A contractile nuclear actin network drives chromosome congression in oocytes

被引:188
作者
Lénárt, P
Bacher, CP
Daigle, N
Hand, AR
Eils, R
Terasaki, M
Ellenberg, J
机构
[1] European Mol Biol Lab, Gene Express & Cell Biol Programme, D-69117 Heidelberg, Germany
[2] European Mol Biol Lab, Biophys Programme, D-69117 Heidelberg, Germany
[3] German Canc Res Ctr, D-69120 Heidelberg, Germany
[4] Univ Connecticut, Ctr Hlth, Dept Orthodont, Farmington, CT 06030 USA
[5] Univ Connecticut, Ctr Hlth, Dept Oral & Maxillofacial Surg, Farmington, CT 06030 USA
[6] Univ Connecticut, Ctr Hlth, Dept Pediat Dent, Farmington, CT 06030 USA
[7] Univ Connecticut, Ctr Hlth, Dept Adv Gen Dent, Farmington, CT 06030 USA
[8] Univ Connecticut, Ctr Hlth, Dept Physiol, Farmington, CT 06030 USA
[9] Marine Biol Lab, Woods Hole, MA 02543 USA
关键词
D O I
10.1038/nature03810
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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收藏
页码:812 / 818
页数:7
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