Sznarkowska Alicja, Mikac Sara, Pilch Magdalena
International Center for Cancer Vaccine Science, University of Gdansk, 80-308 Gdansk, Poland.
Cancers (Basel). 2020 May 4;12(5):1155. doi: 10.3390/cancers12051155.
Viral-derived elements and non-coding RNAs that build up "junk DNA" allow for flexible and context-dependent gene expression. They are extremely dense in the MHC region, accounting for flexible expression of the MHC I, II, and III genes and adjusting the level of immune response to the environmental stimuli. This review brings forward the viral-mediated aspects of the origin and evolution of adaptive immunity and aims to link this perspective with the MHC class I regulation. The complex regulatory network behind MHC expression is largely controlled by virus-derived elements, both as binding sites for immune transcription factors and as sources of regulatory non-coding RNAs. These regulatory RNAs are imbalanced in cancer and associate with different tumor types, making them promising targets for diagnostic and therapeutic interventions.
构成“垃圾DNA”的病毒衍生元件和非编码RNA可实现灵活且依赖于上下文的基因表达。它们在MHC区域极为密集,这使得MHC I、II和III类基因能够灵活表达,并调节对环境刺激的免疫反应水平。本综述提出了适应性免疫起源和进化的病毒介导方面,并旨在将这一观点与MHC I类调节联系起来。MHC表达背后的复杂调控网络在很大程度上由病毒衍生元件控制,这些元件既是免疫转录因子的结合位点,也是调控性非编码RNA的来源。这些调控RNA在癌症中失衡,并与不同的肿瘤类型相关,使其成为诊断和治疗干预的有前景的靶点。