TY - JOUR
T1 - Mutations in the U2 snRNA gene
RNU2-2P cause a severe neurodevelopmental disorder with prominent epilepsy.
AU - Greene, Daniel
AU - De Wispelaere, Koenraad
AU - Lees, Jon
AU - Katrinecz, Andrea
AU - Pascoal, Sonia
AU - Hales, Emma
AU - Codina-Solà, Marta
AU - Valenzuela, Irene
AU - Tizzano, Eduardo F
AU - Atton, Giles
AU - Donnelly, Deirdre
AU - Foulds, Nicola
AU - Jarvis, Joanna
AU - McKee, Shane
AU - O'Donoghue, Michael
AU - Suri, Mohnish
AU - Vasudevan, Pradeep
AU - Stirrups, Kathy
AU - Morgan, Natasha P
AU - Freson, Kathleen
AU - Mumford, Andrew D
AU - Turro, Ernest
PY - 2024/9/4
Y1 - 2024/9/4
N2 - The major spliceosome comprises the five snRNAs U1, U2, U4, U5 and U6. We recently showed that mutations in
RNU4- 2, which encodes U4 snRNA, cause one of the most prevalent monogenic neurodevelopmental disorders. Here, we report that recurrent germline mutations in
RNU2-2P , a 191bp gene encoding U2 snRNA, are responsible for a related disorder. By genetic association, we implicated recurrent
de novo single nucleotide mutations at nucleotide positions 4 and 35 of
RNU2-2P among nine cases. We replicated this finding in six additional cases, bringing the total to 15. The disorder is characterized by intellectual disability, neurodevelopmental delay, autistic behavior, microcephaly, hypotonia, epilepsy and hyperventilation. All cases display a severe and complex seizure phenotype. Our findings cement the role of major spliceosomal snRNAs in the etiologies of neurodevelopmental disorders.
AB - The major spliceosome comprises the five snRNAs U1, U2, U4, U5 and U6. We recently showed that mutations in
RNU4- 2, which encodes U4 snRNA, cause one of the most prevalent monogenic neurodevelopmental disorders. Here, we report that recurrent germline mutations in
RNU2-2P , a 191bp gene encoding U2 snRNA, are responsible for a related disorder. By genetic association, we implicated recurrent
de novo single nucleotide mutations at nucleotide positions 4 and 35 of
RNU2-2P among nine cases. We replicated this finding in six additional cases, bringing the total to 15. The disorder is characterized by intellectual disability, neurodevelopmental delay, autistic behavior, microcephaly, hypotonia, epilepsy and hyperventilation. All cases display a severe and complex seizure phenotype. Our findings cement the role of major spliceosomal snRNAs in the etiologies of neurodevelopmental disorders.
U2 - 10.1101/2024.09.03.24312863
DO - 10.1101/2024.09.03.24312863
M3 - Article (Academic Journal)
C2 - 39281759
JO - medRxiv
JF - medRxiv
ER -