Abstract

Due to their exceptional simplicity of organization, viruses rely on the resources, molecular mechanisms, macromolecular complexes, regulatory pathways, and functional compartments of the host cell for an effective infection process. The nucleolus plays an important role in the process of interaction between the virus and the infected cell. The interactions of viral proteins and nucleic acids with the nucleolus during the infection process are universal phenomena and have been described for almost all taxonomic groups. During infection, proteins of the nucleolus in association with viral components can be directly used for the processes of replication and transcription of viral nucleic acids and the assembly and transport of viral particles. In the course of a viral infection, the usurpation of the nucleolus functions occurs and the usurpation is accompanied by profound changes in ribosome biogenesis. Recent studies have demonstrated that the nucleolus is a multifunctional and dynamic compartment. In addition to the biogenesis of ribosomes, it is involved in regulating the cell cycle and apoptosis, responding to cellular stress, repairing DNA, and transcribing RNA polymerase II-dependent genes. A viral infection can be accompanied by targeted transport of viral proteins to the nucleolus, massive release of resident proteins of the nucleolus into the nucleoplasm and cytoplasm, the movement of non-nucleolar proteins into the nucleolar compartment, and the temporary localization of viral nucleic acids in the nucleolus. The interaction of viral and nucleolar proteins interferes with canonical and non-canonical functions of the nucleolus and results in a change in the physiology of the host cell: cell cycle arrest, intensification or arrest of ribosome biogenesis, induction or inhibition of apoptosis, and the modification of signaling cascades involved in the stress response. The nucleolus is, therefore, an important target during viral infection. In this review, we discuss the functional impact of viral proteins and nucleic acid interaction with the nucleolus during infection.

Highlights

  • Introduction published maps and institutional affilThe nucleolus is the largest nuclear compartment

  • Nucleolar proteins can migrate from the nucleolus and, in association with viral proteins, participate in replicating and transcribing viral nucleic acids and assembly and the transport of viral particles in the nucleoplasm and cytoplasm

  • The virus and the host cell are in a state of constant combat, inventing an increasing number of mechanisms and counter-mechanisms to maintain an effective infection process and homeostasis of the host cell, respectively

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Summary

Nucleolus as the Source of Materials for Implementation of Infectious Process

We discussed the usage of the nucleolus as a specialized compartment in which the viral RNA matures and is prepared for transport to the cytoplasm and virions are assembled and stored. The association of nucleolin with the viral DNA polymerase component UL44 is required for efficient DNA replication and the expression of late proteins [49]. Typical nucleolar proteins move to the viral replicative centers, while both viral proteins and multiple cellular proteins move into the nucleolus, in particular, NUP210 (a component of the pore complex), PIK 3R6 (regulatory subunit of phosphoinositide kinase), and ribosomal protein S15a [35]. These observations are rather descriptive and the consequences of large-scale movements of cellular proteins during infection have not been characterized. Some viral caps are m7G caps; that is, primary snoRNAs are snatched in the nucleus prior to their cytosolic export [76]

Changes in Transcription of rDNA and Biogenesis of Ribosomes during
Modulation of the Cell Physiology during Viral Infection—Nucleolar Interface
Cell Cycle Modulation
Induction of Apoptosis
Protection against Apoptosis
Can Viruses Corrupt the Biocondensates Constituting the Nucleolus?
Conclusions
Nucleolus
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