Liu Hui, Zeng Lijie, Wang Chaomeng, Chen Yingying, Li Liyan, Liu Zhaoyun, Wang Honglei, Fu Rong
Department of Hematology, Tianjin Medical University General Hospital, Tianjin, China.
Tianjin Key Laboratory of Bone Marrow Failure and Malignant Hemopoietic Clone Control, Tianjin, China.
J Cell Mol Med. 2025 Jun;29(11):e70597. doi: 10.1111/jcmm.70597.
Secondary gene mutations are one of the main mechanisms underlying paroxysmal nocturnal haemoglobinuria (PNH) clone proliferation. Our previous studies showed that SUZ12 participates in PNH clone proliferation by regulating H3K27me3. However, the mechanism underlying the SUZ12 function remains unclear. Immunoprecipitation and mass spectrometry were used to identify SUZ12 interacting proteins in PIGA-KO K562 cells. Furthermore, RNA-seq was used to explore the signalling pathways. Finally, colony formation assays, western blotting, and flow cytometry were performed to determine the proliferative ability of the cells. We identified 59 potential proteins that interact with SUZ12 and revealed a physical interaction between MIB2 and SUZ12 exclusively in the K562-KO cell line. Furthermore, we emphasise the vital involvement of the MIB/HERC and ZZ-type domains in the physical association between MIB2 and SUZ12. After MIB2 knockdown, SUZ12 protein decreased while the ubiquitination levels of SUZ12 were enhanced. Additionally, PRC2-related target genes were upregulated in the siMIB2 group. SUZ12 and H3K27me3 expression levels and cell proliferation significantly decreased after MIB2 knockdown, whereas cell apoptosis significantly increased. MIB2 protein levels are also elevated in patients with PNH. In conclusion, MIB2 affects the stability of the PRC2 complex by mediating SUZ12 ubiquitination, which in turn regulates PNH clone proliferation.
继发性基因突变是阵发性夜间血红蛋白尿(PNH)克隆增殖的主要机制之一。我们之前的研究表明,SUZ12通过调节H3K27me3参与PNH克隆增殖。然而,SUZ12功能的潜在机制仍不清楚。采用免疫沉淀和质谱法鉴定PIGA-KO K562细胞中与SUZ12相互作用的蛋白质。此外,利用RNA测序探索信号通路。最后,进行集落形成试验、蛋白质免疫印迹和流式细胞术以确定细胞的增殖能力。我们鉴定出59种与SUZ12相互作用的潜在蛋白质,并揭示了MIB2与SUZ12仅在K562-KO细胞系中的物理相互作用。此外,我们强调了MIB/HERC和ZZ型结构域在MIB2与SUZ12物理结合中的重要作用。敲低MIB2后,SUZ12蛋白减少,而SUZ12的泛素化水平增强。此外,PRC2相关靶基因在siMIB2组中上调。敲低MIB2后,SUZ12和H3K27me3的表达水平以及细胞增殖显著降低,而细胞凋亡显著增加。PNH患者的MIB2蛋白水平也升高。总之,MIB2通过介导SUZ12泛素化影响PRC2复合物的稳定性,进而调节PNH克隆增殖。