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Enhancer-promoter activation by the Kaposi sarcoma-associated herpesvirus episome maintenance protein LANA

机译:卡波西肉瘤相关疱疹病毒游离体维持蛋白 LANA 激活增强子-启动子

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Higher -order genome structure influences the transcriptional regulation of cellular genes through the juxtaposition of regulatory elements, such as enhancers, close to promoters of target genes. While enhancer activation has emerged as an important facet of Kaposi sarcoma -associated herpesvirus (KSHV) biology, the mechanisms controlling enhancer -target gene expression remain obscure. Here, we discover that the KSHV genome tethering protein latency -associated nuclear antigen (LANA) potentiates enhancer -target gene expression in primary effusion lymphoma (PEL), a highly aggressive B cell lymphoma causally associated with KSHV. Genome-wide analyses demonstrate increased levels of enhancer RNA transcription as well as activating chromatin marks at LANA-bound enhancers. 3D genome conformation analyses identified genes critical for latency and tumorigenesis as targets of LANA-occupied enhancers, and LANA depletion results in their downregulation. These findings reveal a mechanism in enhancer -gene coordination and describe a role through which the main KSHV tethering protein regulates essential gene expression in PEL.
机译:高阶基因组结构通过靠近靶基因启动子的调控元件(如增强子)的并置影响细胞基因的转录调控。虽然增强子激活已成为卡波西肉瘤相关疱疹病毒 (KSHV) 生物学的一个重要方面,但控制增强子靶基因表达的机制仍然模糊不清。在这里,我们发现 KSHV 基因组拴系蛋白潜伏期相关核抗原 (LANA) 增强了原发性积液淋巴瘤 (PEL) 中的增强子靶基因表达,这是一种与 KSHV 因果相关的高度侵袭性 B 细胞淋巴瘤。全基因组分析表明增强子 RNA 转录水平升高,以及激活 LANA 结合增强子的染色质标记。3D 基因组构象分析确定了对潜伏期和肿瘤发生至关重要的基因作为 LANA 占据的增强子的靶标,LANA 耗竭导致其下调。这些发现揭示了增强子-基因协调的机制,并描述了主要的KSHV拴系蛋白调节PEL中必需基因表达的作用。

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