A relatively common homozygous TRAPPC4 splicing variant is associated with an early-infantile neurodegenerative syndrome.

TitleA relatively common homozygous TRAPPC4 splicing variant is associated with an early-infantile neurodegenerative syndrome.
Publication TypeJournal Article
Year of Publication2021
AuthorsGhosh, SG, Scala, M, Beetz, C, Helman, G, Stanley, V, Yang, X, Breuss, MW, Mazaheri, N, Selim, L, Hadipour, F, Pais, L, Stutterd, CA, Karageorgou, V, Begtrup, A, Crunk, A, Juusola, J, Willaert, R, Flore, LA, Kennelly, K, Spencer, C, Brown, M, Trapane, P, Hurst, ACE, S Rutledge, L, Goodloe, DH, McDonald, MT, Shashi, V, Schoch, K, Tomoum, H, Zaitoun, R, Hadipour, Z, Galehdari, H, Pagnamenta, AT, Mojarrad, M, Sedaghat, A, Dias, P, Quintas, S, Eslahi, A, Shariati, G, Bauer, P, Simons, C, Houlden, H, Issa, MY, Zaki, MAHS, Maroofian, R, Gleeson, JG
Corporate AuthorsUndiagnosed Diseases Network
JournalEur J Hum Genet
Volume29
Issue2
Pagination271-279
Date Published2021 Feb
ISSN1476-5438
Abstract

Trafficking protein particle (TRAPP) complexes, which include the TRAPPC4 protein, regulate membrane trafficking between lipid organelles in a process termed vesicular tethering. TRAPPC4 was recently implicated in a recessive neurodevelopmental condition in four unrelated families due to a shared c.454+3A>G splice variant. Here, we report 23 patients from 17 independent families with an early-infantile-onset neurodegenerative presentation, where we also identified the homozygous variant hg38:11:119020256 A>G (NM_016146.5:c.454+3A>G) in TRAPPC4 through exome or genome sequencing. No other clinically relevant TRAPPC4 variants were identified among any of over 10,000 patients with neurodevelopmental conditions. We found the carrier frequency of TRAPPC4 c.454+3A>G was 2.4-5.4 per 10,000 healthy individuals. Affected individuals with the homozygous TRAPPC4 c.454+3A>G variant showed profound psychomotor delay, developmental regression, early-onset epilepsy, microcephaly and progressive spastic tetraplegia. Based upon RNA sequencing, the variant resulted in partial exon 3 skipping and generation of an aberrant transcript owing to use of a downstream cryptic splice donor site, predicting a premature stop codon and nonsense mediated decay. These data confirm the pathogenicity of the TRAPPC4 c.454+3A>G variant, and refine the clinical presentation of TRAPPC4-related encephalopathy.

DOI10.1038/s41431-020-00717-5
Alternate JournalEur J Hum Genet
PubMed ID32901138
PubMed Central IDPMC7868361
Grant ListMR/S01165X/1 / / RCUK | Medical Research Council (MRC) /
UM1 HG008900 / HG / NHGRI NIH HHS / United States
R01NS106387 / / U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) /
R01 NS098004 / NS / NINDS NIH HHS / United States
F31HD095602 / / U.S. Department of Health & Human Services | NIH | National Institute on Deafness and Other Communication Disorders (NIDCD) /
U01 HG007672 / HG / NHGRI NIH HHS / United States
MR/S005021/1 / / RCUK | Medical Research Council (MRC) /
G0601943 / / RCUK | Medical Research Council (MRC) /
R01 NS048453 / NS / NINDS NIH HHS / United States