Central neurogenetic signatures of the visuomotor integration system

Proc Natl Acad Sci U S A. 2020 Mar 24;117(12):6836-6843. doi: 10.1073/pnas.1912429117. Epub 2020 Mar 6.

Abstract

Visuomotor impairments characterize numerous neurological disorders and neurogenetic syndromes, such as autism spectrum disorder (ASD) and Dravet, Fragile X, Prader-Willi, Turner, and Williams syndromes. Despite recent advances in systems neuroscience, the biological basis underlying visuomotor functional impairments associated with these clinical conditions is poorly understood. In this study, we used neuroimaging connectomic approaches to map the visuomotor integration (VMI) system in the human brain and investigated the topology approximation of the VMI network to the Allen Human Brain Atlas, a whole-brain transcriptome-wide atlas of cortical genetic expression. We found the genetic expression of four genes-TBR1, SCN1A, MAGEL2, and CACNB4-to be prominently associated with visuomotor integrators in the human cortex. TBR1 gene transcripts, an ASD gene whose expression is related to neural development of the cortex and the hippocampus, showed a central spatial allocation within the VMI system. Our findings delineate gene expression traits underlying the VMI system in the human cortex, where specific genes, such as TBR1, are likely to play a central role in its neuronal organization, as well as on specific phenotypes of neurogenetic syndromes.

Keywords: TBR1; brain functional networks; functional connectivity; genetics; visuomotor integration.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Autism Spectrum Disorder / genetics
  • Autism Spectrum Disorder / pathology
  • Brain Mapping
  • Calcium Channels / genetics*
  • Cohort Studies
  • Epilepsies, Myoclonic / genetics
  • Epilepsies, Myoclonic / pathology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Motor Cortex / physiopathology*
  • NAV1.1 Voltage-Gated Sodium Channel / genetics*
  • Neurodevelopmental Disorders / genetics
  • Neurodevelopmental Disorders / pathology*
  • Prader-Willi Syndrome / genetics
  • Prader-Willi Syndrome / pathology
  • Proteins / genetics*
  • Psychomotor Performance
  • T-Box Domain Proteins / genetics*
  • Visual Cortex / physiopathology*
  • Visual Perception

Substances

  • CACNB4 protein, human
  • Calcium Channels
  • MAGEL2 protein, human
  • NAV1.1 Voltage-Gated Sodium Channel
  • Proteins
  • SCN1A protein, human
  • T-Box Domain Proteins
  • TBR1 protein, human