Mechanisms of minor pole-mediated spindle bipolarization in human oocytes.
Tianyu WuYuxi LuoMeiling ZhangBiaobang ChenXingzhu DuHao GuSiyuan XieZhiqi PanRan YuRuiqi HaiXiangli NiuGuimin HaoLi-Ping JinJuanzi ShiXiao-Xi SunYanping KuangWen LiQing SangLei WangPublished in: Science (New York, N.Y.) (2024)
Spindle bipolarization, the process of a microtubule mass transforming into a bipolar spindle, is a prerequisite for accurate chromosome segregation. In contrast to mitotic cells, the process and mechanism of spindle bipolarization in human oocytes remains unclear. Using high-resolution imaging in more than 1800 human oocytes, we revealed a typical state of multipolar intermediates that form during spindle bipolarization and elucidated the mechanism underlying this process. We found that the minor poles formed in multiple kinetochore clusters contribute to the generation of multipolar intermediates. We further determined the essential roles of HAUS6, KIF11, and KIF18A in spindle bipolarization and identified mutations in these genes in infertile patients characterized by oocyte or embryo defects. These results provide insights into the physiological and pathological mechanisms of spindle bipolarization in human oocytes.
Keyphrases
- endothelial cells
- high resolution
- induced pluripotent stem cells
- pluripotent stem cells
- end stage renal disease
- metabolic syndrome
- ejection fraction
- magnetic resonance imaging
- gene expression
- chronic kidney disease
- genome wide
- type diabetes
- dna methylation
- peritoneal dialysis
- adipose tissue
- computed tomography
- newly diagnosed
- mass spectrometry
- oxidative stress
- insulin resistance
- transcription factor
- bipolar disorder
- liquid chromatography
- pregnancy outcomes
- fluorescence imaging