De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

• Published in: medRxiv : the preprint server for health sciences
• Main Authors: Chen, Yuyang, Dawes, Ruebena, Kim, Hyung Chul, Stenton, Sarah L, Walker, Susan, Ljungdahl, Alicia, Lord, Jenny, Ganesh, Vijay S, Ma, Jialan, Martin-Geary, Alexandra C, Lemire, Gabrielle, D'Souza, Elston N, Dong, Shan, Ellingford, Jamie M, Adams, David R, Allan, Kirsten, Bakshi, Madhura, Baldwin, Erin E, Berger, Seth I, Bernstein, Jonathan A, Brown, Natasha J, Burrage, Lindsay C, Chapman, Kimberly, Compton, Alison G, Cunningham, Chloe A, D'Souza, Precilla, Délot, Emmanuèle C, Dias, Kerith-Rae, Elias, Ellen R, Evans, Carey-Anne, Ewans, Lisa, Ezell, Kimberly, Fraser, Jamie L, Gallacher, Lyndon, Genetti, Casie A, Grant, Christina L, Haack, Tobias, Kuechler, Alma, Lalani, Seema R, Leitão, Elsa, Fevre, Anna Le, Leventer, Richard J, Liebelt, Jan E, Lockhart, Paul J, Ma, Alan S, Macnamara, Ellen F, Maurer, Taylor M, Mendez, Hector R, Montgomery, Stephen B, Nassogne, Marie-Cécile, Neumann, Serena, O'Leary, Melanie, Palmer, Elizabeth E, Phillips, John, Pitsava, Georgia, Pysar, Ryan, Rehm, Heidi L, Reuter, Chloe M, Revencu, Nicole, Riess, Angelika, Rius, Rocio, Rodan, Lance, Roscioli, Tony, Rosenfeld, Jill A, Sachdev, Rani, Simons, Cas, Sisodiya, Sanjay M, Snell, Penny, Clair, Laura, Stark, Zornitza, Tan, Tiong Yang, Tan, Natalie B, Temple, Suzanna El, Thorburn, David R, Tifft, Cynthia J, Uebergang, Eloise, VanNoy, Grace E, Vilain, Eric, Viskochil, David H, Wedd, Laura, Wheeler, Matthew T, White, Susan M, Wojcik, Monica, Wolfe, Lynne A, Wolfenson, Zoe, Xiao, Changrui, Zocche, David, Rubenstein, John L, Markenscoff-Papadimitriou, Eirene, Fica, Sebastian M, Baralle, Diana, Depienne, Christel, MacArthur, Daniel G, Howson, Joanna Mm, Sanders, Stephan J, O'Donnell-Luria, Anne, Whiffin, Nicola
• Format: Journal Article
• Language: English
• Published: United States 09.04.2024

Around 60% of individuals with neurodevelopmental disorders (NDD) remain undiagnosed after comprehensive genetic testing, primarily of protein-coding genes . Increasingly, large genome-sequenced cohorts are improving our ability to discover new diagnoses in the non-coding genome. Here, we identify the non-coding RNA as a novel syndromic NDD gene. encodes the U4 small nuclear RNA (snRNA), which is a critical component of the U4/U6.U5 tri-snRNP complex of the major spliceosome . We identify an 18 bp region of mapping to two structural elements in the U4/U6 snRNA duplex (the T-loop and Stem III) that is severely depleted of variation in the general population, but in which we identify heterozygous variants in 119 individuals with NDD. The vast majority of individuals (77.3%) have the same highly recurrent single base-pair insertion (n.64_65insT). We estimate that variants in this region explain 0.41% of individuals with NDD. We demonstrate that is highly expressed in the developing human brain, in contrast to its contiguous counterpart and other U4 homologs, supporting 's role as the primary U4 transcript in the brain. Overall, this work underscores the importance of non-coding genes in rare disorders. It will provide a diagnosis to thousands of individuals with NDD worldwide and pave the way for the development of effective treatments for these individuals.