Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndrome.

TitleHaploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndrome.
Publication TypeJournal Article
Year of Publication2012
AuthorsBernier, FP, Caluseriu, O, Ng, S, Schwartzentruber, J, Buckingham, KJ, A Innes, M, Jabs, EWang, Innis, JW, Schuette, JL, Gorski, JL, Byers, PH, Andelfinger, G, Siu, V, Lauzon, J, Fernandez, BA, McMillin, M, Scott, RH, Racher, H, Majewski, J, Nickerson, DA, Shendure, J, Bamshad, MJ, Parboosingh, JS
Corporate AuthorsFORGE Canada Consortium
JournalAm J Hum Genet
Volume90
Issue5
Pagination925-33
Date Published2012 May 04
ISSN1537-6605
KeywordsAdult, Child, Child, Preschool, Cohort Studies, Exome, Female, Haploinsufficiency, Humans, Limb Deformities, Congenital, Male, Mandibulofacial Dysostosis, Mutation, Reproducibility of Results, RNA Precursors, RNA Splicing Factors, RNA-Binding Proteins, Spliceosomes, Young Adult
Abstract

Nager syndrome, first described more than 60 years ago, is the archetype of a class of disorders called the acrofacial dysostoses, which are characterized by craniofacial and limb malformations. Despite intensive efforts, no gene for Nager syndrome has yet been identified. In an international collaboration, FORGE Canada and the National Institutes of Health Centers for Mendelian Genomics used exome sequencing as a discovery tool and found that mutations in SF3B4, a component of the U2 pre-mRNA spliceosomal complex, cause Nager syndrome. After Sanger sequencing of SF3B4 in a validation cohort, 20 of 35 (57%) families affected by Nager syndrome had 1 of 18 different mutations, nearly all of which were frameshifts. These results suggest that most cases of Nager syndrome are caused by haploinsufficiency of SF3B4. Our findings add Nager syndrome to a growing list of disorders caused by mutations in genes that encode major components of the spliceosome and also highlight the synergistic potential of international collaboration when exome sequencing is applied in the search for genes responsible for rare Mendelian phenotypes.

DOI10.1016/j.ajhg.2012.04.004
Alternate JournalAm. J. Hum. Genet.
PubMed ID22541558
PubMed Central IDPMC3376638
Grant ListK99 HG004316 / HG / NHGRI NIH HHS / United States
U54 HG006493 / HG / NHGRI NIH HHS / United States
RC2 HG005608 / HG / NHGRI NIH HHS / United States
1R01HD048895 / HD / NICHD NIH HHS / United States
1RC2HG005608 / HG / NHGRI NIH HHS / United States
R00 HG004316 / HG / NHGRI NIH HHS / United States
/ / Canadian Institutes of Health Research / Canada
R01 HD048895 / HD / NICHD NIH HHS / United States
UM1 HG006493 / HG / NHGRI NIH HHS / United States
1U54HG006493 / HG / NHGRI NIH HHS / United States
5R01HG004316 / HG / NHGRI NIH HHS / United States