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本文引用的文献

1
Differential role for c-Rel and C/EBPbeta/delta in TLR-mediated induction of proinflammatory cytokines.c-Rel与C/EBPβ/δ在Toll样受体介导的促炎细胞因子诱导中的差异作用
J Immunol. 2009 Jun 1;182(11):7212-21. doi: 10.4049/jimmunol.0802971.
2
Linking DNA methylation and histone modification: patterns and paradigms.DNA甲基化与组蛋白修饰的关联:模式与范例
Nat Rev Genet. 2009 May;10(5):295-304. doi: 10.1038/nrg2540.
3
Regulation and function of NF-kappaB transcription factors in the immune system.NF-κB转录因子在免疫系统中的调控与功能
Annu Rev Immunol. 2009;27:693-733. doi: 10.1146/annurev.immunol.021908.132641.
4
A dimer-specific function of the transcription factor NFATp.转录因子NFATp的二聚体特异性功能。
Proc Natl Acad Sci U S A. 2008 Dec 16;105(50):19637-42. doi: 10.1073/pnas.0810648105. Epub 2008 Dec 5.
5
Cytokine and cytokine receptor gene polymorphisms and their functionality.细胞因子和细胞因子受体基因多态性及其功能
Cytokine Growth Factor Rev. 2009 Feb;20(1):43-59. doi: 10.1016/j.cytogfr.2008.11.006. Epub 2008 Nov 28.
6
G9a and HP1 couple histone and DNA methylation to TNFalpha transcription silencing during endotoxin tolerance.在内毒素耐受过程中,G9a和HP1将组蛋白和DNA甲基化与肿瘤坏死因子α转录沉默联系起来。
J Biol Chem. 2008 Nov 21;283(47):32198-208. doi: 10.1074/jbc.M803446200. Epub 2008 Sep 22.
7
IFN-gamma-induced TNF-alpha expression is regulated by interferon regulatory factors 1 and 8 in mouse macrophages.在小鼠巨噬细胞中,干扰素γ诱导的肿瘤坏死因子α表达受干扰素调节因子1和8调控。
J Immunol. 2008 Oct 1;181(7):4461-70. doi: 10.4049/jimmunol.181.7.4461.
8
TRAF6 specifically contributes to FcepsilonRI-mediated cytokine production but not mast cell degranulation.肿瘤坏死因子受体相关因子6(TRAF6)专门促进由IgE高亲和力受体(FcepsilonRI)介导的细胞因子生成,但不影响肥大细胞脱颗粒。
J Biol Chem. 2008 Nov 14;283(46):32110-8. doi: 10.1074/jbc.M802610200. Epub 2008 Sep 4.
9
TRIF and IRF-3 binding to the TNF promoter results in macrophage TNF dysregulation and steatosis induced by chronic ethanol.TRIF和IRF-3与TNF启动子的结合导致慢性乙醇诱导的巨噬细胞TNF失调和脂肪变性。
J Immunol. 2008 Sep 1;181(5):3049-56. doi: 10.4049/jimmunol.181.5.3049.
10
Chromatin profiling across the human tumour necrosis factor gene locus reveals a complex, cell type-specific landscape with novel regulatory elements.对人类肿瘤坏死因子基因座进行染色质分析,揭示了一个具有新型调控元件的复杂的、细胞类型特异性图谱。
Nucleic Acids Res. 2008 Sep;36(15):4845-62. doi: 10.1093/nar/gkn444. Epub 2008 Jul 24.

肿瘤坏死因子基因的转录调控

Transcriptional control of the TNF gene.

作者信息

Falvo James V, Tsytsykova Alla V, Goldfeld Anne E

机构信息

Immune Disease Institute and Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA.

出版信息

Curr Dir Autoimmun. 2010;11:27-60. doi: 10.1159/000289196. Epub 2010 Feb 18.

DOI:10.1159/000289196
PMID:20173386
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4785889/
Abstract

The cytokine TNF is a critical mediator of immune and inflammatory responses. The TNF gene is an immediate early gene, rapidly transcribed in a variety of cell types following exposure to a broad range of pathogens and signals of inflammation and stress. Regulation of TNF gene expression at the transcriptional level is cell type- and stimulus-specific, involving the recruitment of distinct sets of transcription factors to a compact and modular promoter region. In this review, we describe our current understanding of the mechanisms through which TNF transcription is specifically activated by a variety of extracellular stimuli in multiple cell types, including T cells, B cells, macrophages, mast cells, dendritic cells, and fibroblasts. We discuss the role of nuclear factor of activated T cells and other transcription factors and coactivators in enhanceosome formation, as well as the contradictory evidence for a role for nuclear factor kappaB as a classical activator of the TNF gene. We describe the impact of evolutionarily conserved cis-regulatory DNA motifs in the TNF locus upon TNF gene transcription, in contrast to the neutral effect of single nucleotide polymorphisms. We also assess the regulatory role of chromatin organization, epigenetic modifications, and long-range chromosomal interactions at the TNF locus.

摘要

细胞因子TNF是免疫和炎症反应的关键介质。TNF基因是一个即时早期基因,在暴露于多种病原体以及炎症和应激信号后,能在多种细胞类型中迅速转录。TNF基因在转录水平的表达调控具有细胞类型和刺激特异性,涉及将不同的转录因子募集到一个紧凑的模块化启动子区域。在本综述中,我们阐述了目前对多种细胞类型(包括T细胞、B细胞、巨噬细胞、肥大细胞、树突状细胞和成纤维细胞)中多种细胞外刺激特异性激活TNF转录机制的理解。我们讨论了活化T细胞核因子及其他转录因子和共激活因子在增强体形成中的作用,以及核因子κB作为TNF基因经典激活剂作用的矛盾证据。与单核苷酸多态性的中性作用相反,我们描述了TNF基因座中进化保守的顺式调控DNA基序对TNF基因转录的影响。我们还评估了TNF基因座处染色质组织、表观遗传修饰和长程染色体相互作用的调控作用。