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European journal of human genetics : EJHG · 2025

Heterozygous CELF4 variants in the N-term region crucial for the RNA-binding activity lead to neurodevelopmental disorder and obesity.

СтатьяНазвание и аннотация: Перевод в очереди
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Bruel Ange-Line, Vulto-vanSilfhout Anneke T, Bilan Frédéric, Le Guyader Gwenaël, Gilbert-Dussardier Brigitte, Le Guillou Xavier, Rondeau Sophie, Rio Marlène, Lee Kristen N, Beil Adelyn, Suri Mohnish, Guerin François, Ruault Valentin, Goldenberg Alice, Lecoquierre François, Bertsch Nicole, Anderson Rhonda, Yang Xiao-Ru, Inness Micheil, Rikeros-Orozco Emi, Palomares-Bralo Maria, Hayek Jennifer Cassady, Cech Jennifer, Jhuraney Ankita, Kumar Runjun D, Mercimek-Andrews Saadet, Ambrose Anastasia, Wakeling Erin N, Wentzensen Ingrid M, Torti Erin, Gooch Catherine, Faivre Laurence, Philippe Christophe, Duffourd Yannis, Vitobello Antonio, Thauvin-Robinet Christel

Аннотация

RNA-binding proteins play a key role in post-transcriptional events, such as mRNA splicing, transport, stability, translation and decay. Dysregulation of RNA life can have dramatic consequences. CELF RNA-binding proteins appear to be essential during embryo development. In this study, we identified 15 patients with heterozygous missense or loss-of-function variants in the CELF4 gene by exome or genome sequencing. All variants affecting the N-terminus of the protein are essential and sufficient for the RNA-binding and splicing activity or RRM domains. Most patients presented with neurodevelopmental disorders including global developmental delay/intellectual disability (11/14), seizures (9/15) and overweight/obesity (10/14) that began in childhood. Clinical features are similar to the reported celf4-mouse mutant phenotype. This study highlights the essential role of CELF4 in development and its involvement as a novel etiology of neurodevelopmental disorders with obesity.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты