Involvement of paraspeckle components in viral infections.

Nucleus (Austin, Tex.) Pub Date : 2024-12-01 Epub Date: 2024-05-08 DOI:10.1080/19491034.2024.2350178
Romane Milcamps, Thomas Michiels
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引用次数: 0

Abstract

Paraspeckles are non-membranous subnuclear bodies, formed through the interaction between the architectural long non-coding RNA (lncRNA) nuclear paraspeckle assembly transcript 1 (NEAT1) and specific RNA-binding proteins, including the three Drosophila Behavior/Human Splicing (DBHS) family members (PSPC1 (Paraspeckle Component 1), SFPQ (Splicing Factor Proline and Glutamine Rich) and NONO (Non-POU domain-containing octamer-binding protein)). Paraspeckle components were found to impact viral infections through various mechanisms, such as induction of antiviral gene expression, IRES-mediated translation, or viral mRNA polyadenylation. A complex involving NEAT1 RNA and paraspeckle proteins was also found to modulate interferon gene transcription after nuclear DNA sensing, through the activation of the cGAS-STING axis. This review aims to provide an overview on how these elements actively contribute to the dynamics of viral infections.

病毒感染中的副颈成分的参与。
副斑块是一种非膜状亚核体,由建筑长非编码 RNA(lncRNA)核副斑块组装转录本 1(NEAT1)与特定 RNA 结合蛋白相互作用形成、其中包括三个果蝇行为/人类剪接(DBHS)家族成员(PSPC1(Paraspeckle 组件 1)、SFPQ(剪接因子富脯氨酸和谷氨酰胺)和 NONO(含非 POU 结构域的八聚体结合蛋白))。研究发现,Paraspeckle 成分可通过多种机制影响病毒感染,如诱导抗病毒基因表达、IRES 介导的翻译或病毒 mRNA 多腺苷酸化。研究还发现,涉及 NEAT1 RNA 和副颈蛋白的复合物可通过激活 cGAS-STING 轴,在核 DNA 感测后调节干扰素基因转录。本综述旨在概述这些元素如何积极促进病毒感染的动态变化。
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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