Counteracting epigenetic mechanisms regulate the structural development of neuronal circuitry in human neurons.
Seonhye CheonAllison M CulverAnna M BagnellFoster D RitchieJanay M VacharasinMikayla M McCordCarin M PapendorpEvelyn ChukwurahAustin J SmithMara H CowenTrevor A MorelandPankaj S GhateShannon W DavisJudy S LiuSofia B LizarragaPublished in: Molecular psychiatry (2022)
Autism spectrum disorders (ASD) are associated with defects in neuronal connectivity and are highly heritable. Genetic findings suggest that there is an overrepresentation of chromatin regulatory genes among the genes associated with ASD. ASH1 like histone lysine methyltransferase (ASH1L) was identified as a major risk factor for ASD. ASH1L methylates Histone H3 on Lysine 36, which is proposed to result primarily in transcriptional activation. However, how mutations in ASH1L lead to deficits in neuronal connectivity associated with ASD pathogenesis is not known. We report that ASH1L regulates neuronal morphogenesis by counteracting the catalytic activity of Polycomb Repressive complex 2 group (PRC2) in stem cell-derived human neurons. Depletion of ASH1L decreases neurite outgrowth and decreases expression of the gene encoding the neurotrophin receptor TrkB whose signaling pathway is linked to neuronal morphogenesis. The neuronal morphogenesis defect is overcome by inhibition of PRC2 activity, indicating that a balance between the Trithorax group protein ASH1L and PRC2 activity determines neuronal morphology. Thus, our work suggests that ASH1L may epigenetically regulate neuronal morphogenesis by modulating pathways like the BDNF-TrkB signaling pathway. Defects in neuronal morphogenesis could potentially impair the establishment of neuronal connections which could contribute to the neurodevelopmental pathogenesis associated with ASD in patients with ASH1L mutations.
Keyphrases
- autism spectrum disorder
- municipal solid waste
- sewage sludge
- signaling pathway
- cerebral ischemia
- attention deficit hyperactivity disorder
- genome wide
- gene expression
- intellectual disability
- endothelial cells
- dna methylation
- transcription factor
- risk assessment
- brain injury
- copy number
- dna damage
- spinal cord injury
- oxidative stress
- multiple sclerosis
- cell proliferation
- pi k akt
- amino acid
- long non coding rna
- induced pluripotent stem cells
- protein protein
- pluripotent stem cells