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EP300-ZNF384融合基因产物上调GATA3基因表达,并在B细胞前体急性淋巴细胞白血病细胞中诱导造血干细胞基因表达特征。

EP300-ZNF384 fusion gene product up-regulates GATA3 gene expression and induces hematopoietic stem cell gene expression signature in B-cell precursor acute lymphoblastic leukemia cells.

作者信息

Yaguchi Akinori, Ishibashi Takeshi, Terada Kazuki, Ueno-Yokohata Hitomi, Saito Yuya, Fujimura Junya, Shimizu Toshiaki, Ohki Kentaro, Manabe Atsushi, Kiyokawa Nobutaka

机构信息

Department of Pediatric Hematology and Oncology Research, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo, 157-8535, Japan.

Department of Pediatrics and Adolescent Medicine, Juntendo University Graduate School of Medicine, 3-1-3 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan.

出版信息

Int J Hematol. 2017 Aug;106(2):269-281. doi: 10.1007/s12185-017-2220-6. Epub 2017 Apr 4.

Abstract

ZNF384-related fusion genes are associated with a distinct subgroup of B-cell precursor acute lymphoblastic leukemias in childhood, with a frequency of approximately 3-4%. We previously identified a novel EP300-ZNF384 fusion gene. Patients with the ZNF384-related fusion gene exhibit a hematopoietic stem cell (HSC) gene expression signature and characteristic immunophenotype with negative or low expression of CD10 and aberrant expression of myeloid antigens, such as CD33 and CD13. However, the molecular basis of this pathogenesis remains completely unknown. In the present study, we examined the biological effects of EP300-ZNF384 expression induced by retrovirus-mediated gene transduction in an REH B-cell precursor acute lymphoblastic leukemia cell line, and observed the acquisition of the HSC gene expression signature and an up-regulation of GATA3 gene expression, as assessed by microarray analysis. In contrast, the gene expression profile induced by wild-type ZNF384 in REH cells was significantly different from that by EP300-ZNF384 expression. Together with the results of reporter assays, which revealed the enhancement of GATA3-promoter activity by EP300-ZNF384 expression, these findings suggest that EP300-ZNF384 mediates GATA3 gene expression and may be involved in the acquisition of the HSC gene expression signature and characteristic immunophenotype in B-cell precursor acute lymphoblastic leukemia cells.

摘要

ZNF384相关融合基因与儿童B细胞前体急性淋巴细胞白血病的一个独特亚组相关,频率约为3%-4%。我们之前鉴定出一种新型的EP300-ZNF384融合基因。携带ZNF384相关融合基因的患者表现出造血干细胞(HSC)基因表达特征以及特征性免疫表型,即CD10表达阴性或低表达,以及髓系抗原如CD33和CD13的异常表达。然而,这种发病机制的分子基础仍然完全未知。在本研究中,我们通过逆转录病毒介导的基因转导在REH B细胞前体急性淋巴细胞白血病细胞系中检测了EP300-ZNF384表达的生物学效应,并通过微阵列分析观察到获得了HSC基因表达特征以及GATA3基因表达上调。相比之下,野生型ZNF384在REH细胞中诱导的基因表达谱与EP300-ZNF384表达诱导的基因表达谱显著不同。结合报告基因检测结果(该结果显示EP300-ZNF384表达增强了GATA3启动子活性),这些发现表明EP300-ZNF384介导GATA3基因表达,并且可能参与了B细胞前体急性淋巴细胞白血病细胞中HSC基因表达特征和特征性免疫表型的获得。

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