Center for Interdisciplinary Research in Biology, Collège de France, PSL Research University, CNRS, Inserm, Paris, France.
Science. 2022 May 20;376(6595):818-823. doi: 10.1126/science.abg2653. Epub 2022 May 19.
In many vertebrate and invertebrate organisms, gametes develop within groups of interconnected cells called germline cysts formed by several rounds of incomplete divisions. We found that loss of the deubiquitinase USP8 gene in can transform incomplete divisions of germline cells into complete divisions. Conversely, overexpression of USP8 in germline stem cells is sufficient for the reverse transformation from complete to incomplete cytokinesis. The ESCRT-III proteins CHMP2B and Shrub/CHMP4 are targets of USP8 deubiquitinating activity. In mutant sister cells, ectopic recruitment of ESCRT proteins at intercellular bridges causes cysts to break apart. A Shrub/CHMP4 variant that cannot be ubiquitinated does not localize at abscission bridges and cannot complete abscission. Our results uncover ubiquitination of ESCRT-III as a major switch between two types of cell division.
在许多脊椎动物和无脊椎动物中,配子在称为生殖质囊的由几轮不完全分裂形成的相互连接的细胞群内发育。我们发现,在 中缺失去泛素化酶 USP8 基因可以将生殖细胞的不完全分裂转化为完全分裂。相反,在生殖干细胞中过表达 USP8 足以使从完全到不完全胞质分裂的反向转化。ESCRT-III 蛋白 CHMP2B 和 Shrub/CHMP4 是 USP8 去泛素化活性的靶标。在 突变的姐妹细胞中,ESCRT 蛋白在细胞间桥处的异位募集导致小泡破裂。不能泛素化的 Shrub/CHMP4 变体不能定位在分裂桥处,也不能完成分裂。我们的研究结果揭示了 ESCRT-III 的泛素化是两种类型细胞分裂之间的主要开关。