Chromosome dynamics and spindle microtubule establishment in mouse embryos

被引:4
|
作者
Macaulay, Angus D. [1 ]
Allais, Adelaide [1 ]
FitzHarris, Greg [1 ,2 ]
机构
[1] Ctr Rech Ctr Hosp Univ Montreal, 900 St Denis St, Montreal, PQ H2X 3H8, Canada
[2] Univ Montreal, Dept OBGYN, Montreal, PQ, Canada
来源
FASEB JOURNAL | 2020年 / 34卷 / 06期
基金
加拿大自然科学与工程研究理事会;
关键词
embryo; error correction; mitosis; spindle; AURORA C; SEGREGATION; CENTROSOME; MECHANISMS; MOSAICISM; MTOCS; CONSEQUENCES; ORGANIZATION; INHERITANCE; ANEUPLOIDY;
D O I
10.1096/fj.201902947R
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chromosome segregation errors in mammalian embryos are common and jeopardize embryo health. Here, we perform for the first time 4-Dimensional imaging and tracking of chromosomes and centromeres through each preimplantation mitotic cell division in mouse embryos to define the normal dynamics of chromosome segregation. We show that a microtubule (MT)-dependent inward movement of chromosomes occurs at the time of nuclear envelope breakdown (NEBD), particularly in the earliest cell divisions, to position chromosomes prior to spindle assembly. Establishment of a rudimentary metaphase plate occurs immediately after NEBD, and is followed by a progressive alignment and biorientation of mitotic chromosomes. Stable end-on kinetochore-MT attachments form rapidly and attachment errors are uncommon. Altogether our data describe a rapid and efficient spindle assembly pathway that apparently minimizes the need for canonical MT attachment error correction in normally dividing embryos.
引用
收藏
页码:8057 / 8067
页数:11
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