Gene expression links functional networks across cortex and striatum

Nat Commun. 2018 Apr 12;9(1):1428. doi: 10.1038/s41467-018-03811-x.

Abstract

The human brain is comprised of a complex web of functional networks that link anatomically distinct regions. However, the biological mechanisms supporting network organization remain elusive, particularly across cortical and subcortical territories with vastly divergent cellular and molecular properties. Here, using human and primate brain transcriptional atlases, we demonstrate that spatial patterns of gene expression show strong correspondence with limbic and somato/motor cortico-striatal functional networks. Network-associated expression is consistent across independent human datasets and evolutionarily conserved in non-human primates. Genes preferentially expressed within the limbic network (encompassing nucleus accumbens, orbital/ventromedial prefrontal cortex, and temporal pole) relate to risk for psychiatric illness, chloride channel complexes, and markers of somatostatin neurons. Somato/motor associated genes are enriched for oligodendrocytes and markers of parvalbumin neurons. These analyses indicate that parallel cortico-striatal processing channels possess dissociable genetic signatures that recapitulate distributed functional networks, and nominate molecular mechanisms supporting cortico-striatal circuitry in health and disease.

Publication types

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

MeSH terms

  • Adult
  • Animals
  • Atlases as Topic
  • Autopsy
  • Biomarkers / metabolism
  • Chloride Channels / genetics
  • Chloride Channels / metabolism
  • Female
  • Gene Expression Profiling
  • Gene Expression*
  • Humans
  • Macaca / anatomy & histology
  • Macaca / metabolism*
  • Male
  • Middle Aged
  • Nerve Net / anatomy & histology
  • Nerve Net / cytology
  • Nerve Net / metabolism*
  • Neural Pathways / anatomy & histology
  • Neural Pathways / cytology
  • Neural Pathways / metabolism
  • Neurons / cytology
  • Neurons / metabolism
  • Nucleus Accumbens / anatomy & histology
  • Nucleus Accumbens / cytology
  • Nucleus Accumbens / metabolism*
  • Oligodendroglia / cytology
  • Oligodendroglia / metabolism
  • Parvalbumins / genetics
  • Parvalbumins / metabolism
  • Prefrontal Cortex / anatomy & histology
  • Prefrontal Cortex / cytology
  • Prefrontal Cortex / metabolism*
  • Somatostatin / genetics
  • Somatostatin / metabolism
  • Temporal Lobe / anatomy & histology
  • Temporal Lobe / cytology
  • Temporal Lobe / metabolism*

Substances

  • Biomarkers
  • Chloride Channels
  • Parvalbumins
  • Somatostatin