Torres Soleil, Jain Vaibhav, Stribling Daniel, Gay Lauren A, Naeem Muhammed, Baddoo Melody, Flemington Erik K, Tibbetts Scott A, Renne Rolf
Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, FL 32601, USA.
UF Genetics Institute, University of Florida, Gainesville, FL 32601, USA.
Explor Target Antitumor Ther. 2025 May 29;6:1002320. doi: 10.37349/etat.2025.1002320. eCollection 2025.
Circular RNA (circRNA) is a class of noncoding, single-stranded RNA generated by backsplicing, a process where the 5' and 3' ends of an RNA are covalently joined. Virally encoded circRNAs have been identified in several members of Gammaherpesvirinae, including Kaposi's sarcoma-associated herpesvirus (KSHV). In KSHV, the viral interferon regulatory factor 4 (vIRF4) region produces two isoforms of circRNA (circ-vIRF4) that are detectable during latency and reactivation. Given the growing literature implicating circRNA in human diseases, a role may exist for circ-vIRF4 in the development of KSHV malignancies. Therefore, the aim of this study is to characterize the function of vIRF4 circRNAs.
A KSHV mutant (Δcirc-vIRF4) was generated in the BAC16 bacmid and transfected into 293T and iSLK cells. Expression of circRNA after mutagenesis was assessed by qualitative and quantitative PCR. Host and viral gene expression in iSLK cells during both viral latency and reactivation were also assessed by RNA-seq.
RT-PCR of Δcirc-vIRF4-infected iSLK cells demonstrated no expression of wild-type (WT) isoforms, but PCR cloning showed that alternative backsplice sites were used to express novel vIRF4 circRNAs, where the most prominent isoform was a 1,020 nt isoform. RNA-seq analyses comparing WT- and Δcirc-vIRF4-infected iSLK cells demonstrated significant differential expression of both host and viral genes during both phases of the viral life cycle. Gene ontology analyses returned terms related to cell adhesion, proliferation, and migration for both datasets, as well as kinase signaling and apoptosis for the lytic dataset.
These results show that KSHV can switch to an alternative backsplice site for vIRF4 circRNA production in the absence of a canonical splice site and that circ-vIRF4 contributes to the regulation of both host and viral gene expression through an unknown mechanism.
环状RNA(circRNA)是一类通过反向剪接产生的非编码单链RNA,反向剪接是指RNA的5'端和3'端共价连接的过程。在γ疱疹病毒亚科的几个成员中已鉴定出病毒编码的circRNA,包括卡波西肉瘤相关疱疹病毒(KSHV)。在KSHV中,病毒干扰素调节因子4(vIRF4)区域产生两种circRNA异构体(circ-vIRF4),在潜伏和再激活期间均可检测到。鉴于越来越多的文献表明circRNA与人类疾病有关,circ-vIRF4可能在KSHV恶性肿瘤的发生发展中起作用。因此,本研究的目的是表征vIRF4 circRNA的功能。
在BAC16细菌人工染色体中构建KSHV突变体(Δcirc-vIRF4),并转染到293T和iSLK细胞中。通过定性和定量PCR评估诱变后circRNA的表达。还通过RNA测序评估iSLK细胞在病毒潜伏和再激活期间的宿主和病毒基因表达。
对感染Δcirc-vIRF4的iSLK细胞进行RT-PCR显示未表达野生型(WT)异构体,但PCR克隆表明使用了替代的反向剪接位点来表达新的vIRF4 circRNA,其中最突出的异构体是1020 nt的异构体。比较感染WT和Δcirc-vIRF4的iSLK细胞的RNA测序分析表明,在病毒生命周期的两个阶段,宿主和病毒基因均有显著差异表达。基因本体分析返回了两个数据集与细胞黏附、增殖和迁移相关的术语,以及裂解数据集与激酶信号传导和细胞凋亡相关的术语。
这些结果表明,在没有经典剪接位点的情况下,KSHV可以切换到替代的反向剪接位点来产生vIRF4 circRNA,并且circ-vIRF4通过未知机制参与宿主和病毒基因表达的调控。