Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

S. Riazuddin, M. Hussain, A. Razzaq, Z. Iqbal, M. Shahzad, D. L. Polla, Y. Song, E. van Beusekom, A. A. Khan, L. Tomas-Roca, M. Rashid, M. Y. Zahoor, W. M. Wissink-Lindhout, M. A. R. Basra, M. Ansar, Z. Agha, K. van Heeswijk, F. Rasheed, M. Van de Vorst, J. A. VeltmanC. Gilissen, J. Akram, T. Kleefstra, M. Z. Assir, D. Grozeva, K. Carss, F. L. Raymond, T. D. O'Connor, S. A. Riazuddin, S. N. Khan, Z. M. Ahmed, A. P. M. de Brouwer, H. van Bokhoven*, S. Riazuddin*, UK10K

*Corresponding author for this work

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Abstract

Intellectual disability (ID) is a clinically and genetically heterogeneous disorder, affecting 1-3% of the general population. Although research into the genetic causes of ID has recently gained momentum, identification of pathogenic mutations that cause autosomal recessive ID (ARID) has lagged behind, predominantly due to non-availability of sizeable families. Here we present the results of exome sequencing in 121 large consanguineous Pakistani ID families. In 60 families, we identified homozygous or compound heterozygous DNA variants in a single gene, 30 affecting reported ID genes and 30 affecting novel candidate ID genes. Potential pathogenicity of these alleles was supported by co-segregation with the phenotype, low frequency in control populations and the application of stringent bioinformatics analyses. In another eight families segregation of multiple pathogenic variants was observed, affecting 19 genes that were either known or are novel candidates for ID. Transcriptome profiles of normal human brain tissues showed that the novel candidate ID genes formed a network significantly enriched for transcriptional co-expression (P <0.0001) in the frontal cortex during fetal development and in the temporal-parietal and sub-cortex during infancy through adulthood. In addition, proteins encoded by 12 novel ID genes directly interact with previously reported ID proteins in six known pathways essential for cognitive function (P <0.0001). These results suggest that disruptions of temporal parietal and sub-cortical neurogenesis during infancy are critical to the pathophysiology of ID. These findings further expand the existing repertoire of genes involved in ARID, and provide new insights into the molecular mechanisms and the transcriptome map of ID.

Original languageEnglish
Pages (from-to)1604-1614
Number of pages11
JournalMolecular Psychiatry
Volume22
Issue number11
DOIs
Publication statusPublished - Nov 2017

Keywords

  • NONSYNDROMIC MENTAL-RETARDATION
  • DE-NOVO MUTATIONS
  • COGNITIVE DISORDERS
  • METABOLIC CRISES
  • NETWORKS
  • DEAFNESS
  • AUTISM
  • SCHIZOPHRENIA
  • MORTALITY
  • MARRIAGE
  • Correction: Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

    Riazuddin, S., Hussain, M., Razzaq, A., Iqbal, Z., Shahzad, M., Polla, D. L., Song, Y., van Beusekom, E., Khan, A. A., Tomas-Roca, L., Rashid, M., Zahoor, M. Y., Wissink-Lindhout, W. M., Basra, M. A. R., Ansar, M., Agha, Z., van Heeswijk, K., Rasheed, F., Van de Vorst, M., Veltman, J. A., & 15 othersGilissen, C., Akram, J., Kleefstra, T., Assir, M. Z., Grozeva, D., Carss, K., Raymond, F. L., O'Connor, T. D., Riazuddin, S. A., Khan, S. N., Ahmed, Z. M., de Brouwer, A. P. M., van Bokhoven, H., UK10K, U. K. . . K. & UK10K, 1 Nov 2020, In: Molecular Psychiatry. 25, 11, p. 3101-3102 2 p.

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