Lambert J David, Nagy Lisa M
Department of Molecular and Cellular Biology, University of Arizona, Tucson, Arizona 85721, USA.
Nature. 2002 Dec 12;420(6916):682-6. doi: 10.1038/nature01241.
During development, different cell fates are generated by cell-cell interactions or by the asymmetric distribution of patterning molecules. Asymmetric inheritance is known to occur either through directed transport along actin microfilaments into one daughter cell or through capture of determinants by a region of the cortex inherited by one daughter. Here we report a third mechanism of asymmetric inheritance in a mollusc embryo. Different messenger RNAs associate with centrosomes in different cells and are subsequently distributed asymmetrically during division. The segregated mRNAs are diffusely distributed in the cytoplasm and then localize, in a microtubule-dependent manner, to the pericentriolar matrix. During division, they dissociate from the core mitotic centrosome and move by means of actin filaments to the presumptive animal daughter cell cortex. In experimental cells with two interphase centrosomes, mRNAs accumulate on the correct centrosome, indicating that differences between centrosomes control mRNA targeting. Blocking the accumulation of mRNAs on the centrosome shows that this event is required for subsequent cortical localization. These events produce a complex pattern of mRNA localization, in which different messages distinguish groups of cells with the same birth order rank and similar developmental potentials.
在发育过程中,不同的细胞命运是由细胞间相互作用或模式分子的不对称分布产生的。已知不对称遗传要么通过沿着肌动蛋白微丝向一个子细胞的定向运输发生,要么通过一个子细胞继承的皮质区域捕获决定因素发生。在这里,我们报告了软体动物胚胎中不对称遗传的第三种机制。不同的信使核糖核酸(mRNA)在不同细胞中与中心体结合,随后在细胞分裂期间不对称分布。分离的mRNA在细胞质中呈弥散分布,然后以微管依赖的方式定位于中心粒周围基质。在细胞分裂期间,它们从有丝分裂核心中心体解离,并通过肌动蛋白丝移动到假定的动物子细胞皮质。在具有两个间期中心体的实验细胞中,mRNA在正确的中心体上积累,这表明中心体之间的差异控制mRNA靶向。阻断mRNA在中心体上的积累表明,这一事件是随后皮质定位所必需的。这些事件产生了复杂的mRNA定位模式,其中不同的信息区分了具有相同出生顺序等级和相似发育潜能的细胞群。