Gasiorek Jadwiga J, Blank Volker
Lady Davis Institute for Medical Research, McGill University, 3755 Chemin de la Côte Sainte-Catherine, Montreal, QC, H3T 1E2, Canada.
Cell Mol Life Sci. 2015 Jun;72(12):2323-35. doi: 10.1007/s00018-015-1866-6. Epub 2015 Feb 27.
The NFE2 transcription factor was identified over 25 years ago. The NFE2 protein forms heterodimers with small MAF proteins, and the resulting complex binds to regulatory elements in a large number of target genes. In contrast to other CNC transcription family members including NFE2L1 (NRF1), NFE2L2 (NRF2) and NFE2L3 (NRF3), which are widely expressed, earlier studies had suggested that the major sites of NFE2 expression are hematopoietic cells. Based on cell culture studies it was proposed that this protein acts as a critical regulator of globin gene expression. However, the knockout mouse model displayed only mild erythroid abnormalities, while the major phenotype was a defect in megakaryocyte biogenesis. Indeed, absence of NFE2 led to severely impaired platelet production. A series of recent data, also summarized here, shed new light on the various functional roles of NFE2 and the regulation of its activity. NFE2 is part of a complex regulatory network, including transcription factors such as GATA1 and RUNX1, controlling megakaryocytic and/or erythroid cell function. Surprisingly, it was recently found that NFE2 also has a role in non-hematopoietic tissues, such as the trophoblast, in which it is also expressed, as well as the bone, opening the door to new research areas for this transcription factor. Additional data showed that NFE2 function is controlled by a series of posttranslational modifications. Important strides have been made with respect to the clinical significance of NFE2, linking this transcription factor to hematological disorders such as polycythemias.
NFE2转录因子是在25多年前被鉴定出来的。NFE2蛋白与小MAF蛋白形成异二聚体,形成的复合物与大量靶基因中的调控元件结合。与包括NFE2L1(NRF1)、NFE2L2(NRF2)和NFE2L3(NRF3)在内的其他广泛表达的CNC转录家族成员不同,早期研究表明NFE2的主要表达部位是造血细胞。基于细胞培养研究,有人提出这种蛋白是珠蛋白基因表达的关键调节因子。然而,基因敲除小鼠模型仅表现出轻度的红系异常,而主要表型是巨核细胞生成缺陷。事实上,NFE2的缺失导致血小板生成严重受损。本文也总结的一系列最新数据,为NFE2的各种功能作用及其活性调节提供了新的线索。NFE2是一个复杂调控网络的一部分,该网络包括GATA-1和RUNX1等转录因子,控制巨核细胞和/或红系细胞功能。令人惊讶的是,最近发现NFE2在非造血组织中也有作用,如它也表达的滋养层以及骨骼,这为该转录因子开辟了新的研究领域。其他数据表明,NFE2的功能受一系列翻译后修饰的控制。在NFE2的临床意义方面已经取得了重要进展,将这个转录因子与红细胞增多症等血液系统疾病联系起来。