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XB-ART-58326
Nat Commun 2021 Aug 03;121:4680. doi: 10.1038/s41467-021-24852-9.
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Haploinsufficiency of SF3B2 causes craniofacial microsomia.

Timberlake AT , Griffin C , Heike CL , Hing AV , Cunningham ML , Chitayat D , Davis MR , Doust SJ , Drake AF , Duenas-Roque MM , Goldblatt J , Gustafson JA , Hurtado-Villa P , Johns A , Karp N , Laing NG , Magee L , University of Washington Center for Mendelian Genomics , Mullegama SV , Pachajoa H , Porras-Hurtado GL , Schnur RE , Slee J , Singer SL , Staffenberg DA , Timms AE , Wise CA , Zarante I , Saint-Jeannet JP , Luquetti DV .


Abstract
Craniofacial microsomia (CFM) is the second most common congenital facial anomaly, yet its genetic etiology remains unknown. We perform whole-exome or genome sequencing of 146 kindreds with sporadic (n = 138) or familial (n = 8) CFM, identifying a highly significant burden of loss of function variants in SF3B2 (P = 3.8 × 10-10), a component of the U2 small nuclear ribonucleoprotein complex, in probands. We describe twenty individuals from seven kindreds harboring de novo or transmitted haploinsufficient variants in SF3B2. Probands display mandibular hypoplasia, microtia, facial and preauricular tags, epibulbar dermoids, lateral oral clefts in addition to skeletal and cardiac abnormalities. Targeted morpholino knockdown of SF3B2 in Xenopus results in disruption of cranial neural crest precursor formation and subsequent craniofacial cartilage defects, supporting a link between spliceosome mutations and impaired neural crest development in congenital craniofacial disease. The results establish haploinsufficient variants in SF3B2 as the most prevalent genetic cause of CFM, explaining ~3% of sporadic and ~25% of familial cases.

PubMed ID: 34344887
Article link: Nat Commun
Grant support: [+]

Species referenced: Xenopus laevis

References [+] :
Aoki, Sox10 regulates the development of neural crest-derived melanocytes in Xenopus. 2003, Pubmed, Xenbase