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Moesin is involved in polarity maintenance and cortical remodeling during asymmetric cell division

机译:Moesin参与在不对称细胞分裂期间的极性维持和皮质重塑

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An intact actomyosin network is essential for anchoring polarity proteins to the cell cortex and maintaining cell size asymmetry during asymmetric cell division of Drosophila neuroblasts (NBs). However, the mechanisms that control changes in actomyosin dynamics during asymmetric cell division remain unclear. We find that the actin-binding protein, Moesin, is essential for NB proliferation and mitotic progression in the developing brain. During metaphase, phosphorylated Moesin (p-Moesin) is enriched at the apical cortex, and loss of Moesin leads to defects in apical polarity maintenance and cortical stability. This asymmetric distribution of p-Moesin is determined by components of the apical polarity complex and Slik kinase. During later stages of mitosis, p-Moesin localization shifts more basally, contributing to asymmetric cortical extension and myosin basal furrow positioning. Our findings reveal Moesin as a novel apical polarity protein that drives cortical remodeling of dividing NBs, which is essential for polarity maintenance and initial establishment of cell size asymmetry.
机译:完整的肌动素网络对于锚固极性蛋白至细胞皮质和维持果蝇(NBS)的不对称细胞分裂期间的细胞尺寸不对称是必需的。然而,在不对称细胞分裂期间控制肌动素动态变化的机制仍不清楚。我们发现肌动蛋白结合蛋白,Moesin,对于显影大脑的Nb增殖和有丝分裂进展至关重要。在中期期间,磷酸化的moesin(p-moesin)在顶端皮层富集,并且Moesin的损失导致顶端极性维持和皮质稳定性的缺陷。 P-Moesin的这种不对称分布由顶端极性复合物和Slik激酶的组分确定。在微调的后期阶段,P-Moesin定位更恰当地变化,有助于不对称皮质延伸和肌素基沟沟定位。我们的研究结果揭示了Moesin作为一种新的顶端极性蛋白,驱动划分NB的皮质重塑,这对于极性维持和初始建立的细胞尺寸不对称是必不可少的。

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