Department of Dermatology and Venereology, University Hospital of Cologne, Cologne, Germany.
The Cologne Cluster of Excellence in Cellular Stress Responses in Aging-associated Diseases (CECAD), University of Cologne, Cologne, Germany.
EMBO Rep. 2021 Feb 3;22(2):e51127. doi: 10.15252/embr.202051127. Epub 2021 Jan 7.
Centrosomes, composed of two centrioles and pericentriolar material, organize mitotic spindles during cell division and template cilia during interphase. The first few divisions during mouse development occur without centrioles, which form around embryonic day (E) 3. However, disruption of centriole biogenesis in Sas-4 null mice leads to embryonic arrest around E9. Centriole loss in Sas-4 embryos causes prolonged mitosis and p53-dependent cell death. Studies in vitro discovered a similar USP28-, 53BP1-, and p53-dependent mitotic surveillance pathway that leads to cell cycle arrest. In this study, we show that an analogous pathway is conserved in vivo where 53BP1 and USP28 are upstream of p53 in Sas-4 embryos. The data indicate that the pathway is established around E7 of development, four days after the centrioles appear. Our data suggest that the newly formed centrioles gradually mature to participate in mitosis and cilia formation around the beginning of gastrulation, coinciding with the activation of mitotic surveillance pathway upon centriole loss.
中心体由两个中心粒和中心粒周围物质组成,在细胞分裂过程中组织有丝分裂纺锤体,在细胞间期组织纤毛。在小鼠发育的最初几次分裂中没有中心粒,中心粒在胚胎第 3 天左右形成。然而,Sas-4 基因缺失的小鼠中中心粒发生缺陷会导致胚胎在 E9 左右停止发育。Sas-4 胚胎中的中心粒丢失会导致有丝分裂时间延长和 p53 依赖性细胞死亡。体外研究发现了一种类似的 USP28、53BP1 和 p53 依赖性有丝分裂监测途径,可导致细胞周期停滞。在这项研究中,我们表明在体内存在类似的途径,其中 53BP1 和 USP28 在 Sas-4 胚胎中是 p53 的上游。数据表明该途径在发育的 E7 时建立,即在中心粒出现四天后。我们的数据表明,新形成的中心粒逐渐成熟,参与有丝分裂和纤毛形成,大约在原肠胚形成开始时,与中心粒丢失后有丝分裂监测途径的激活相吻合。