; Eileen P G Vining; Gretchen K Von Allmen; Judith L Weisenberg; Peter Widdess-Walsh; Melodie R Winawer
Journal:  Nature       Date:  2013-08-11       Impact factor: 49.962

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  29 in total

1.  The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures.

Authors:  Rosemary Burgess; Shuyu Wang; Amy McTague; Katja E Boysen; Xiaoling Yang; Qi Zeng; Kenneth A Myers; Anne Rochtus; Marina Trivisano; Deepak Gill; Lynette G Sadleir; Nicola Specchio; Renzo Guerrini; Carla Marini; Yue-Hua Zhang; Heather C Mefford; Manju A Kurian; Annapurna H Poduri; Ingrid E Scheffer
Journal:  Ann Neurol       Date:  2019-12       Impact factor: 10.422

2.  NBEA: Developmental disease gene with early generalized epilepsy phenotypes.

Authors:  Maureen S Mulhern; Constance Stumpel; Nicholas Stong; Han G Brunner; Louise Bier; Natalie Lippa; James Riviello; Rob P W Rouhl; Marlies Kempers; Rolph Pfundt; Alexander P A Stegmann; Mary K Kukolich; Aida Telegrafi; Anna Lehman; Elena Lopez-Rangel; Nada Houcinat; Magalie Barth; Nicolette den Hollander; Mariette J V Hoffer; Sarah Weckhuysen; Jolien Roovers; Tania Djemie; Diana Barca; Berten Ceulemans; Dana Craiu; Johannes R Lemke; Christian Korff; Heather C Mefford; Candace T Meyers; Zsuzsanna Siegler; Susan M Hiatt; Gregory M Cooper; E Martina Bebin; Lot Snijders Blok; Hermine E Veenstra-Knol; Evan H Baugh; Eva H Brilstra; Catharina M L Volker-Touw; Ellen van Binsbergen; Anya Revah-Politi; Elaine Pereira; Danielle McBrian; Mathilde Pacault; Bertrand Isidor; Cedric Le Caignec; Brigitte Gilbert-Dussardier; Frederic Bilan; Erin L Heinzen; David B Goldstein; Servi J C Stevens; Tristan T Sands
Journal:  Ann Neurol       Date:  2018-10-25       Impact factor: 10.422

Review 3.  Ion Channels in Genetic Epilepsy: From Genes and Mechanisms to Disease-Targeted Therapies.

Authors:  Julia Oyrer; Snezana Maljevic; Ingrid E Scheffer; Samuel F Berkovic; Steven Petrou; Christopher A Reid
Journal:  Pharmacol Rev       Date:  2018-01       Impact factor: 25.468

Review 4.  Rett Syndrome Spectrum in Monogenic Developmental-Epileptic Encephalopathies and Epilepsies: A Review.

Authors:  Carlotta Spagnoli; Carlo Fusco; Francesco Pisani
Journal:  Genes (Basel)       Date:  2021-07-28       Impact factor: 4.096

Review 5.  Defects at the crossroads of GABAergic signaling in generalized genetic epilepsies.

Authors:  Jing-Qiong Kang
Journal:  Epilepsy Res       Date:  2017-08-26       Impact factor: 3.045

6.  Spatial Clustering of de Novo Missense Mutations Identifies Candidate Neurodevelopmental Disorder-Associated Genes.

Authors:  Stefan H Lelieveld; Laurens Wiel; Hanka Venselaar; Rolph Pfundt; Gerrit Vriend; Joris A Veltman; Han G Brunner; Lisenka E L M Vissers; Christian Gilissen
Journal:  Am J Hum Genet       Date:  2017-08-31       Impact factor: 11.025

7.  Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies.

Authors:  Ciria C Hernandez; Wenshu XiangWei; Ningning Hu; Dingding Shen; Wangzhen Shen; Andre H Lagrange; Yujia Zhang; Lifang Dai; Changhong Ding; Zhaohui Sun; Jiasheng Hu; Hongmin Zhu; Yuwu Jiang; Robert L Macdonald
Journal:  Brain       Date:  2019-07-01       Impact factor: 13.501

8.  De novo variants in GABRA2 and GABRA5 alter receptor function and contribute to early-onset epilepsy.

Authors:  Kameryn M Butler; Olivia A Moody; Elisabeth Schuler; Jason Coryell; John J Alexander; Andrew Jenkins; Andrew Escayg
Journal:  Brain       Date:  2018-08-01       Impact factor: 13.501

9.  Biallelic inherited SCN8A variants, a rare cause of SCN8A-related developmental and epileptic encephalopathy.

Authors:  Eric R Wengert; Cathrine E Tronhjem; Jacy L Wagnon; Katrine M Johannesen; Hayley Petit; Ilona Krey; Anusha U Saga; Payal S Panchal; Samantha M Strohm; Jörn Lange; Susanne B Kamphausen; Guido Rubboli; Johannes R Lemke; Elena Gardella; Manoj K Patel; Miriam H Meisler; Rikke S Møller
Journal:  Epilepsia       Date:  2019-10-17       Impact factor: 5.864

10.  Dravet syndrome-associated mutations in GABRA1, GABRB2 and GABRG2 define the genetic landscape of defects of GABAA receptors.

Authors:  Ciria C Hernandez; XiaoJuan Tian; Ningning Hu; Wangzhen Shen; Mackenzie A Catron; Ying Yang; Jiaoyang Chen; Yuwu Jiang; Yuehua Zhang; Robert L Macdonald
Journal:  Brain Commun       Date:  2021-03-11
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