Literature DB >> 35358416

De novo variants in ATP2B1 lead to neurodevelopmental delay.

Meer Jacob Rahimi1, Nicole Urban2, Meret Wegler1, Heinrich Sticht3, Michael Schaefer2, Bernt Popp1, Frank Gaunitz4, Manuela Morleo5, Vincenzo Nigro5, Silvia Maitz6, Grazia M S Mancini7, Claudia Ruivenkamp8, Eun-Kyung Suk9, Tobias Bartolomaeus10, Andreas Merkenschlager11, Daniel Koboldt12, Dennis Bartholomew13, Alexander P A Stegmann14, Margje Sinnema14, Irma Duynisveld15, Ramona Salvarinova16, Simone Race16, Bert B A de Vries17, Aurélien Trimouille18, Sophie Naudion19, Daphna Marom20, Uri Hamiel20, Noa Henig20, Florence Demurger21, Nils Rahner22, Enrika Bartels22, J Austin Hamm23, Abbey M Putnam23, Richard Person24, Rami Abou Jamra1, Henry Oppermann25.   

Abstract

Calcium (Ca2+) is a universal second messenger involved in synaptogenesis and cell survival; consequently, its regulation is important for neurons. ATPase plasma membrane Ca2+ transporting 1 (ATP2B1) belongs to the family of ATP-driven calmodulin-dependent Ca2+ pumps that participate in the regulation of intracellular free Ca2+. Here, we clinically describe a cohort of 12 unrelated individuals with variants in ATP2B1 and an overlapping phenotype of mild to moderate global development delay. Additional common symptoms include autism, seizures, and distal limb abnormalities. Nine probands harbor missense variants, seven of which were in specific functional domains, and three individuals have nonsense variants. 3D structural protein modeling suggested that the variants have a destabilizing effect on the protein. We performed Ca2+ imaging after introducing all nine missense variants in transfected HEK293 cells and showed that all variants lead to a significant decrease in Ca2+ export capacity compared with the wild-type construct, thus proving their pathogenicity. Furthermore, we observed for the same variant set an incorrect intracellular localization of ATP2B1. The genetic findings and the overlapping phenotype of the probands as well as the functional analyses imply that de novo variants in ATP2B1 lead to a monogenic form of neurodevelopmental disorder.
Copyright © 2022 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ATP2B1; abnormal behavior; calcium homeostasis; de novo; development delay; intellectual disability; neurodevelopmental disorder; seizure

Mesh:

Substances:

Year:  2022        PMID: 35358416      PMCID: PMC9118097          DOI: 10.1016/j.ajhg.2022.03.009

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.043


  31 in total

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Authors:  Sertac N Kip; Noah W Gray; Alain Burette; Ali Canbay; Richard J Weinberg; Emanuel E Strehler
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Journal:  Am J Med Genet A       Date:  2005-11-01       Impact factor: 2.802

3.  Genome sequencing identifies major causes of severe intellectual disability.

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Journal:  Nature       Date:  2014-06-04       Impact factor: 49.962

4.  Cellular and subcellular localization of the neuron-specific plasma membrane calcium ATPase PMCA1a in the rat brain.

Authors:  Katharine A Kenyon; Eric A Bushong; Amy S Mauer; Emanuel E Strehler; Richard J Weinberg; Alain C Burette
Journal:  J Comp Neurol       Date:  2010-08-15       Impact factor: 3.215

5.  Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.

Authors:  Kathleen M Gorman; Esther Meyer; Detelina Grozeva; Egidio Spinelli; Amy McTague; Alba Sanchis-Juan; Keren J Carss; Emily Bryant; Adi Reich; Amy L Schneider; Ronit M Pressler; Michael A Simpson; Geoff D Debelle; Evangeline Wassmer; Jenny Morton; Diana Sieciechowicz; Eric Jan-Kamsteeg; Alex R Paciorkowski; Mary D King; J Helen Cross; Annapurna Poduri; Heather C Mefford; Ingrid E Scheffer; Tobias B Haack; Gary McCullagh; John J Millichap; Gemma L Carvill; Jill Clayton-Smith; Eamonn R Maher; F Lucy Raymond; Manju A Kurian
Journal:  Am J Hum Genet       Date:  2019-04-11       Impact factor: 11.025

6.  Prevalence and architecture of de novo mutations in developmental disorders.

Authors: 
Journal:  Nature       Date:  2017-01-25       Impact factor: 49.962

7.  MetaDome: Pathogenicity analysis of genetic variants through aggregation of homologous human protein domains.

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8.  Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.

Authors:  Korinna Kochinke; Christiane Zweier; Bonnie Nijhof; Michaela Fenckova; Pavel Cizek; Frank Honti; Shivakumar Keerthikumar; Merel A W Oortveld; Tjitske Kleefstra; Jamie M Kramer; Caleb Webber; Martijn A Huynen; Annette Schenck
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Review 9.  Neuronal calcium signaling: function and dysfunction.

Authors:  Marisa Brini; Tito Calì; Denis Ottolini; Ernesto Carafoli
Journal:  Cell Mol Life Sci       Date:  2014-01-19       Impact factor: 9.261

10.  The mutational constraint spectrum quantified from variation in 141,456 humans.

Authors:  Konrad J Karczewski; Laurent C Francioli; Grace Tiao; Beryl B Cummings; Jessica Alföldi; Qingbo Wang; Ryan L Collins; Kristen M Laricchia; Andrea Ganna; Daniel P Birnbaum; Laura D Gauthier; Harrison Brand; Matthew Solomonson; Nicholas A Watts; Daniel Rhodes; Moriel Singer-Berk; Eleina M England; Eleanor G Seaby; Jack A Kosmicki; Raymond K Walters; Katherine Tashman; Yossi Farjoun; Eric Banks; Timothy Poterba; Arcturus Wang; Cotton Seed; Nicola Whiffin; Jessica X Chong; Kaitlin E Samocha; Emma Pierce-Hoffman; Zachary Zappala; Anne H O'Donnell-Luria; Eric Vallabh Minikel; Ben Weisburd; Monkol Lek; James S Ware; Christopher Vittal; Irina M Armean; Louis Bergelson; Kristian Cibulskis; Kristen M Connolly; Miguel Covarrubias; Stacey Donnelly; Steven Ferriera; Stacey Gabriel; Jeff Gentry; Namrata Gupta; Thibault Jeandet; Diane Kaplan; Christopher Llanwarne; Ruchi Munshi; Sam Novod; Nikelle Petrillo; David Roazen; Valentin Ruano-Rubio; Andrea Saltzman; Molly Schleicher; Jose Soto; Kathleen Tibbetts; Charlotte Tolonen; Gordon Wade; Michael E Talkowski; Benjamin M Neale; Mark J Daly; Daniel G MacArthur
Journal:  Nature       Date:  2020-05-27       Impact factor: 69.504

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1.  The ataxia-linked E1081Q mutation affects the sub-plasma membrane Ca2+-microdomains by tuning PMCA3 activity.

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  1 in total

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