Marescal Océane, Cheeseman Iain M
Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.
Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.
Cell Rep. 2025 Jul 23;44(8):116041. doi: 10.1016/j.celrep.2025.116041.
During regulated protein degradation, the 26S proteasome recognizes ubiquitinated substrates through its 19S particle and then degrades them in its 20S enzymatic core. Despite this close interdependency between proteasome subunits, we demonstrate that knockouts from different proteasome subcomplexes result in distinct cellular phenotypes. In particular, depletion of 19S PSMD lid proteins, but not that of other proteasome subunits, prevents bipolar spindle assembly during mitosis. Despite decreased ubiquitin-mediated protein degradation in PSMD knockouts, we find that the monopolar spindle phenotype is instead caused by the aberrant degradation of the kinesin motor protein KIF11. We show that KIF11 degradation occurs through the 20S proteasome in a ubiquitin-independent manner upon loss of 19S proteins and that the resulting alterations in spindle forces lead to the unique monopolar phenotype. Thus, the presence of the 19S particle ensures proper spindle formation by restraining ubiquitin-independent degradation.
在受调控的蛋白质降解过程中,26S蛋白酶体通过其19S颗粒识别泛素化底物,然后在其20S酶核心中对其进行降解。尽管蛋白酶体亚基之间存在这种紧密的相互依赖性,但我们证明,来自不同蛋白酶体亚复合物的基因敲除会导致不同的细胞表型。特别是,19S PSMD盖子蛋白的缺失,而不是其他蛋白酶体亚基的缺失,会阻止有丝分裂期间双极纺锤体的组装。尽管在PSMD基因敲除中泛素介导的蛋白质降解减少,但我们发现单极纺锤体表型反而由驱动蛋白KIF11的异常降解引起。我们表明,在19S蛋白缺失时,KIF11通过20S蛋白酶体以不依赖泛素的方式发生降解,并且纺锤体力量的由此产生的改变导致独特的单极表型。因此,19S颗粒的存在通过抑制不依赖泛素的降解来确保纺锤体的正确形成。