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To characterize features associated with de novo mutations affecting SATB2 function in individuals ascertained on the basis of intellectual disability.Twenty previously unreported individuals with 19 different SATB2 mutations (11 loss-of-function and 8 missense variants) were studied. Fibroblasts were used to measure mutant protein production. Subcellular localization and mobility of wild-type and mutant SATB2 were assessed using fluorescently tagged protein.Recurrent clinical features included neurodevelopmental impairment (19/19), absent/near absent speech (16/19), normal somatic growth (17/19), cleft palate (9/19), drooling (12/19), and dental anomalies (8/19). Six of eight missense variants clustered in the first CUT domain. Sibling recurrence due to gonadal mosaicism was seen in one family. A nonsense mutation in the last exon resulted in production of a truncated protein retaining all three DNA-binding domains. SATB2 nuclear mobility was mutation-dependent; p.Arg389Cys in CUT1 increased mobility and both p.Gly515Ser in CUT2 and p.Gln566Lys between CUT2 and HOX reduced mobility. The clinical features in individuals with missense variants were indistinguishable from those with loss of function.SATB2 haploinsufficiency is a common cause of syndromic intellectual disability. When mutant SATB2 protein is produced, the protein appears functionally inactive with a disrupted pattern of chromatin or matrix association.Genet Med advance online publication 02 February 2017.

Original publication

DOI

10.1038/gim.2016.211

Type

Journal article

Journal

Genetics in medicine : official journal of the American College of Medical Genetics

Publication Date

08/2017

Volume

19

Pages

900 - 908

Addresses

MRC Human Genetics Unit, IGMM, University of Edinburgh, Western General Hospital, Edinburgh, UK.

Keywords

UK10K Consortium, Cell Line, Hela Cells, Humans, Matrix Attachment Region Binding Proteins, Transcription Factors, Cohort Studies, Protein Binding, Mutation, Missense, Genetic Association Studies, Haploinsufficiency, Intellectual Disability, Whole Genome Sequencing, Loss of Function Mutation