Trans effects of chromosome aneuploidies on DNA methylation patterns in human Down syndrome and mouse models

Genome Biol. 2015 Nov 25:16:263. doi: 10.1186/s13059-015-0827-6.

Abstract

Background: Trisomy 21 causes Down syndrome (DS), but the mechanisms by which the extra chromosome leads to deficient intellectual and immune function are not well understood.

Results: Here, we profile CpG methylation in DS and control cerebral and cerebellar cortex of adults and cerebrum of fetuses. We purify neuronal and non-neuronal nuclei and T lymphocytes and find biologically relevant genes with DS-specific methylation (DS-DM) in each of these cell types. Some genes show brain-specific DS-DM, while others show stronger DS-DM in T cells. Both 5-methyl-cytosine and 5-hydroxy-methyl-cytosine contribute to the DS-DM. Thirty percent of genes with DS-DM in adult brain cells also show DS-DM in fetal brains, indicating early onset of these epigenetic changes, and we find early maturation of methylation patterns in DS brain and lymphocytes. Some, but not all, of the DS-DM genes show differential expression. DS-DM preferentially affected CpGs in or near specific transcription factor binding sites (TFBSs), implicating a mechanism involving altered TFBS occupancy. Methyl-seq of brain DNA from mouse models with sub-chromosomal duplications mimicking DS reveals partial but significant overlaps with human DS-DM and shows that multiple chromosome 21 genes contribute to the downstream epigenetic effects.

Conclusions: These data point to novel biological mechanisms in DS and have general implications for trans effects of chromosomal duplications and aneuploidies on epigenetic patterning.

Publication types

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

MeSH terms

  • Adult
  • Aneuploidy*
  • Animals
  • Brain / growth & development
  • Brain / metabolism*
  • Brain / pathology
  • Chromosomes, Human, Pair 21 / genetics
  • CpG Islands / genetics
  • DNA Methylation / genetics*
  • Disease Models, Animal
  • Down Syndrome / genetics*
  • Down Syndrome / pathology
  • Epigenesis, Genetic*
  • Fetus
  • Humans
  • Mice
  • T-Lymphocytes / metabolism
  • T-Lymphocytes / pathology