Pacquelet Anne
CNRS, UMR6290, Rennes, France.
Université de Rennes 1, Institut de Génétique et Développement de Rennes, Rennes, France.
Results Probl Cell Differ. 2017;61:115-140. doi: 10.1007/978-3-319-53150-2_5.
The first division of the one-cell C. elegans embryo has been a fundamental model in deciphering the mechanisms underlying asymmetric cell division. Polarization of the one-cell zygote is induced by a signal from the sperm centrosome and results in the asymmetric distribution of PAR proteins. Multiple mechanisms then maintain PAR polarity until the end of the first division. Once asymmetrically localized, PAR proteins control several essential aspects of asymmetric division, including the position of the mitotic spindle along the polarity axis. Coordination of the spindle and cytokinetic furrow positions is the next essential step to ensure proper asymmetric division. In this chapter, I review the different mechanisms underlying these successive steps of asymmetric division. Work from the last 30 years has revealed the existence of multiple and redundant regulatory pathways which ensure division robustness. Besides the essential role of PAR proteins, this work also emphasizes the importance of both microtubules and actomyosin throughout the different steps of asymmetric division.
单细胞线虫胚胎的第一次分裂一直是解读不对称细胞分裂潜在机制的基础模型。单细胞受精卵的极化由精子中心体发出的信号诱导产生,导致PAR蛋白的不对称分布。随后多种机制维持PAR极性直至第一次分裂结束。PAR蛋白一旦不对称定位,就会控制不对称分裂的几个关键方面,包括有丝分裂纺锤体沿极性轴的位置。纺锤体和胞质分裂沟位置的协调是确保正确不对称分裂的下一个关键步骤。在本章中,我将回顾不对称分裂这些连续步骤背后的不同机制。过去30年的研究揭示了存在多种冗余调节途径,这些途径确保了分裂的稳健性。除了PAR蛋白的关键作用外,这项工作还强调了微管和肌动球蛋白在不对称分裂不同步骤中的重要性。