4.7 Article

The Neocortical Progenitor Specification Program Is Established through Combined Modulation of SHH and FGF Signaling

Journal

JOURNAL OF NEUROSCIENCE
Volume 40, Issue 36, Pages 6872-6887

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.2888-19.2020

Keywords

corticogenesis; FGF; lineage fates; neural progenitors; neurogenesis; SHH

Categories

Funding

  1. National Institutes of Health [R01 MH077694, R01 NS118995]
  2. National Institutes of Health/National Cancer Institute [K01CA201068]
  3. American Brain Tumor Association [ARC1800003]
  4. KNRF [2019M3A9H1103702]
  5. National Research Foundation of Korea [2019M3A9H1103702] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Neuronal progenitors in the developing forebrain undergo dynamic competence states to ensure timely generation of specific excitatory and inhibitory neuronal subtypes from distinct neurogenic niches of the dorsal and ventral forebrain, respectively. Here we show evidence of progenitor plasticity when Sonic hedgehog (SHH) signaling is left unmodulated in the embryonic neocortex of the mammalian dorsal forebrain. We found that, at early stages of corticogenesis, loss of Suppressor of Fused (Sufu), a potent inhibitor of SHH signaling, in neocortical progenitors, altered the transcriptomic landscape of male mouse embryos. Ectopic activation of SHH signaling occurred, via degradation of Gli3R, resulting in significant upregulation of fibroblast growth factor 15 (FGF15) gene expression in all E12.5 Sufu-cKO neocortex regardless of sex. Consequently, activation of FGF signaling, and its downstream effector the MAPK signaling, facilitated expression of genes characteristic of ventral forebrain progenitors. Our studies identify the importance of modulating extrinsic niche signals such as SHH and FGF15, to maintain the competency and specification program of neocortical progenitors throughout corticogenesis.

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