Literature DB >> 9735304

RNA binding and modulation of PKR activity.

S Gunnery1, M B Mathews.   

Abstract

PKR is an RNA-dependent protein kinase that is induced in mammalian cells by interferon treatment. It is present in a latent or inactive form in mammalian cells and is activated by very low concentrations of double-stranded (ds) RNA. Activated PKR phosphorylates eIF2, an essential initiation factor of protein synthesis, as well as other substrates including histone IIA, a 90-kDa protein from rabbit reticulocytes, the inhibitor, IkappaB, of the transcription factor, NF-kappaB, and the HIV-1 Tat protein. PKR interacts with several cellular and viral products and these interactions modulate its activation by dsRNA. Here we describe methods that are used to study the activation or inhibition of PKR by RNA modulators. Specifically, we detail (1) the purification of PKR from interferon-treated mammalian cells, (2) functional assays for PKR activation and inhibition in vitro, using purified enzyme or crude cell lysates, and (3) assays allowing evaluation of the binding of dsRNA and single-stranded RNA to PKR. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9735304     DOI: 10.1006/meth.1998.0623

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  9 in total

1.  The Hsp90 chaperone complex is both a facilitator and a repressor of the dsRNA-dependent kinase PKR.

Authors:  O Donzé; T Abbas-Terki; D Picard
Journal:  EMBO J       Date:  2001-07-16       Impact factor: 11.598

2.  Translational resistance of late alphavirus mRNA to eIF2alpha phosphorylation: a strategy to overcome the antiviral effect of protein kinase PKR.

Authors:  Iván Ventoso; Miguel Angel Sanz; Susana Molina; Juan José Berlanga; Luis Carrasco; Mariano Esteban
Journal:  Genes Dev       Date:  2006-01-01       Impact factor: 11.361

3.  Both carboxy- and amino-terminal domains of the vaccinia virus interferon resistance gene, E3L, are required for pathogenesis in a mouse model.

Authors:  T A Brandt; B L Jacobs
Journal:  J Virol       Date:  2001-01       Impact factor: 5.103

4.  Dual functions of Rift Valley fever virus NSs protein: inhibition of host mRNA transcription and post-transcriptional downregulation of protein kinase PKR.

Authors:  Tetsuro Ikegami; Krishna Narayanan; Sungyong Won; Wataru Kamitani; C J Peters; Shinji Makino
Journal:  Ann N Y Acad Sci       Date:  2009-09       Impact factor: 5.691

5.  Controlling activation of the RNA-dependent protein kinase by siRNAs using site-specific chemical modification.

Authors:  Sujiet Puthenveetil; Landon Whitby; Jin Ren; Kevin Kelnar; Joseph F Krebs; Peter A Beal
Journal:  Nucleic Acids Res       Date:  2006-09-18       Impact factor: 16.971

6.  PSMA-homing dsRNA chimeric protein vector kills prostate cancer cells and activates anti-tumor bystander responses.

Authors:  Yael Langut; Nufar Edinger; Efrat Flashner-Abramson; Naomi Melamed-Book; Mario Lebendiker; Yael Levi-Kalisman; Shoshana Klein; Alexander Levitzki
Journal:  Oncotarget       Date:  2017-04-11

7.  Rift Valley fever virus NSs protein promotes post-transcriptional downregulation of protein kinase PKR and inhibits eIF2alpha phosphorylation.

Authors:  Tetsuro Ikegami; Krishna Narayanan; Sungyong Won; Wataru Kamitani; C J Peters; Shinji Makino
Journal:  PLoS Pathog       Date:  2009-02-06       Impact factor: 6.823

Review 8.  Alphavirus Infection: Host Cell Shut-Off and Inhibition of Antiviral Responses.

Authors:  Jelke J Fros; Gorben P Pijlman
Journal:  Viruses       Date:  2016-06-11       Impact factor: 5.048

Review 9.  Cellular autophagy: surrender, avoidance and subversion by microorganisms.

Authors:  Karla Kirkegaard; Matthew P Taylor; William T Jackson
Journal:  Nat Rev Microbiol       Date:  2004-04       Impact factor: 60.633

  9 in total

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