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. 2024 Mar 1;137(5):jcs261789.
doi: 10.1242/jcs.261789. Epub 2024 Mar 11.

The Drosophila neuroblast polarity cycle at a glance

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The Drosophila neuroblast polarity cycle at a glance

Rhiannon R Penkert et al. J Cell Sci. .

Abstract

Drosophila neural stem cells, or neuroblasts, rapidly proliferate during embryonic and larval development to populate the central nervous system. Neuroblasts divide asymmetrically to create cellular diversity, with each division producing one sibling cell that retains the neuroblast fate and another that differentiates into glia or neurons. This asymmetric outcome is mediated by the transient polarization of numerous factors to the cell cortex during mitosis. The powerful genetics and outstanding imaging tractability of the neuroblast make it an excellent model system for studying the mechanisms of cell polarity. This Cell Science at a Glance article and the accompanying poster explore the phases of the neuroblast polarity cycle and the regulatory circuits that control them. We discuss the key features of the cycle - the targeted recruitment of proteins to specific regions of the plasma membrane and multiple phases of highly dynamic actomyosin-dependent cortical flows that pattern both protein distribution and membrane structure.

Keywords: Drosophila; Asymmetric cell division; Cell cycle; Cell polarity; Neuroblast; Stem cell.

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Conflict of interest statement

Competing interests The authors declare no competing or financial interests.

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See Supplementary information for a high-resolution version of the poster.

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References

    1. Abeysundara, N., Simmonds, A. J. and Hughes, S. C. (2018). Moesin is involved in polarity maintenance and cortical remodeling during asymmetric cell division. Mol. Biol. Cell 29, 419-434. 10.1091/mbc.E17-05-0294 - DOI - PMC - PubMed
    1. Atwood, S. X. and Prehoda, K. E. (2009). aPKC phosphorylates Miranda to polarize fate determinants during neuroblast asymmetric cell division. Curr. Biol. 19, 723-729. 10.1016/j.cub.2009.03.056 - DOI - PMC - PubMed
    1. Atwood, S. X., Chabu, C., Penkert, R. R., Doe, C. Q. and Prehoda, K. E. (2007). Cdc42 acts downstream of Bazooka to regulate neuroblast polarity through Par-6 aPKC. J. Cell Sci. 120, 3200-3206. 10.1242/jcs.014902 - DOI - PMC - PubMed
    1. Bailey, M. J. and Prehoda, K. E. (2015). Establishment of Par-polarized cortical domains via phosphoregulated membrane motifs. Dev. Cell 35, 199-210. 10.1016/j.devcel.2015.09.016 - DOI - PMC - PubMed
    1. Barros, C. S., Phelps, C. B. and Brand, A. H. (2003). Drosophila nonmuscle myosin II promotes the asymmetric segregation of cell fate determinants by cortical exclusion rather than active transport. Dev. Cell 5, 829-840. 10.1016/S1534-5807(03)00359-9 - DOI - PubMed

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