Nap1l1 Controls Embryonic Neural Progenitor Cell Proliferation and Differentiation in the Developing Brain
Progenitor
Brain Development
Neural cell
DOI:
10.1016/j.celrep.2018.02.019
Publication Date:
2018-02-27T16:37:57Z
AUTHORS (6)
ABSTRACT
Highlights•Nap1l1 knockdown or knockout causes abnormal embryonic neurogenesis•Nap1l1 depletion induces neuronal dendrites and morphology•Nap1l1 regulates cortical development via regulation of RassF10SummaryThe precise function role nucleosome assembly protein 1-like 1 (Nap1l1) in brain are unclear. Here, we find that Nap1l1 decreases neural progenitor cell (NPC) proliferation premature differentiation during development. A similar deficiency neurogenesis was observed (KO) mice, which were generated using the CRISPR-Cas9 system. RNA sequencing (RNA-seq) analysis indicates Ras-associated domain family member 10 (RassF10) may be downstream target Nap1l1. Furthermore, found RassF10 expression by promoting SETD1A-mediated H3K4 trimethylation at promoter. KO defects rescued overexpression, suggesting controls NPC through RassF10. Our findings reveal an essential for histone chaperone early development.Graphical abstract
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