| Literature DB >> 29482721 |
Chwee Tat Koe1, Ye Sing Tan1, Max Lönnfors2, Seong Kwon Hur2, Christine Siok Lan Low3, Yingjie Zhang1,4, Pakorn Kanchanawong3,5, Vytas A Bankaitis2, Hongyan Wang1,4,6.
Abstract
A central feature of most stem cells is the ability to self-renew and undergo differentiation via asymmetric division. However, during asymmetric division the role of phosphatidylinositol (PI) lipids and their regulators is not well established. Here, we show that the sole type I PI transfer protein, Vibrator, controls asymmetric division of Drosophilaneural stem cells (NSCs) by physically anchoring myosin II regulatory light chain, Sqh, to the NSC cortex. Depletion of vib or disruption of its lipid binding and transfer activities disrupts NSC polarity. We propose that Vib stimulates PI4KIIIα to promote synthesis of a plasma membrane pool of phosphatidylinositol 4-phosphate [PI(4)P] that, in turn, binds and anchors myosin to the NSC cortex. Remarkably, Sqh also binds to PI(4)P in vitro and both Vib and Sqh mediate plasma membrane localization of PI(4)P in NSCs. Thus, reciprocal regulation between Myosin and PI(4)P likely governs asymmetric division of NSCs.Entities:
Keywords: D. melanogaster; Drosophila; asymmetric division; developmental biology; neuroblast; neuroscience; phosphatidylinositol lipids; stem cells
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Year: 2018 PMID: 29482721 PMCID: PMC5828666 DOI: 10.7554/eLife.33555
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140