4.7 Article

Chromatin domain alterations linked to 3D genome organization in a large cohort of schizophrenia and bipolar disorder brains

Journal

NATURE NEUROSCIENCE
Volume 25, Issue 4, Pages 474-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41593-022-01032-6

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Funding

  1. Scientific Computing at the Icahn School of Medicine at Mount Sinai
  2. NIH [U01DA048279, R01MH106056]
  3. PsychENCODE Consortium [U01MH103339, U01MH103365, U01MH103392, U01MH103340, U01MH103346, R01MH105472, R01MH094714, R01MH105898, R21MH102791, R21MH105881, R21MH103877, P50MH106934]
  4. National Institute of Mental Health-Intramural Research Program [ZIC MH002903]

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In this study, the researchers constructed chromosomal domains and analyzed histone modifications in the prefrontal cortex of schizophrenia and bipolar disorder patients. They found that there is convergence between genetic risk, neuronal function, and three-dimensional genomics in these disorders. Additionally, they discovered dysregulation of regulatory sequences in the brains of these patients, which are organized into chromosomal domains of various sizes.
Girdhar et al. constructed chromosomal domains from prefrontal histone acetylation and methylation maps and discovered, in a large cohort of schizophrenia and bipolar brains, converging alignment by genetic risk, neuronal function and three-dimensional genomics. Chromosomal organization, scaling from the 147-base pair (bp) nucleosome to megabase-ranging domains encompassing multiple transcriptional units, including heritability loci for psychiatric traits, remains largely unexplored in the human brain. In this study, we constructed promoter- and enhancer-enriched nucleosomal histone modification landscapes for adult prefrontal cortex from H3-lysine 27 acetylation and H3-lysine 4 trimethylation profiles, generated from 388 controls and 351 individuals diagnosed with schizophrenia (SCZ) or bipolar disorder (BD) (n = 739). We mapped thousands of cis-regulatory domains (CRDs), revealing fine-grained, 10(4)-10(6)-bp chromosomal organization, firmly integrated into Hi-C topologically associating domain stratification by open/repressive chromosomal environments and nuclear topography. Large clusters of hyper-acetylated CRDs were enriched for SCZ heritability, with prominent representation of regulatory sequences governing fetal development and glutamatergic neuron signaling. Therefore, SCZ and BD brains show coordinated dysregulation of risk-associated regulatory sequences assembled into kilobase- to megabase-scaling chromosomal domains.

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