Lénárt Péter, Bacher Christian P, Daigle Nathalie, Hand Arthur R, Eils Roland, Terasaki Mark, Ellenberg Jan
Gene Expression and Cell Biology/Biophysics Programmes, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, D-69117 Heidelberg, Germany.
Nature. 2005 Aug 11;436(7052):812-8. doi: 10.1038/nature03810. Epub 2005 Jul 13.
Chromosome capture by microtubules is widely accepted as the universal mechanism of spindle assembly in dividing cells. However, the observed length of spindle microtubules and computer simulations of spindle assembly predict that chromosome capture is efficient in small cells, but may fail in cells with large nuclear volumes such as animal oocytes. Here we investigate chromosome congression during the first meiotic division in starfish oocytes. We show that microtubules are not sufficient for capturing chromosomes. Instead, chromosome congression requires actin polymerization. After nuclear envelope breakdown, we observe the formation of a filamentous actin mesh in the nuclear region, and find that contraction of this network delivers chromosomes to the microtubule spindle. We show that this mechanism is essential for preventing chromosome loss and aneuploidy of the egg--a leading cause of pregnancy loss and birth defects in humans.
微管捕获染色体被广泛认为是分裂细胞中纺锤体组装的普遍机制。然而,观察到的纺锤体微管长度以及纺锤体组装的计算机模拟预测,染色体捕获在小细胞中效率较高,但在具有大核体积的细胞(如动物卵母细胞)中可能会失败。在这里,我们研究海星卵母细胞第一次减数分裂期间的染色体汇聚。我们发现微管不足以捕获染色体。相反,染色体汇聚需要肌动蛋白聚合。核膜破裂后,我们观察到核区域形成丝状肌动蛋白网,并发现该网络的收缩将染色体传递到微管纺锤体。我们表明,这种机制对于防止染色体丢失和卵子非整倍体至关重要——非整倍体是人类妊娠丢失和出生缺陷的主要原因。