Ge Zheng, Song Evelyn J, Kawasawa Yuka Imamura, Li Jianyong, Dovat Sinisa, Song Chunhua
Department of Hematology (Key Department of Jiangsu Medicine), Zhongda Hospital, Southeast University Medical School, Nanjing, Jiangsu, China.
Department of Pediatrics, Pennsylvania State University College of Medicine, Hershey, PA, USA.
Oncotarget. 2016 Jun 21;7(25):37740-37754. doi: 10.18632/oncotarget.9312.
WD repeat domain 5 (WDR5) plays an important role in various biological functions through the epigenetic regulation of gene transcription. However, the oncogenic effect of WDR5 in leukemia remains largely unknown. Here, we found WDR5 expression is increased in leukemia patients. High expression of WDR5 is associated with high risk leukemia; Patients with WDR5 and MLL1 high expression have poor complete remission rate. We further identified the global genomic binding of WDR5 in leukemic cells and found the genomic co-localization of WDR5 binding with H3K4me3 enrichment. Moreover, WDR5 knockdown by shRNA suppresses cell proliferation, induces apoptosis, inhibits the expression of WDR5 targets, and blocks the H3K4me3 enrichment on the promoter of its targets. We also observed the positive correlation of WDR5 expression with these targets in the cohort study of leukemia patients. Our data reveal that WDR5 may have oncogenic effect and WDR5-mediated H3K4 methylation plays an important role in leukemogenesis.
WD重复结构域5(WDR5)通过基因转录的表观遗传调控在多种生物学功能中发挥重要作用。然而,WDR5在白血病中的致癌作用在很大程度上仍不清楚。在此,我们发现白血病患者中WDR5表达增加。WDR5的高表达与高危白血病相关;WDR5和MLL1高表达的患者完全缓解率较差。我们进一步鉴定了WDR5在白血病细胞中的全基因组结合情况,并发现WDR5结合与H3K4me3富集的基因组共定位。此外,通过shRNA敲低WDR5可抑制细胞增殖、诱导凋亡、抑制WDR5靶标的表达,并阻断其靶标启动子上的H3K4me3富集。在白血病患者的队列研究中,我们还观察到WDR5表达与这些靶标呈正相关。我们的数据表明,WDR5可能具有致癌作用,且WDR5介导的H3K4甲基化在白血病发生中起重要作用。