Whole genome sequencing of a dizygotic twin suggests a role for the serotonin receptor HTR7 in autism spectrum disorder

Am J Med Genet B Neuropsychiatr Genet. 2016 Dec;171(8):1049-1056. doi: 10.1002/ajmg.b.32473. Epub 2016 Jul 6.

Abstract

Whole genome sequencing of a severely affected dizygotic twin with an autism spectrum disorder and intellectual disability revealed a compound heterozygous mutation in the HTR7 gene as the only variation not detected in control databases. Each parent carries one allele of the mutation, which is not present in an unaffected stepsister. The HTR7 gene encodes the 5-HT7 serotonin receptor that is involved in brain development, synaptic transmission, and plasticity. The paternally inherited p.W60C variant is situated at an evolutionary conserved nucleotide and predicted damaging by Polyphen2. A mutation akin to the maternally inherited pV286I mutation has been reported to significantly affect the binding characteristics of the receptor. Therefore, the observed sequence alterations provide a first suggestive link between a genetic abnormality in the HTR7 gene and a neurodevelopmental disorder. © 2016 Wiley Periodicals, Inc.

Keywords: HTR7; autism; dizygotic twin; intellectual disability; serotonin receptor.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Autism Spectrum Disorder / genetics*
  • Autism Spectrum Disorder / metabolism
  • Autistic Disorder / genetics
  • Child
  • Genetic Predisposition to Disease / genetics
  • Humans
  • Male
  • Mutation
  • Receptors, Serotonin / genetics*
  • Receptors, Serotonin / physiology
  • Sequence Analysis, DNA
  • Serotonin / genetics
  • Serotonin / metabolism
  • Twins, Dizygotic / genetics
  • Twins, Dizygotic / psychology

Substances

  • Receptors, Serotonin
  • serotonin 7 receptor
  • Serotonin