Kalidass Manikandan, Jarubula Venkata Ganesh, Ratnikava Maryia, Chandra Jothipriya Ramakrishnan, Le Goff Samuel, Probst Aline V, Esposito Silvia, Grasser Klaus D, Bruckmann Astrid, Gagneux Jérôme F, Prosée Reinier F, Rutten Twan, Schubert Veit, Demidov Dmitri, Lechner Esther, Steiner Florian A, Genschik Pascal, Lermontova Inna
Kinetochore Biology, Department of Breeding Research, Leibniz Institute of Plant Genetics and Crop Plant Research (IPK) OT Gatersleben, Corrensstr 3, Seeland 06466, Germany.
iGReD, Université Clermont Auvergne, CNRS, INSERM, BP 38, Clermont-Ferrand 63001, France.
Plant Cell. 2025 Jul 1;37(7). doi: 10.1093/plcell/koaf164.
Kinetochores are large protein complexes that serve as attachment sites for spindle microtubules, ensuring proper chromosome segregation during cell division. KINETOCHORE NULL2 (αKNL2) is a key kinetochore protein required for the incorporation of the centromeric histone variant CENH3. The precise regulation of αKNL2 levels is crucial, but the molecular mechanisms controlling this process remain largely unexplored. In this study, we demonstrated that the Anaphase-Promoting Complex/Cyclosome (APC/C) mediates the ubiquitin-dependent proteolysis of αKNL2 during mitosis. Our findings revealed that αKNL2 accumulates in the presence of 26S proteasome inhibitors, and our yeast 2-hybrid and proteomic screens showed that proteins from the ubiquitin-proteasome pathway interact with KNL2 in Arabidopsis (Arabidopsis thaliana) and nematode (Caenorhabditis elegans). Arabidopsis αKNL2 directly interacts with Anaphase-Promoting Complex subunit 10 (APC10) and Cell Division Cycle 20.1 (CDC20.1), 2 substrate recognition components of the APC/C. RNAi-mediated depletion of APC/C resulted in the accumulation and mislocalization of endogenous αKNL2. Additionally, mutation or deletion of the D-box1 region, or substitution of residues K336 and K339, impaired αKNL2 degradation. The expression of a proteasome-resistant αKNL2 variant in planta caused severe defects in growth, fertility, and mitotic division. These findings show that APC/CCDC20-mediated degradation of αKNL2 is critical for proper kinetochore function and centromere integrity.
动粒是一种大型蛋白质复合体,作为纺锤体微管的附着位点,确保细胞分裂过程中染色体的正确分离。动粒缺失蛋白2(αKNL2)是着丝粒组蛋白变体CENH3整合所需的关键动粒蛋白。αKNL2水平的精确调控至关重要,但控制这一过程的分子机制在很大程度上仍未被探索。在本研究中,我们证明了后期促进复合体/细胞周期体(APC/C)在有丝分裂期间介导αKNL2的泛素依赖性蛋白水解。我们的研究结果表明,αKNL2在26S蛋白酶体抑制剂存在的情况下积累,我们的酵母双杂交和蛋白质组学筛选表明,泛素-蛋白酶体途径的蛋白质在拟南芥和线虫中与KNL2相互作用。拟南芥αKNL2直接与后期促进复合体亚基10(APC10)和细胞分裂周期蛋白20.1(CDC20.1)相互作用,这是APC/C的2个底物识别成分。RNA干扰介导的APC/C缺失导致内源性αKNL2的积累和错误定位。此外,D-box1区域的突变或缺失,或K336和K339残基的替换,都会损害αKNL2的降解。在植物中表达抗蛋白酶体的αKNL2变体导致生长、育性和有丝分裂严重缺陷。这些发现表明,APC/CCDC20介导的αKNL2降解对于正确的动粒功能和着丝粒完整性至关重要。