Spindle tubulin and MTOC asymmetries may explain meiotic drive in oocytes

被引:38
|
作者
Wu, Tianyu [1 ]
Lane, Simon I. R. [1 ,2 ]
Morgan, Stephanie L. [1 ]
Jones, Keith T. [1 ]
机构
[1] Univ Southampton, Fac Nat & Environm Sci, Biol Sci, Southampton SO17 1BJ, Hants, England
[2] Univ Southampton, Inst Life Sci, Southampton SO17 1BJ, Hants, England
来源
NATURE COMMUNICATIONS | 2018年 / 9卷
基金
英国生物技术与生命科学研究理事会;
关键词
KINETOCHORE-MICROTUBULE ATTACHMENTS; AURORA B KINASE; MOUSE OOCYTES; MEIOSIS-I; ASSEMBLY CHECKPOINT; CHROMOSOME SEGREGATION; SYMMETRY-BREAKING; ERROR; ACTIVATION; DYNAMICS;
D O I
10.1038/s41467-018-05338-7
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
In the first meiotic division (MI) of oocytes, the cortically positioned spindle causes bivalent segregation in which only the centre-facing homologue pairs are retained. 'Selfish' chromosomes are known to exist, which bias their spindle orientation and hence retention in the egg, a process known as 'meiotic drive'. Here we report on this phenomenon in oocytes from F-1 hybrid mice, where parental strain differences in centromere size allows distinction of the two homologue pairs of a bivalent. Bivalents with centromere and kinetochore asymmetry show meiotic drive by rotating during prometaphase, in a process dependent on aurora kinase activity. Cortically positioned homologue pairs appear to be under greater stretch than their centre-facing partners. Additionally the cortex spindle-half contain a greater density of tubulin and microtubule organising centres. A model is presented in which meiotic drive is explained by the impact of microtubule force asymmetry on chromosomes with different sized centromeres and kinetochores.
引用
收藏
页数:11
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