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Record W4410447561 · doi:10.1038/s41588-025-02184-4

Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption

2025· article· en· W4410447561 on OpenAlexafffund
Caroline Nava, Benjamin Cogné, Elsa Leitão, François Lecoquierre, Yuyang Chen, Sarah L. Stenton, Thomas Besnard, Solveig Heide, Sarah Baer, Abhilasha Jakhar, Sonja Neuser, Boris Keren, Anne Faudet, Sylvie Forlani, Marie Faoucher, Kévin Uguen, Konrad Platzer, Alexandra Afenjar, Jean‐Luc Alessandri, Stephanie Andres, Chloé Angelini, Bernard Aral, Benoı̂t Arveiler, Tania Attié‐Bitach, Marion Aubert‐Mucca, Guillaume Banneau, Tahsin Stefan Barakat, Giulia Barcia, Stéphanie Baulac, Claire Bénéteau, Fouzia Benkerdou, Virginie Bernard, Stéphane Bezieau, Dominique Bonneau, Marie-Noelle Bonnet-Dupeyron, Simon Boussion, Odile Boute, Elise Brischoux‐Boucher, Samantha J. Bryen, Julien Buratti, Tiffany Busa, Almuth Caliebe, Yline Capri, Kévin Cassinari, Roseline Caumes, Camille Cenni, Pascal Chambon, Perrine Charles, John Christodoulou, Cindy Colson, Solène Conrad, Auriane Cospain, Juliette Coursimault, Thomas Courtin, Madeline Couse, Charles Coutton, Isabelle Creveaux, Alissa M. D’Gama, Benjamin Dauriat, Jean‐Madeleine de Sainte Agathe, Giulia Gobbo, Andrée Delahaye‐Duriez, Julian Delanne, Anne‐Sophie Denommé‐Pichon, Anne Dieux‐Coëslier, Laura Do Souto Ferreira, Martine Doco‐Fenzy, Stephan Drukewitz, Véronique Duboc, Christèle Dubourg, Yannis Duffourd, David A. Dyment, Salima El Chehadeh, Monique Elmaleh, Laurence Faivre, Samuel Fennelly, Mélanie Fradin, Benjamin Ganne, Jamal Ghoumid, Himanshu Goel, Zeynep Gokce‐Samar, Alice Goldenberg, Svetlana Gorokhova, Louise Goujon, Victoria Granier, Mathilde Gras, John M. Greally, Bianca Greiten, Paul Gueguen, Anne‐Marie Guerrot, Saurav Guha, Anne Guimier, Tobias B. Haack, Hamza Hadj Abdallah, Yosra Halleb, Radu Harbuz, Madeleine Harris, Julia Hentschel, Bénédicte Héron, Marc‐Phillip Hitz, A. Micheil Innes, Vincent Jadas, Louis Januel, Nolwenn Jean‐Marçais, Vaidehi Jobanputra, Florence Jobic, Ludmila Jornéa, Sophie Julia, Frank J. Kaiser, Daniel Kaschta, Sabine Kaya, Petra Ketteler, Bochra Khadija, Fabian Kilpert, Cordula Knopp, Florian Kraft, Ilona Krey, Marilyn Lackmy, Fanny Laffargue, Laëtitia Lambert, Ryan E. Lamont, Vincent Laugel, Steven Laurie, Julie Lauzon, Louis Lebreton, Marine Lebrun, Marine Legendre, Éric Leguern, Daphné Lehalle, Élodie Lejeune, Gaëtan Lesca, Marion Lesieur‐Sebellin, Jonathan Lévy, Agnès Linglart, Stanislas Lyonnet, Kevin Lüthy, Alan Ma, Corinne Mach, Jean‐Louis Mandel, Lamisse Mansour‐Hendili, Julien Marcadier, V Terribile Wiel Marin, Henri Margot, Valentine Marquet, A. May, Johannes A. Mayr, Catherine Meridda, Vincent Michaud, Caroline Michot, Gwenaël Nadeau, Sophie Naudion, Mathilde Nizon, Frédérique Nowak, Sylvie Odent, Valérie Olin, Ikeoluwa Osei‐Owusu, Matthew Osmond, Katrin Õunap, Laurent Pasquier, Sandrine Passemard, M. Pauly, Olivier Patat, Marine Pensec, Laurence Perrin‐Sabourin, Florence Petit, Christophe Philippe, Marc Planes, Annapurna Poduri, Céline Poirsier, Antoine Pouzet, Bradley Prince, Clément Prouteau, Aurora Pujol, Caroline Racine, Mélanie Rama, Francis Ramond, Kara Ranguin, Margaux Raway, André Reis, Mathilde Renaud, Nicole Revençu, Anne‐Claire Richard, Lucile Riera-Navarro, Rocío Rius, Diana Rodriguez, Agustí Rodríguez‐Palmero, Sophie Rondeau, Annika Roser-Unruh, Hana Safraou, Véronique Satre, Pascale Saugier-Véber, Clément Sauvestre, Élise Schaefer, Wanqing Shao, Ina Schanze, Jan-Ulrich Schlump, Agatha Schlüter, Caroline Schluth‐Bolard, Sarah Schuhmann, Christopher Schröder, Monisha Sebastin, Sabine Sigaudy, Malte Spielmann, Marta Spodenkiewicz, Laura St Clair, Julie Steffann, Radka Stoeva, Harald Surowy, Mark A. Tarnopolsky, Calina Todosi, Annick Toutain, Frédéric Tran Mau‐Them, Astrid Unterlauft, Julien Van‐Gils, Clémence Vanlerberghe, Georgia Vasileiou, Gabriella Vera, André Verdel, Alain Verloès, Yoann Vial, Cédric Vignal, Marie Vincent, Catherine Vincent‐Delorme, Aline Vincent‐Devulder, Sacha Weber, Marjolaine Willems, Khaoula Zaafrane‐Khachnaoui, Pia Zacher, Lena Zeltner, Alban Ziegler, Wojciech P. Galej, Hélène Dollfus, Christel Thauvin‐Robinet, Kym M. Boycott, Pierre Marijon, Alban Lermine, Valérie Malan, Marlène Rio, Alma Kuechler, Bertrand Isidor, Séverine Drunat, Thomas Smol, Nicolas Chatron, Amélie Piton, Gaël Nicolas, Matias Wagner, Rami Abou Jamra, Delphine Héron, Cyril Mignot, Pierre Blanc, Anne O’Donnell‐Luria, Nicola Whiffin, Camille Charbonnier, Clément Charenton, Julien Thévenon, Christel Depienne

Bibliographic record

VenueNature Genetics · 2025
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicRNA Research and Splicing
Canadian institutionsMcMaster UniversityMcMaster Children's HospitalAlberta Children's HospitalUniversity of CalgaryChildren's Hospital of Eastern OntarioUniversity of OttawaHospital for Sick Children
FundersNational Human Genome Research InstituteCanadian Institutes of Health ResearchGenome AlbertaAlberta InnovatesAustrian Science FundZonMwInstitut National de la Santé et de la Recherche MédicaleEuropean CommissionMedical Research CouncilDepartment of Health and Social CareGeneralitat de CatalunyaNational Institute for Health and Care ResearchWellcome TrustCancer Research UKAlberta Children's Hospital FoundationGenome British ColumbiaCentres de Recerca de CatalunyaOntario Genomics InstituteAustralian GovernmentState Government of VictoriaCold Spring Harbor LaboratoryDeutsche ForschungsgemeinschaftChildren's Hospital FoundationRégion NormandieMurdoch Children's Research InstituteNew York Genome CenterGenome CanadaOntario GenomicsRoyal SocietyFundación HesperiaChildren’s Hospital of Wisconsin Research Institute
KeywordsBiologySpliceosomeRNA splicingGeneticsGeneSmall nuclear RNAIntronRNAComputational biologyNon-coding RNA

Abstract

fetched live from OpenAlex

The major spliceosome contains five small nuclear RNAs (snRNAs; U1, U2, U4, U5 and U6) essential for splicing. Variants in RNU4-2, encoding U4, cause a neurodevelopmental disorder called ReNU syndrome. We investigated de novo variants in 50 snRNA-encoding genes in a French cohort of 23,649 individuals with rare disorders and gathered additional cases through international collaborations. Altogether, we identified 145 previously unreported probands with (likely) pathogenic variants in RNU4-2 and 21 individuals with de novo and/or recurrent variants in RNU5B-1 and RNU5A-1, encoding U5. Pathogenic variants typically arose de novo on the maternal allele and cluster in regions critical for splicing. RNU4-2 variants mainly localize to two structures, the stem III and T-loop/quasi-pseudoknot, which position the U6 ACAGAGA box for 5' splice site recognition and associate with different phenotypic severity. RNU4-2 variants result in specific defects in alternative 5' splice site usage and methylation patterns (episignatures) that correlate with variant location and clinical severity. This study establishes RNU5B-1 as a neurodevelopmental disorder gene, suggests RNU5A-1 as a strong candidate and highlights the role of de novo variants in snRNAs.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.732
Threshold uncertainty score0.818

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.008
GPT teacher head0.271
Teacher spread0.263 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations42
Published2025
Admission routes2
Has abstractyes

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