Phenotypic and molecular convergence of 2q23.1 deletion syndrome with other neurodevelopmental syndromes associated with autism spectrum disorder

Int J Mol Sci. 2015 Apr 7;16(4):7627-43. doi: 10.3390/ijms16047627.

Abstract

Roughly 20% of autism spectrum disorders (ASD) are syndromic with a well-established genetic cause. Studying the genes involved can provide insight into the molecular and cellular mechanisms of ASD. 2q23.1 deletion syndrome (causative gene, MBD5) is a recently identified genetic neurodevelopmental disorder associated with ASD. Mutations in MBD5 have been found in ASD cohorts. In this study, we provide a phenotypic update on the prevalent features of 2q23.1 deletion syndrome, which include severe intellectual disability, seizures, significant speech impairment, sleep disturbance, and autistic-like behavioral problems. Next, we examined the phenotypic, molecular, and network/pathway relationships between nine neurodevelopmental disorders associated with ASD: 2q23.1 deletion Rett, Angelman, Pitt-Hopkins, 2q23.1 duplication, 5q14.3 deletion, Kleefstra, Kabuki make-up, and Smith-Magenis syndromes. We show phenotypic overlaps consisting of intellectual disability, speech delay, seizures, sleep disturbance, hypotonia, and autistic-like behaviors. Molecularly, MBD5 possibly regulates the expression of UBE3A, TCF4, MEF2C, EHMT1 and RAI1. Network analysis reveals that there could be indirect protein interactions, further implicating function for these genes in common pathways. Further, we show that when MBD5 and RAI1 are haploinsufficient, they perturb several common pathways that are linked to neuronal and behavioral development. These findings support further investigations into the molecular and pathway relationships among genes linked to neurodevelopmental disorders and ASD, which will hopefully lead to common points of regulation that may be targeted toward therapeutic intervention.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Autism Spectrum Disorder / genetics
  • Autism Spectrum Disorder / pathology
  • Cells, Cultured
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 2 / genetics*
  • DNA-Binding Proteins / genetics*
  • Female
  • Gene Expression
  • Gene Regulatory Networks
  • Haploinsufficiency
  • Humans
  • Infant
  • Male
  • Neurodevelopmental Disorders / genetics*
  • Neurodevelopmental Disorders / pathology*
  • Signal Transduction
  • Smith-Magenis Syndrome / genetics
  • Smith-Magenis Syndrome / pathology
  • Trans-Activators
  • Transcription Factors / genetics*

Substances

  • DNA-Binding Proteins
  • MBD5 protein, human
  • RAI1 protein, human
  • Trans-Activators
  • Transcription Factors