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从增强子到基因组构象:复杂的转录调控是单一疱疹病毒基因表达的基础。

From enhancers to genome conformation: complex transcriptional control underlies expression of a single herpesviral gene.

作者信息

Morgens David W, Gulyas Leah, Rivera-Madera Alejandro, Souza Annabelle S, Glaunsinger Britt A

机构信息

Department of Plant and Microbial Biology, UC Berkeley, Berkeley, CA, USA.

Department of Molecular and Cell Biology, UC Berkeley, CA, USA.

出版信息

bioRxiv. 2024 Jun 16:2023.07.08.548212. doi: 10.1101/2023.07.08.548212.

Abstract

Complex transcriptional control is a conserved feature of both eukaryotes and the viruses that infect them. Here, we illustrate this by combining high-density functional genomics, expression profiling, and viral-specific chromosome conformation capture to define with unprecedented detail the transcriptional regulation of a single gene, ORF68, from Kaposi's sarcoma-associated herpesvirus (KSHV). We first identified seven cis-regulatory regions by densely tiling the ~154 kb KSHV genome with CRISPRi. A parallel Cas9 nuclease screen indicated that three of these regions act as promoters of genes that regulate ORF68. RNA expression profiling demonstrated that three more of these regions act by either repressing or enhancing other distal viral genes involved in ORF68 transcriptional regulation. Finally, we tracked how the 3D structure of the viral genome changes during its lifecycle, revealing that these enhancing regulatory elements are physically closer to their targets when active, and that disrupting some elements caused large-scale changes to the 3D genome. These data enable us to construct a complete model revealing that the mechanistic diversity of this essential regulatory circuit matches that of human genes.

摘要

复杂的转录调控是真核生物以及感染它们的病毒的一个保守特征。在此,我们通过结合高密度功能基因组学、表达谱分析以及病毒特异性染色体构象捕获技术,以前所未有的详细程度定义了来自卡波西肉瘤相关疱疹病毒(KSHV)的单个基因ORF68的转录调控,以此来说明这一点。我们首先通过用CRISPRi密集覆盖约154 kb的KSHV基因组,鉴定出七个顺式调控区域。平行的Cas9核酸酶筛选表明,其中三个区域充当调控ORF68的基因的启动子。RNA表达谱分析表明,这些区域中的另外三个区域通过抑制或增强参与ORF68转录调控的其他远端病毒基因而起作用。最后,我们追踪了病毒基因组在其生命周期中的三维结构变化,发现这些增强调控元件在活跃时在物理上更接近其靶标,并且破坏某些元件会导致三维基因组发生大规模变化。这些数据使我们能够构建一个完整的模型,揭示这个基本调控回路的机制多样性与人类基因的机制多样性相匹配。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0373/11181378/31d7a506885d/nihpp-2023.07.08.548212v3-f0001.jpg

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