Department of Meiosis, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.
Medical Research Council Laboratory of Molecular Biology, Cambridge CB2 0QH, UK.
Science. 2019 Jun 28;364(6447). doi: 10.1126/science.aat9557.
Mammalian oocytes segregate chromosomes with a microtubule spindle that lacks centrosomes, but the mechanisms by which acentrosomal spindles are organized and function are largely unclear. In this study, we identify a conserved subcellular structure in mammalian oocytes that forms by phase separation. This structure, which we term the liquid-like meiotic spindle domain (LISD), permeates the spindle poles and forms dynamic protrusions that extend well beyond the spindle. The LISD selectively concentrates multiple microtubule regulatory factors and allows them to diffuse rapidly within the spindle volume. Disruption of the LISD via different means disperses these factors and leads to severe spindle assembly defects. Our data suggest a model whereby the LISD promotes meiotic spindle assembly by serving as a reservoir that sequesters and mobilizes microtubule regulatory factors in proximity to spindle microtubules.
哺乳动物卵母细胞通过缺乏中心体的微管纺锤体进行染色体分离,但无中心体纺锤体的组织和功能机制在很大程度上尚不清楚。在这项研究中,我们鉴定了哺乳动物卵母细胞中通过相分离形成的一种保守的亚细胞结构。我们将这个结构称为液态减数分裂纺锤体域(LISD),它渗透到纺锤体两极,并形成动态的突起,远远超出纺锤体。LISD 选择性地浓缩多种微管调节因子,并允许它们在纺锤体体积内快速扩散。通过不同的方式破坏 LISD 会分散这些因子,并导致严重的纺锤体组装缺陷。我们的数据表明,LISD 通过充当一个隔离库,将微管调节因子隔离并动员到靠近纺锤体微管的位置,从而促进减数分裂纺锤体的组装。