Fan Jiqiang, Li Qiumei, Liang Jiadi, Chen Zhirong, Chen Linqin, Lai Junzhong, Chen Qi
Fujian Key Laboratory of Innate Immune Biology, Biomedical Research Center of South China, Fujian Normal University, Fuzhou, China.
The Cancer Center, Union Hospital, Fujian Medical University, Fuzhou, China.
Front Microbiol. 2023 Jun 15;14:1158777. doi: 10.3389/fmicb.2023.1158777. eCollection 2023.
IFNβ is a single-copy gene without an intron. Under normal circumstances, it shows low or no expression in cells. It is upregulated only when the body needs it or is stimulated. Stimuli bind to the pattern recognition receptors (PRRs) and pass via various signaling pathways to several basic transcriptional regulators, such as IRFs, NF-кB, and AP-1. Subsequently, the transcriptional regulators enter the nucleus and bind to regulatory elements of the IFNβ promoter. After various modifications, the position of the nucleosome is altered and the complex is assembled to activate the IFNβ expression. However, IFNβ regulation involves a complex network. For the study of immunity and diseases, it is important to understand how transcription factors bind to regulatory elements through specific forms, which elements in cells are involved in regulation, what regulation occurs during the assembly of enhancers and transcription complexes, and the possible regulatory mechanisms after transcription. Thus, this review focuses on the various regulatory mechanisms and elements involved in the activation of IFNβ expression. In addition, we discuss the impact of this regulation in biology.
干扰素β是一个无内含子的单拷贝基因。在正常情况下,它在细胞中表达很低或不表达。只有当机体需要或受到刺激时才会上调表达。刺激物与模式识别受体(PRR)结合,并通过各种信号通路传递给几种基本转录调节因子,如干扰素调节因子(IRF)、核因子κB(NF-кB)和激活蛋白-1(AP-1)。随后,转录调节因子进入细胞核并与干扰素β启动子的调控元件结合。经过各种修饰后,核小体的位置发生改变,复合物组装形成以激活干扰素β的表达。然而,干扰素β的调控涉及一个复杂的网络。对于免疫和疾病的研究而言,了解转录因子如何通过特定形式与调控元件结合、细胞中哪些元件参与调控、增强子和转录复合物组装过程中发生了何种调控以及转录后可能的调控机制非常重要。因此,本综述重点关注参与激活干扰素β表达的各种调控机制和元件。此外,我们还讨论了这种调控在生物学中的影响。