Identification of Intellectual Disability Genes in Female Patients with a Skewed X-Inactivation Pattern.

TitleIdentification of Intellectual Disability Genes in Female Patients with a Skewed X-Inactivation Pattern.
Publication TypeJournal Article
Year of Publication2016
AuthorsFieremans, N, Van Esch, H, Holvoet, M, Van Goethem, G, Devriendt, K, Rosello, M, Mayo, S, Martinez, F, Jhangiani, S, Muzny, DM, Gibbs, RA, Lupski, JR, Vermeesch, JR, Marynen, P, Froyen, G
JournalHum Mutat
Date Published2016 Aug
KeywordsCarrier Proteins, Cell Cycle Proteins, Chromosomal Proteins, Non-Histone, DEAD-box RNA Helicases, Exome, Female, Genetic Variation, Humans, Intellectual Disability, Membrane Proteins, Methyl-CpG-Binding Protein 2, Nuclear Proteins, Sequence Analysis, DNA, X Chromosome Inactivation

Intellectual disability (ID) is a heterogeneous disorder with an unknown molecular etiology in many cases. Previously, X-linked ID (XLID) studies focused on males because of the hemizygous state of their X chromosome. Carrier females are generally unaffected because of the presence of a second normal allele, or inactivation of the mutant X chromosome in most of their cells (skewing). However, in female ID patients, we hypothesized that the presence of skewing of X-inactivation would be an indicator for an X chromosomal ID cause. We analyzed the X-inactivation patterns of 288 females with ID, and found that 22 (7.6%) had extreme skewing (>90%), which is significantly higher than observed in the general population (3.6%; P = 0.029). Whole-exome sequencing of 19 females with extreme skewing revealed causal variants in six females in the XLID genes DDX3X, NHS, WDR45, MECP2, and SMC1A. Interestingly, variants in genes escaping X-inactivation presumably cause both XLID and skewing of X-inactivation in three of these patients. Moreover, variants likely accounting for skewing only were detected in MED12, HDAC8, and TAF9B. All tested candidate causative variants were de novo events. Hence, extreme skewing is a good indicator for the presence of X-linked variants in female patients.

Alternate JournalHum Mutat
PubMed ID27159028
PubMed Central IDPMC4940233
Grant ListU54 HG006542 / HG / NHGRI NIH HHS / United States
UM1 HG006542 / HG / NHGRI NIH HHS / United States

Similar Publications