Contribution of spurious transcription to intellectual disability disorders.
Marilyn ScandagliaÁngel BarcoPublished in: Journal of medical genetics (2019)
During the development of multicellular organisms, chromatin-modifying enzymes orchestrate the establishment of gene expression programmes that characterise each differentiated cell type. These enzymes also contribute to the maintenance of cell type-specific transcription profiles throughout life. But what happens when epigenomic regulation goes awry? Genomic screens in experimental models of intellectual disability disorders (IDDs) caused by mutations in epigenetic machinery-encoding genes have shown that transcriptional dysregulation constitutes a hallmark of these conditions. Here, we underscore the connections between a subset of chromatin-linked IDDs and spurious transcription in brain cells. We also propose that aberrant gene expression in neurons, including both the ectopic transcription of non-neuronal genes and the activation of cryptic promoters, may importantly contribute to the pathoaetiology of these disorders.
Keyphrases
- intellectual disability
- gene expression
- transcription factor
- genome wide
- dna methylation
- autism spectrum disorder
- genome wide identification
- induced apoptosis
- copy number
- dna damage
- spinal cord
- high throughput
- multiple sclerosis
- white matter
- gram negative
- signaling pathway
- genome wide analysis
- brain injury
- endoplasmic reticulum stress
- heat shock protein
- cell proliferation