Université Paris Cité, CNRS, Institut Jacques Monod, Paris, France.
Methods Mol Biol. 2025;2872:141-156. doi: 10.1007/978-1-0716-4224-5_10.
Maintaining genomic integrity throughout successive cell divisions is essential for the proper development and functioning of organisms. Chromosome alignment and segregation occur on a microtubule-based spindle originating from centrosomes. The molecular and cellular mechanisms involved in accurate chromosome segregation during early embryonic divisions are highly conserved between worms and humans. Therefore, C. elegans serves as a robust model for investigating mitotic cell divisions within a metazoan system. Throughout early embryonic development, filming and tracking successive cell divisions becomes progressively more challenging as the number of cells increases and cell size decreases. To address this challenge, we describe a method for preparing live samples, performing 4D time-lapse imaging, and semi-automated tracking of chromosomes and spindle poles during early mitotic divisions in C. elegans embryos.
在连续的细胞分裂过程中保持基因组完整性对于生物体的正常发育和功能至关重要。染色体的排列和分离发生在由中心体起源的微管为基础的纺锤体上。在早期胚胎分裂过程中,准确分离染色体所涉及的分子和细胞机制在蠕虫和人类之间高度保守。因此,秀丽隐杆线虫是研究后生动物系统有丝分裂细胞分裂的强大模型。在早期胚胎发育过程中,随着细胞数量的增加和细胞体积的减小,拍摄和跟踪连续的细胞分裂变得越来越具有挑战性。为了解决这个挑战,我们描述了一种方法,用于制备活样本、进行 4D 延时成像,并在 C. elegans 胚胎的早期有丝分裂过程中半自动跟踪染色体和纺锤体极。