4.7 Article

Epigenomic enhancer annotation reveals a key role for NFIX in neural stem cell quiescence

Journal

GENES & DEVELOPMENT
Volume 27, Issue 16, Pages 1769-1786

Publisher

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.216804.113

Keywords

epigenetics; genomics; NFIX; neural stem cells; nuclear factor one; quiescence; transcription factor

Funding

  1. European Commission [FP7-223210]
  2. Medical Research Council [U117570528]
  3. MRC [G0900491, MC_U117570528] Funding Source: UKRI
  4. Medical Research Council [G0900491, MC_U117570528] Funding Source: researchfish

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The majority of neural stem cells (NSCs) in the adult brain are quiescent, and this fraction increases with aging. Although signaling pathways that promote NSC quiescence have been identified, the transcriptional mechanisms involved are mostly unknown, largely due to lack of a cell culture model. In this study, we first demonstrate that NSC cultures (NS cells) exposed to BMP4 acquire cellular and transcriptional characteristics of quiescent cells. We then use epigenomic profiling to identify enhancers associated with the quiescent NS cell state. Motif enrichment analysis of these enhancers predicts a major role for the nuclear factor one (NFI) family in the gene regulatory network controlling NS cell quiescence. Interestingly, we found that the family member NFIX is robustly induced when NS cells enter quiescence. Using genome-wide location analysis and overexpression and silencing experiments, we demonstrate that NFIX has a major role in the induction of quiescence in cultured NSCs. Transcript profiling of NS cells overexpressing or silenced for Nfix and the phenotypic analysis of the hippocampus of Nfix mutant mice suggest that NFIX controls the quiescent state by regulating the interactions of NSCs with their microenvironment.

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