Title | Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndrome. |
Publication Type | Journal Article |
Year of Publication | 2012 |
Authors | Bernier, 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 Authors | FORGE Canada Consortium |
Journal | Am J Hum Genet |
Volume | 90 |
Issue | 5 |
Pagination | 925-33 |
Date Published | 2012 May 04 |
ISSN | 1537-6605 |
Keywords | Adult, 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. |
DOI | 10.1016/j.ajhg.2012.04.004 |
Alternate Journal | Am. J. Hum. Genet. |
PubMed ID | 22541558 |
PubMed Central ID | PMC3376638 |
Grant List | K99 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 |