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bioRxiv · 10.1101/2020.07.29.227603

Cullin3 promotes stem cell progeny differentiation by facilitating aPKC-directed asymmetric Numb localization

Komori, H.·Anhezini, L.·Rives-Quinto, N.·Han, X.·Esrig, A.·Skeath, J. B.·Lee, C.-Y.
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Abstract

Asymmetric segregation of Numb is a conserved mechanism for regulating Notch-mediated binary cell fate decisions; however, the mechanisms controlling Numb segregation remain unclear. Previous studies have proposed an "exclusion" model, suggesting that atypical protein kinase C (aPKC) negatively regulates Numb cortical localization. Here, we report that aPKC kinase activity positively promotes basal cortical Numb localization during asymmetric division of Drosophila neural stem cells (neuroblasts) and that Cullin 3 (Cul3) is required for aPKC-directed basal Numb localization. In numb- or cul3-mutant brains, decreased levels of Numb segregated into neuroblast progeny failed to downregulate Notch, leading to supernumerary neuroblast formation. Increased aPKC kinase activity suppressed supernumerary neuroblast formation by concentrating residual Numb protein at the basal cortex and in neuroblast progeny, whereas decreased aPKC function enhanced the supernumerary neuroblast phenotype by reducing basal Numb levels. We propose that aPKC and Cul3 promote basal Numb localization, which is required to downregulate Notch signaling and promote differentiation in neuroblast progeny.

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Komori, H., Anhezini, L., Rives-Quinto, N., Han, X., Esrig, A., Skeath, J. B., Lee, C.-Y.. 2020-07-29. Cullin3 promotes stem cell progeny differentiation by facilitating aPKC-directed asymmetric Numb localization. https://doi.org/10.1101/2020.07.29.227603

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