Waddle J A, Cooper J A, Waterston R H
Department of Genetics, Washington University School of Medicine, St Louis, MO 63110.
Development. 1994 Aug;120(8):2317-28. doi: 10.1242/dev.120.8.2317.
During Caenorhabditis elegans embryogenesis, specific cells in the P1 lineage rotate their duplicated centrosome pair onto the anterior-posterior axis; this rotation is correlated with and necessary for a differential inheritance of cytoplasmic determinants in the daughter cells. Centrosome pair rotation is sensitive to inhibitors of actin and microtubule polymerization and may require microtubule attachment to a specific cortical site. We show that actin and the barbed-end binding protein, capping protein, transiently accumulate at this cortical site, possibly by assembly onto persistent remnants of previous cell divisions. Based on these observations, we propose a model for the molecular basis of centrosome rotation that is consistent with the dependence of rotation on actin filaments and microtubules.
在秀丽隐杆线虫胚胎发育过程中,P1谱系中的特定细胞将其复制的中心体对旋转到前后轴上;这种旋转与子细胞中细胞质决定因子的差异遗传相关且是其必要条件。中心体对的旋转对肌动蛋白和微管聚合抑制剂敏感,可能需要微管附着到特定的皮质位点。我们发现肌动蛋白和带刺末端结合蛋白(帽蛋白)在这个皮质位点短暂积累,可能是通过组装到先前细胞分裂的持久残余物上。基于这些观察结果,我们提出了一个中心体旋转分子基础的模型,该模型与旋转对肌动蛋白丝和微管的依赖性一致。