Department of Hematology, Oncology and Cancer Immunology, Campus Virchow, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Leukemia. 2023 Nov;37(11):2237-2249. doi: 10.1038/s41375-023-02013-9. Epub 2023 Aug 30.
Recent exome-wide studies discovered frequent somatic mutations in the epigenetic modifier ZNF217 in primary mediastinal B cell lymphoma (PMBCL) and related disorders. As functional consequences of ZNF217 alterations remain unknown, we comprehensively evaluated their impact in PMBCL. Targeted sequencing identified genetic lesions affecting ZNF217 in 33% of 157 PMBCL patients. Subsequent gene expression profiling (n = 120) revealed changes in cytokine and interferon signal transduction in ZNF217-aberrant PMBCL cases. In vitro, knockout of ZNF217 led to changes in chromatin accessibility interfering with binding motifs for crucial lymphoma-associated transcription factors. This led to disturbed expression of interferon-responsive and inflammation-associated genes, altered cell behavior, and aberrant differentiation. Mass spectrometry demonstrates that ZNF217 acts within a histone modifier complex containing LSD1, CoREST and HDAC and interferes with H3K4 methylation and H3K27 acetylation. Concluding, our data suggest non-catalytic activity of ZNF217, which directs histone modifier complex function and controls B cell differentiation-associated patterns of chromatin structure.
最近的外显子组全基因组研究发现,原发性纵隔 B 细胞淋巴瘤(PMBCL)和相关疾病中存在频繁的表观遗传修饰因子 ZNF217 体细胞突变。由于 ZNF217 改变的功能后果尚不清楚,我们全面评估了它们在 PMBCL 中的影响。靶向测序在 157 例 PMBCL 患者中的 33%中鉴定出影响 ZNF217 的遗传病变。随后的基因表达谱分析(n=120)显示,ZNF217 异常的 PMBCL 病例中细胞因子和干扰素信号转导发生变化。在体外,敲除 ZNF217 导致染色质可及性发生变化,干扰关键淋巴瘤相关转录因子的结合基序。这导致干扰素反应和炎症相关基因的表达失调、细胞行为改变和异常分化。质谱分析表明,ZNF217 在内包含 LSD1、CoREST 和 HDAC 的组蛋白修饰复合物中发挥作用,并干扰 H3K4 甲基化和 H3K27 乙酰化。总之,我们的数据表明 ZNF217 具有非催化活性,可指导组蛋白修饰复合物的功能,并控制 B 细胞分化相关的染色质结构模式。