Department of Meiosis, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany; email:
Current affiliation: School of Biochemistry, University of Bristol, Bristol, BS8 1TD, United Kingdom.
Annu Rev Cell Dev Biol. 2018 Oct 6;34:381-403. doi: 10.1146/annurev-cellbio-100616-060553. Epub 2018 Jul 20.
Fertilizable eggs develop from diploid precursor cells termed oocytes. Once every menstrual cycle, an oocyte matures into a fertilizable egg in the ovary. To this end, the oocyte eliminates half of its chromosomes into a small cell termed a polar body. The egg is then released into the Fallopian tube, where it can be fertilized. Upon fertilization, the egg completes the second meiotic division, and the mitotic division of the embryo starts. This review highlights recent work that has shed light on the cytoskeletal structures that drive the meiotic divisions of the oocyte in mammals. In particular, we focus on how mammalian oocytes assemble a microtubule spindle in the absence of centrosomes, how they position the spindle in preparation for polar body extrusion, and how the spindle segregates the chromosomes. We primarily focus on mouse oocytes as a model system but also highlight recent insights from human oocytes.
可受精的卵子由称为卵母细胞的二倍体前体细胞发育而来。在每个月经周期中,卵母细胞在卵巢中成熟为可受精的卵子。为此,卵母细胞将其一半染色体排入一个称为极体的小细胞中。然后,卵子被释放到输卵管中,在那里它可以受精。受精后,卵子完成第二次减数分裂,胚胎的有丝分裂开始。这篇综述强调了最近的工作,这些工作揭示了驱动哺乳动物卵母细胞减数分裂的细胞骨架结构。特别是,我们专注于哺乳动物卵母细胞如何在没有中心体的情况下组装微管纺锤体,它们如何为极体挤出做准备来定位纺锤体,以及纺锤体如何分离染色体。我们主要以小鼠卵母细胞作为模型系统,但也强调了来自人类卵母细胞的最新见解。