Revilla Yolanda, Granja Aitor G
Centro de Biologia Molecular "Severo Ochoa," (CSIC-UAM) Universidad Autonoma de Madrid, 28049 Madrid, Spain.
Crit Rev Immunol. 2009;29(2):131-54. doi: 10.1615/critrevimmunol.v29.i2.30.
The transcriptional coactivators CREB-binding protein (capital ES, Cyrilliccapital VE, Cyrilliccapital ER, Cyrillic) and small er, Cyrillic300 regulate inducible transcription in multiple cellular processes and during the establishment of inflammatory and immune response. These closely related transcriptional coactivators arc able to modulate the transcription of specific genes, modify chromatin structure, and influence cell-cycle progression. Several viruses have been shown to interfere with CREB-binding protein/small er, Cyrillic300 function, modulating their transcriptional activity. During a viral infection, reprogramming of the host cell gene expression pattern is required to establish an adequate antiviral response and, thus, many viruses encode proteins that can influence or interfere with cellular signals to evade inflammation and immune response. The mechanism of transcriptional regulation by coactivator proteins, including small er, Cyrillic300/CBP, has been the focus of intense study. As a part of this, some of the molecular instruments developed by viruses to counteract the host response and their role in the regulation of inflammation and immune response are summarized in this review.
转录共激活因子 CREB 结合蛋白(大写的 ES,西里尔文大写的 VE,西里尔文大写的 ER,西里尔文)和小 e,西里尔文 300 在多种细胞过程以及炎症和免疫反应建立期间调节诱导性转录。这些密切相关的转录共激活因子能够调节特定基因的转录、改变染色质结构并影响细胞周期进程。已有研究表明,几种病毒会干扰 CREB 结合蛋白/小 e,西里尔文 300 的功能,调节它们的转录活性。在病毒感染期间,需要对宿主细胞基因表达模式进行重编程以建立适当的抗病毒反应,因此,许多病毒编码能够影响或干扰细胞信号以逃避炎症和免疫反应的蛋白质。包括小 e,西里尔文 300/CBP 在内的共激活因子蛋白的转录调控机制一直是深入研究的焦点。作为其中一部分,本文综述总结了病毒用来对抗宿主反应的一些分子手段及其在炎症和免疫反应调节中的作用。