ausblenden:
Schlagwörter:
Adolescent; Adult; Amino Acid Sequence; Asian Continental Ancestry Group/genetics; Child; Chromosomes, Human, Pair 9; Consanguinity; Female; *Genes, Recessive; Genetic Linkage; Genome-Wide Association Study/methods; Homozygote; Humans; Intellectual Disability/*genetics; Iran; Male; Mannosidases/*genetics/metabolism; Membrane Proteins/*genetics/metabolism; Molecular Sequence Data; *Mutation, Missense; Pakistan; Pedigree; Polymorphism, Single Nucleotide; Protein Structure, Tertiary; Young Adult
Zusammenfassung:
We have used genome-wide genotyping to identify an overlapping homozygosity-by-descent locus on chromosome 9q34.3 (MRT15) in four consanguineous families affected by nonsyndromic autosomal-recessive intellectual disability (NS-ARID) and one in which the patients show additional clinical features. Four of the families are from Pakistan, and one is from Iran. Using a combination of next-generation sequencing and Sanger sequencing, we have identified mutations in the gene MAN1B1, encoding a mannosyl oligosaccharide, alpha 1,2-mannosidase. In one Pakistani family, MR43, a homozygous nonsense mutation (RefSeq number NM_016219.3: c.1418G>A [p.Trp473*]), segregated with intellectual disability and additional dysmorphic features. We also identified the missense mutation c. 1189G>A (p.Glu397Lys; RefSeq number NM_016219.3), which segregates with NS-ARID in three families who come from the same village and probably have shared inheritance. In the Iranian family, the missense mutation c.1000C>T (p.Arg334Cys; RefSeq number NM_016219.3) also segregates with NS-ARID. Both missense mutations are at amino acid residues that are conserved across the animal kingdom, and they either reduce k(cat) by approximately 1300-fold or disrupt stable protein expression in mammalian cells. MAN1B1 is one of the few NS-ARID genes with an elevated mutation frequency in patients with NS-ARID from different populations.
