Kondo Aiko, Fujiwara Tohru, Okitsu Yoko, Fukuhara Noriko, Onishi Yasushi, Nakamura Yukio, Sawada Kenichi, Harigae Hideo
Department of Hematology and Rheumatology, Tohoku University Graduate School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai, 980-8575, Japan.
Molecular Hematology/Oncology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Int J Hematol. 2016 Apr;103(4):387-95. doi: 10.1007/s12185-016-1968-4. Epub 2016 Mar 11.
The transcription factor GATA-1 plays an essential role in erythroid differentiation. To identify novel GATA-1 target genes, we analyzed a merged ChIP-seq and expression profiling dataset. We identified FAM210B as a putative novel GATA-1 target gene. Study results demonstrated that GATA-1 directly regulates FAM210B expression, presumably by binding to an intronic enhancer region. Both human and murine FAM210B are abundantly expressed in the later stages of erythroblast development. Moreover, the deduced amino acid sequence predicted that FAM210B is a membrane protein, and Western blot analysis demonstrated its mitochondrial localization. Loss-of-function analysis in erythroid cells suggested that FAM210B may be involved in erythroid differentiation. The identification and characterization of FAM210B provides new insights in the study of erythropoiesis and hereditary anemias.
转录因子GATA-1在红细胞分化过程中起着至关重要的作用。为了鉴定新的GATA-1靶基因,我们分析了一个整合的染色质免疫沉淀测序(ChIP-seq)和表达谱数据集。我们将FAM210B鉴定为一个假定的新GATA-1靶基因。研究结果表明,GATA-1可能通过结合内含子增强子区域直接调控FAM210B的表达。人和小鼠的FAM210B在成红细胞发育的后期均大量表达。此外,推导的氨基酸序列预测FAM210B是一种膜蛋白,蛋白质免疫印迹分析证实了其线粒体定位。对红细胞系细胞进行的功能缺失分析表明,FAM210B可能参与红细胞分化。FAM210B的鉴定和特征分析为红细胞生成和遗传性贫血的研究提供了新的见解。