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Phosphatidylinositol 4-kinases: hostages harnessed to build panviral replication platforms

Journal

TRENDS IN BIOCHEMICAL SCIENCES
Volume 37, Issue 7, Pages 293-302

Publisher

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tibs.2012.03.004

Keywords

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Funding

  1. National Institutes of Health [R01AI091985]
  2. National Science Foundation [MCB-0822058]
  3. Eunice Kennedy Shriver, National Institute of Child Health and Human Development of the National Institutes of Health

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Several RNA viruses have recently been shown to hijack members of the host phosphatidylinositol (PtdIns) 4-kinase (PI4K) family of enzymes. They use PI4K to generate membranes enriched in phosphatidylinositide 4-phosphate (PtdIns4P or PI4P) lipids, which can be used as replication platforms. Viral replication machinery is assembled on these platforms as a supramolecular complex and PtdIns4P lipids regulate viral RNA synthesis. This article highlights these recent studies on the regulation of viral RNA synthesis by PtdIns4P lipids. It explores the potential mechanisms by which PtdIns4P lipids can contribute to viral replication and discusses the therapeutic potential of developing antiviral molecules that target host PI4Ks as a form of panviral therapy.

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