We found a match
Your institution may have rights to this item. Sign in to continue.
- Title
SNIP1 and PRC2 coordinate cell fates of neural progenitors during brain development.
- Authors
Matsui, Yurika; Djekidel, Mohamed Nadhir; Lindsay, Katherine; Samir, Parimal; Connolly, Nina; Wu, Gang; Yang, Xiaoyang; Fan, Yiping; Xu, Beisi; Peng, Jamy C.
- Abstract
Stem cell survival versus death is a developmentally programmed process essential for morphogenesis, sizing, and quality control of genome integrity and cell fates. Cell death is pervasive during development, but its programming is little known. Here, we report that Smad nuclear interacting protein 1 (SNIP1) promotes neural progenitor cell survival and neurogenesis and is, therefore, integral to brain development. The SNIP1-depleted brain exhibits dysplasia with robust induction of caspase 9-dependent apoptosis. Mechanistically, SNIP1 regulates target genes that promote cell survival and neurogenesis, and its activities are influenced by TGFβ and NFκB signaling pathways. Further, SNIP1 facilitates the genomic occupancy of Polycomb complex PRC2 and instructs H3K27me3 turnover at target genes. Depletion of PRC2 is sufficient to reduce apoptosis and brain dysplasia and to partially restore genetic programs in the SNIP1-depleted brain in vivo. These findings suggest a loci-specific regulation of PRC2 and H3K27 marks to toggle cell survival and death in the developing brain. The balance of stem cell maintenance, differentiation, and programmed death is critical for proper development. Here they show that SNIP1 is critical for stem cell survival and differentiation in the developing brain where it acts downstream of TGFb and NFkB and regulates PRC2 activities for governing cell fates.
- Subjects
NEURAL development; CELL survival; PROGENITOR cells; STEM cells; DEVELOPMENTAL neurobiology; BRAIN death; PROGRAMMED cell death 1 receptors
- Publication
Nature Communications, 2023, Vol 14, Issue 1, p1
- ISSN
2041-1723
- Publication type
Article
- DOI
10.1038/s41467-023-40487-4