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Free keywords:
Brain/metabolism/physiology; Cell Cycle; Cognition Disorders/*genetics; Consanguinity; DNA Mutational Analysis; Exons/genetics; Gene Regulatory Networks; Genes, Essential/genetics; Genes, Recessive/*genetics; *High-Throughput Nucleotide Sequencing; Homozygote; Humans; Intellectual Disability/*genetics; Metabolic Networks and Pathways; Mutation/genetics; Organ Specificity; Synapses/metabolism
Abstract:
Common diseases are often complex because they are genetically heterogeneous, with many different genetic defects giving rise to clinically indistinguishable phenotypes. This has been amply documented for early-onset cognitive impairment, or intellectual disability, one of the most complex disorders known and a very important health care problem worldwide. More than 90 different gene defects have been identified for X-chromosome-linked intellectual disability alone, but research into the more frequent autosomal forms of intellectual disability is still in its infancy. To expedite the molecular elucidation of autosomal-recessive intellectual disability, we have now performed homozygosity mapping, exon enrichment and next-generation sequencing in 136 consanguineous families with autosomal-recessive intellectual disability from Iran and elsewhere. This study, the largest published so far, has revealed additional mutations in 23 genes previously implicated in intellectual disability or related neurological disorders, as well as single, probably disease-causing variants in 50 novel candidate genes. Proteins encoded by several of these genes interact directly with products of known intellectual disability genes, and many are involved in fundamental cellular processes such as transcription and translation, cell-cycle control, energy metabolism and fatty-acid synthesis, which seem to be pivotal for normal brain development and function.
