ASH2L regulates postnatal neurogenesis through Onecut2-mediated inhibition of TGF-β signaling pathway.
Ya-Jie XuShang-Kun DaiChun-Hui DuanZi-Han ZhangPei-Pei LiuCong LiuHong-Zhen DuXu-Kun LuShijun HuLei LiZhao-Qian TengChang-Mei LiuPublished in: Cell death and differentiation (2023)
The ability of neural stem/progenitor cells (NSPCs) to proliferate and differentiate is required through different stages of neurogenesis. Disturbance in the regulation of neurogenesis causes many neurological diseases, such as intellectual disability, autism, and schizophrenia. However, the intrinsic mechanisms of this regulation in neurogenesis remain poorly understood. Here, we report that Ash2l (Absent, small or homeotic discs-like 2), one core component of a multimeric histone methyltransferase complex, is essential for NSPC fate determination during postnatal neurogenesis. Deletion of Ash2l in NSPCs impairs their capacity for proliferation and differentiation, leading to simplified dendritic arbors in adult-born hippocampal neurons and deficits in cognitive abilities. RNA sequencing data reveal that Ash2l primarily regulates cell fate specification and neuron commitment. Furthermore, we identified Onecut2, a major downstream target of ASH2L characterized by bivalent histone modifications, and demonstrated that constitutive expression of Onecut2 restores defective proliferation and differentiation of NSPCs in adult Ash2l-deficient mice. Importantly, we identified that Onecut2 modulates TGF-β signaling in NSPCs and that treatment with a TGF-β inhibitor rectifies the phenotype of Ash2l-deficient NSPCs. Collectively, our findings reveal the ASH2L-Onecut2-TGF-β signaling axis that mediates postnatal neurogenesis to maintain proper forebrain function.
Keyphrases
- municipal solid waste
- sewage sludge
- intellectual disability
- cerebral ischemia
- signaling pathway
- neural stem cells
- cell fate
- transforming growth factor
- autism spectrum disorder
- single cell
- preterm infants
- anaerobic digestion
- poor prognosis
- genome wide
- epithelial mesenchymal transition
- spinal cord
- dna methylation
- traumatic brain injury
- subarachnoid hemorrhage
- pi k akt
- oxidative stress
- blood brain barrier
- risk assessment
- spinal cord injury
- machine learning
- high resolution
- cell proliferation
- artificial intelligence
- preterm birth
- endoplasmic reticulum stress
- solid phase extraction
- deep learning