CNRS-LIA Hematology and Cancer, Sino-French Research Center for Life Sciences and Genomics, State Key Laboratory of Medical Genomics, Rui-Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China; and.
Equipe Labellisée No. 11 Ligue Nationale Contre le Cancer, Hôpital St. Louis, Université de Paris 7/INSERM/CNRS UMR 944/7212, Paris, France.
FASEB J. 2018 Sep;32(9):4930-4940. doi: 10.1096/fj.201701450RR. Epub 2018 Apr 10.
RING finger protein 4 (RNF4) is a multifunctional small ubiquitin-related modifier (SUMO)-targeted ubiquitin E3 ligase (STUbL) ubiquitously expressed in all tissues, and which mainly participates in DNA repair and in chromatin and transcriptional regulation. Although RNF4 has been implicated in hematopoietic disorders, its ontogenic role during hematopoietic development remains undiscovered. We generated a zebrafish rnf4 knockout line by using transcription activator-like effector nucleases technology to address the impact of rnf4 during hematopoiesis. Rnf4-deficient zebrafish embryos exhibited sharply decreased neutrophils numbers during both primitive and definitive hematopoiesis. Mechanistic studies revealed that repression of the key granulocytic activator, CCAAT/enhancer-binding protein α ( c/ebpα), via promoter hypermethylation by SUMOylated DNA methyltransferase 1 (DNMT1) was the main cause of impaired granulopoiesis in rnf4-deficient zebrafish. In addition, for the first time, we identified DNMT1 as a potential new STUbL substrate of RNF4, with knockdown of dnmt1 largely restoring primitive and definitive granulopoiesis in rnf4-deficient zebrafish. Collectively, RNF4 is indispensable for zebrafish granulopoiesis through regulation of the DNMT1-C/EBPα functional axis.-Wang, L., Liu, X., Wang, H., Yuan, H., Chen, S., Chen, Z., de The, H., Zhou, J., Zhu, J. RNF4 regulates zebrafish granulopoiesis through the DNMT1-C/EBPα axis.
环指蛋白 4(RNF4)是一种多功能的小泛素相关修饰物(SUMO)靶向泛素 E3 连接酶(STUbL),在所有组织中广泛表达,主要参与 DNA 修复以及染色质和转录调控。虽然 RNF4 已被涉及到血液系统疾病,但它在造血发育过程中的个体发生作用仍未被发现。我们利用转录激活因子样效应物核酸酶技术生成了一种斑马鱼 rnf4 敲除系,以解决 rnf4 在造血过程中的影响。Rnf4 缺陷型斑马鱼胚胎在原始和定型造血过程中中性粒细胞数量明显减少。机制研究表明,SUMO 化的 DNA 甲基转移酶 1(DNMT1)通过启动子超甲基化抑制关键粒细胞激活因子 CCAAT/增强子结合蛋白 α(c/ebpα)是 rnf4 缺陷型斑马鱼粒细胞生成受损的主要原因。此外,我们首次鉴定了 DNMT1 是 RNF4 的一个潜在的新 STUbL 底物,dnmt1 的敲低在很大程度上恢复了 rnf4 缺陷型斑马鱼的原始和定型粒细胞生成。总之,RNF4 通过调节 DNMT1-C/EBPα 功能轴对斑马鱼粒细胞生成是不可或缺的。