BmNPV interacts with super-enhancer regions of the host chromatin to hijack cellular transcription machinery.

IF 16.6 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shudi Zhao, Xingyang Wang, Tian Yang, Xinyu Zhu, Xiaofeng Wu
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引用次数: 0

Abstract

Effective transcriptional activation relies on the spatial interaction between specific DNA elements. DNA interactions have also been observed between DNA viruses and their hosts, with limited understanding of the involved details. Baculovirus is a representative species of DNA virus and has been reported to interact with the host genome in our previous study. However, the biological significance of the baculovirus-host trans-species DNA interaction and its underlying mechanisms remain elusive. Here, using Bombyx mori nucleopolyhedrovirus (BmNPV) as the model virus, we combine epigenome, transcriptome, and biochemical assays to investigate the baculovirus-host DNA interaction. Our data show that BmNPV hijacks the transcriptional regulatory capacity of host super-enhancers (SEs) by physically interacting with these regions on the host genome. This results in the usurpation of the activating capacity of an SE-binding transcription factor GATA by the virus, thereby impairing the SE-induced specific transcriptional activation of the target antiviral genes. Moreover, the hijacked regulatory capacity is spread on BmNPV genome through cis-interaction of viral DNA, leading to enhanced viral gene expression. Overall, our results provide novel insights into the intricate interplay of viruses with host gene expression regulatory networks and broaden the vision in the mechanisms of viral exploitation on cellular machinery.

BmNPV与宿主染色质的超增强子区域相互作用以劫持细胞转录机制。
有效的转录激活依赖于特定DNA元件之间的空间相互作用。DNA病毒与宿主之间的相互作用也被观察到,但对其中的细节了解有限。杆状病毒是一种具有代表性的DNA病毒,在我们之前的研究中已经报道过与宿主基因组相互作用。然而,杆状病毒-宿主跨物种DNA相互作用的生物学意义及其潜在机制仍然难以捉摸。本文以家蚕核多角体病毒(BmNPV)为模型病毒,结合表观基因组学、转录组学和生化分析,研究了杆状病毒与宿主DNA的相互作用。我们的数据表明,BmNPV通过与宿主基因组上的这些区域物理相互作用来劫持宿主超级增强子(se)的转录调控能力。这导致病毒篡夺se结合转录因子GATA的激活能力,从而损害se诱导的目标抗病毒基因的特异性转录激活。此外,劫持的调控能力通过病毒DNA的顺式相互作用在BmNPV基因组上传播,导致病毒基因表达增强。总的来说,我们的研究结果为病毒与宿主基因表达调控网络之间复杂的相互作用提供了新的见解,并拓宽了病毒利用细胞机制的视野。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
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