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Rothenpieler, J.

Publications and source records attributed to Rothenpieler, J..

2 recordsLinked to original sources

Notch-independent Her6 contributes to control of neural stem cell maintenance by shifting Notch signaling from lateral inhibition towards lateral induction mode

The growing brain faces the challenge to establish neural stem cell (NSC) populations that accomplish both stable NSC maintenance and dynamic generation of progenitors. Lineage-specific scRNA-seq and time series transcriptome analyses upon overexpression of Notch signaling components in the larval zebrafish brain reveal differential contributions of Notch signaling and Notch-independent Her6, a HES1 homolog, to NSC regulation. Notch signaling and Her6 distinctly regulate cell cycle genes to control G0/G1 or G2 exit and promote quiescence. Her6 and Notch activity combined differentially control delta, jagged, lfng and notch3 expression to potentially shift Notch signaling from Delta-driven lateral inhibition to Jagged-Notch3-mediated lateral induction. We propose that Her6 integrates cell-autonomous lineage-based information and lateral induction-mediated non-autonomous self-organization of neural proliferation zones. Her6-dependent lateral induction maintains persistent NSC patches in ventricular compartments with ongoing neurogenesis, and establishes coherent populations of long-term NSCs in active proliferation zones.

developmental biology↗

Parameters for stable Notch-independent Her6 oscillations across a frequency spectrum in neural stem cell populations

Neural proliferation zones drive the major growth phases of the vertebrate brain. Notch signaling and HES/Her transcription factors control neural stem cell (NSC) maintenance and neurogenesis, however the dynamic regulation of neural proliferation zones to sustain growth is not well understood. Notch-independent expression of the zebrafish HES1 homolog her6 in the larval brain is required for NSC maintenance and growth. We generated an mNeonGreen knock-in into the her6 locus and quantified Her6-mNeonGreen oscillations in vivo in distinct NSC populations. Her6 oscillates cell-autonomously across a broader frequency range, unaffected by inhibition of Notch signaling, and robustly reinitiated after experimental perturbations. Mathematical modelling reveals that Her6 oscillations prevail only when both transcript and protein degradation rate constants are equal. These intrinsic control parameters may have evolved to enable the Her6 oscillator to robustly maintain stemness during proliferative phases irrespective of local Notch signaling cues, and to provide for lineage stability while retaining plasticity for lineage progression.

developmental biology↗