Literature DB >> 26937026

Hepatitis C Virus Exploitation of Processing Bodies.

Jason M Biegel1, Cara T Pager2.   

Abstract

During infection, positive-strand RNA viruses subvert cellular machinery involved in RNA metabolism to translate viral proteins and replicate viral genomes to avoid or disable the host defense mechanisms. Cytoplasmic RNA granules modulate the stabilities of cellular and viral RNAs. Understanding how hepatitis C virus and other flaviviruses interact with the host machinery required for protein synthesis, localization, and degradation of mRNAs is important for elucidating how these processes occur in both virus-infected and uninfected cells.
Copyright © 2016, American Society for Microbiology. All Rights Reserved.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 26937026      PMCID: PMC4859705          DOI: 10.1128/JVI.03056-15

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  18 in total

Review 1.  Interaction of host cell microRNAs with the HCV RNA genome during infection of liver cells.

Authors:  Cecilia D Sedano; Peter Sarnow
Journal:  Semin Liver Dis       Date:  2015-01-29       Impact factor: 6.115

2.  Stabilization of hepatitis C virus RNA by an Ago2-miR-122 complex.

Authors:  Tetsuro Shimakami; Daisuke Yamane; Rohit K Jangra; Brian J Kempf; Carolyn Spaniel; David J Barton; Stanley M Lemon
Journal:  Proc Natl Acad Sci U S A       Date:  2012-01-03       Impact factor: 11.205

3.  Dual regulation of hepatitis C viral RNA by cellular RNAi requires partitioning of Ago2 to lipid droplets and P-bodies.

Authors:  Svitlana Yu Berezhna; Lubica Supekova; Mary J Sever; Peter G Schultz; Ashok A Deniz
Journal:  RNA       Date:  2011-08-25       Impact factor: 4.942

4.  Modulation of hepatitis C virus RNA abundance and virus release by dispersion of processing bodies and enrichment of stress granules.

Authors:  Cara T Pager; Sylvia Schütz; Teresa M Abraham; Guangxiang Luo; Peter Sarnow
Journal:  Virology       Date:  2012-11-09       Impact factor: 3.616

5.  Hepatitis C virus infection inhibits P-body granule formation in human livers.

Authors:  Gemma Pérez-Vilaró; Carlos Fernández-Carrillo; Laura Mensa; Rosa Miquel; Xavier Sanjuan; Xavier Forns; Sofía Pérez-del-Pulgar; Juana Díez
Journal:  J Hepatol       Date:  2014-11-21       Impact factor: 25.083

Review 6.  The DHH1/RCKp54 family of helicases: an ancient family of proteins that promote translational silencing.

Authors:  Vlad Presnyak; Jeff Coller
Journal:  Biochim Biophys Acta       Date:  2013-03-23

Review 7.  Diversion of stress granules and P-bodies during viral infection.

Authors:  Lucas C Reineke; Richard E Lloyd
Journal:  Virology       Date:  2013-01-03       Impact factor: 3.616

8.  XRN1 stalling in the 5' UTR of Hepatitis C virus and Bovine Viral Diarrhea virus is associated with dysregulated host mRNA stability.

Authors:  Stephanie L Moon; Jeffrey G Blackinton; John R Anderson; Mary K Dozier; Benjamin J T Dodd; Jack D Keene; Carol J Wilusz; Shelton S Bradrick; Jeffrey Wilusz
Journal:  PLoS Pathog       Date:  2015-03-06       Impact factor: 6.823

9.  Hepatitis C virus genetics affects miR-122 requirements and response to miR-122 inhibitors.

Authors:  Benjamin Israelow; Gavriel Mullokandov; Judith Agudo; Marion Sourisseau; Ali Bashir; Andres Y Maldonado; Arvin C Dar; Brian D Brown; Matthew J Evans
Journal:  Nat Commun       Date:  2014-11-18       Impact factor: 14.919

10.  The structural basis of pathogenic subgenomic flavivirus RNA (sfRNA) production.

Authors:  Erich G Chapman; David A Costantino; Jennifer L Rabe; Stephanie L Moon; Jeffrey Wilusz; Jay C Nix; Jeffrey S Kieft
Journal:  Science       Date:  2014-04-18       Impact factor: 47.728

View more
  2 in total

1.  KSHV RNA-binding protein ORF57 inhibits P-body formation to promote viral multiplication by interaction with Ago2 and GW182.

Authors:  Nishi R Sharma; Vladimir Majerciak; Michael J Kruhlak; Lulu Yu; Jeong Gu Kang; Acong Yang; Shuo Gu; Marvin J Fritzler; Zhi-Ming Zheng
Journal:  Nucleic Acids Res       Date:  2019-09-26       Impact factor: 16.971

2.  Transcriptional responses of LSm14A after infection of blue eggshell layers with Newcastle disease viruses.

Authors:  Lang Tian; Changhua Wu; Guilan Wen; Changhong Li
Journal:  J Vet Med Sci       Date:  2019-09-18       Impact factor: 1.267

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.