Viral RNA Interactome: The Ultimate Researcher's Guide to RNA-Protein Interactions

被引:0
|
作者
Hanson, Wesley A. [1 ]
Agosto, Gabriel A. Romero [1 ]
Rouskin, Silvi [1 ]
机构
[1] Harvard Med Sch, Blavatnik Inst, Dept Microbiol, Boston, MA 02115 USA
来源
VIRUSES-BASEL | 2024年 / 16卷 / 11期
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
RNA-binding protein (RBP); RNA-protein interactome; RNA secondary structure; virus-host interactome; RNA chemical probing; HEPATITIS-C VIRUS; RIBOSOME ENTRY SITE; TRANSLATION INITIATION; WIDE IDENTIFICATION; SECONDARY STRUCTURE; ANTIVIRAL ACTIVITY; BINDING PROTEIN; TARGET; GENOME; DISCOVERY;
D O I
10.3390/v16111702
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
RNA molecules in the cell are bound by a multitude of RNA-binding proteins (RBPs) with a variety of regulatory consequences. Often, interactions with these RNA-binding proteins are facilitated by the complex secondary and tertiary structures of RNA molecules. Viral RNAs especially are known to be heavily structured and interact with many RBPs, with roles including genome packaging, immune evasion, enhancing replication and transcription, and increasing translation efficiency. As such, the RNA-protein interactome represents a critical facet of the viral replication cycle. Characterization of these interactions is necessary for the development of novel therapeutics targeted at the disruption of essential replication cycle events. In this review, we aim to summarize the various roles of RNA structures in shaping the RNA-protein interactome, the regulatory roles of these interactions, as well as up-to-date methods developed for the characterization of the interactome and directions for novel, RNA-directed therapeutics.
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页数:22
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