Related Experiment Video
Updated: Apr 23, 2026

MicroRNA-based Regulation of Picornavirus Tropism
Published on: February 6, 2017
Formation and working mechanism of the picornavirus VPg uridylylation complex
Yuna Sun1, Yu Guo2, Zhiyong Lou3
1National Laboratory of Macromolecules, Institute of Biophysics, Chinese Academy of Science, Beijing 100101, China; School of Medicine and MOE Key Laboratory of Protein Sciences, Tsinghua University, Beijing 100084, China.
Abstract:
The initiation of picornavirus replication is featured by the uridylylation of viral protein genome-linked (VPg). In this process, viral RNA-dependent RNA polymerase (RdRp) catalyzes two uridine monophosphate (UMP) molecules to the hydroxyl group of the third tyrosine residue of VPg. Subsequently, the uridylylated VPg (VPg-pUpU) functions as the protein primer to initiate the replication of the viral genome. Although a large body of functional and structural works has been performed to define individual snapshots for particular stages of the VPg uridylylation process, the formation, dynamics and mechanism of the whole VPg uridylylation complex still requires further elucidation. We would like to provide an overview of the current knowledge of the picornaviral VPg uridylylation complex in this paper.
Related Concept Videos
Coat Assembly and GTPases
Coat assembly depends on the local availability of phosphatidylinositol phosphates or PIPs and GTP-binding proteins. Adaptor proteins, which link the coat proteins to the membrane, bind to these PIPs and play a crucial role in controlling...
Protein Complex Assembly
Many viruses self-assemble into a fully functional unit using the infected host cell to...
Pinching-off of Coated Vesicles
Retrovirus Life Cycles
Leaky Scanning
Directing Proteins to the Rough Endoplasmic Reticulum

