A missense variant in the nuclear export signal of the FMR1 gene causes intellectual disability

Fragile X syndrome (FXS) is the most common monogenetic cause of intellectual disability and autism spectrum disorders. Mostly, FXS is caused by transcriptional silencing of the FMR1 gene due to a repeat expansion in the 5' UTR, and consequently lack of the protein product FMRP. However, in rare cases FXS is caused by other types of variants in the FMR1 gene. We describe a missense variant in the FMR1 gene, identified through whole-exome sequencing, in a boy with intellectual disability and behavioral problems. The variant is located in the FMRP's nuclear export signal (NES). We performed expression and localization studies of the variant in hair roots and HEK293 cells. Our results show normal expression but significant retention of the FMRP in the cells' nucleus. This finding suggests a possible FMRP reduction at its essential functional sites in the dendrites and the synaptic compartments and possible interference of other cellular processes in the nucleus. Together, this might lead to a FXS phenotype in the boy.

Automated summary

Fragile X syndrome (FXS) is a common monogenetic cause of intellectual disability and autism spectrum disorders, usually resulting from FMR1 gene transcriptional silencing. A missense variant in the FMR1 gene was described in a boy with intellectual disability, leading to significant retention of FMRP in the nucleus, potentially affecting its essential functional sites in dendrites and synaptic compartments.