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Control of asymmetric cell division

机译:不对称细胞分裂的控制

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Asymmetric cell division (ACD) is a mechanism to generate cellular diversity and used by prokaryotes and eukaryotes alike. Stem cells in particular rely on ACD to self-renew the stem cell while simultaneously generating a differentiating sibling. It is well established that the differential partitioning of cell fate determinants in the form of RNA and proteins between sibling cells induces changes in cell behavior and fate. Recently, insight into molecular mechanisms has been gained that could explain how centrosomes and centrosome-associated structures such as histones, chromosomes or the primary cilium, segregate asymmetrically. Similarly, many cell types also generate physical asymmetry in the form of sibling cell size differences. Emerging data suggests that spindle-induced cleavage furrow positioning through regulated spindle placement and spindle geometry is insufficient to explain all occurrence of cell-size asymmetry. Instead, asymmetric membrane extension based on asymmetric Myosin localization and cortical remodeling could be a driving force for the generation of physical asymmetry.
机译:不对称细胞分裂(ACD)是一种产生细胞多样性的机制,原核生物和真核生物均使用这种机制。特别是干细胞依靠ACD自我更新干细胞,同时产生分化同胞。公认的是,同胞之间以RNA和蛋白质形式存在的细胞命运决定因素的差异分配会引起细胞行为和命运的变化。最近,获得了对分子机制的见解,可以解释中心体和与中心体相关的结构(例如组蛋白,染色体或初级纤毛)如何不对称地分离。同样,许多细胞类型也以同胞大小差异的形式产生物理不对称性。新兴数据表明,通过调控的纺锤体放置和纺锤体几何形状引起的纺锤体诱导的沟裂定位不足以解释所有细胞大小不对称现象。相反,基于不对称肌球蛋白定位和皮层重塑的不对称膜延伸可能是产生物理不对称性的驱动力。

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