Dual Roles of Host Zinc Finger Proteins in Viral RNA Regulation: Decay or Stabilization

Hyokyoung Lee1, Sung-Kyun Park2,3, Junghyun Lim1

  • 1Department of Pharmacy, School of Pharmacy and Institute of New Drug Development, Jeonbuk National University, Jeonju 54896, Republic of Korea.

Insights

Host RNA-binding proteins regulate viral RNA to combat infections. This review details zinc finger proteins, highlighting their dual roles and potential as antiviral therapy targets.

Area of Science:

  • Virology
  • Molecular Biology
  • Immunology

Background:

  • Host defense mechanisms against viral infections are critical for understanding viral diseases.
  • Host RNA-binding proteins (RBPs) are increasingly recognized for their roles in controlling viral replication.
  • RBPs can either restrict viral infections or promote viral persistence through interactions with cofactors.

Purpose of the Study:

  • To identify host proteins that regulate viral RNA, targeting viral components without harming host cells.
  • To review the dual roles of RNA-binding zinc finger proteins (ZNFPs) in viral RNA regulation.
  • To explore the therapeutic potential of ZNFPs in developing novel antiviral strategies.

Main Methods:

  • Literature review focusing on host RNA-binding proteins and their interaction with viral RNA.
  • Classification of RNA-binding zinc finger proteins into ZCCCH-type and ZCCHC-type.
  • Analysis of the functional diversity and mechanisms of ZNFPs in viral RNA regulation.

Main Results:

  • Several host RBPs, particularly zinc finger proteins, play pivotal roles in regulating viral RNA.
  • These ZNFPs exhibit dual functions: restricting viral replication or promoting viral persistence.
  • ZNFPs can either degrade viral genomes or stabilize them through interactions with cofactors.

Conclusions:

  • RNA-binding zinc finger proteins are key regulators of viral RNA, with diverse functional roles.
  • Understanding the dual functions of ZNFPs provides insights into viral infection dynamics.
  • ZNFPs represent promising therapeutic targets for the development of novel antiviral treatments.

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