About: Regulation of stress granules in virus systems

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An Entity of Type : schema:ScholarlyArticle, within Data Space : covidontheweb.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	Regulation of stress granules in virus systems
Creator	Lloyd, Richard White, James
Source	Elsevier; Medline; PMC
abstract	Virus infection initiates a number of cellular stress responses that modulate gene regulation and compartmentalization of RNA. Viruses must control host gene expression and the localization of viral RNAs to be successful parasites. RNA granules such as stress granules and processing bodies (PBs) contain translationally silenced messenger ribonucleoproteins (mRNPs) and serve as extensions of translation regulation in cells, storing transiently repressed mRNAs. New reports show a growing number of virus families modulate RNA granule function to maximize replication efficiency. This review summarizes recent advances in understanding the relationship between viruses and mRNA stress granules in animal cells and will discuss important questions that remain in this emerging field.
has issue date	2012-04-01(xsd:dateTime)
bibo:doi	10.1016/j.tim.2012.02.001
bibo:pmid	22405519
has license	green-oa
sha1sum (hex)	08a3e8af143f9b97a9ba5220f0de0fe0ae1bba06
schema:url	https://doi.org/10.1016/j.tim.2012.02.001
resource representing a document's title	Regulation of stress granules in virus systems
has PubMed Central identifier	PMC3322245
has PubMed identifier	22405519
schema:publication	Trends in Microbiology
resource representing a document's body	covid:08a3e8af143f9b97a9ba5220f0de0fe0ae1bba06#body_text
is schema:about of	named entity 'expression' named entity 'stress granules' named entity 'silenced' named entity 'regulation' named entity 'RNA' named entity 'viruses' named entity 'parasites' named entity 'families' named entity 'stress granules' named entity 'infection' named entity 'cellular stress' named entity 'RNA' named entity 'mRNAs' named entity 'viruses' named entity 'virus' named entity 'animal cells' named entity 'eIF4A' named entity 'infection' named entity 'DDX6' named entity 'eIF4GI' named entity 'eIF2α' named entity 'TIA-1' named entity 'T-cell' named entity 'pro-apoptotic' named entity 'viruses' named entity 'TIA-1' named entity 'HCV' named entity 'exogenous' named entity 'phenotypes' named entity 'virus infection' named entity 'Phosphorylate' named entity 'arginine' named entity 'DDX6' named entity 'PBs' named entity 'nutrient' named entity 'phosphorylation' named entity 'Poliovirus' named entity 'HCV' named entity 'initiation factors' named entity 'phosphorylation' named entity 'infection' named entity 'Herpes simplex' named entity 'Grb7' named entity 'exogenous' named entity 'TIA-1' named entity 'G3BP' named entity 'cytoplasmic' named entity 'interact' named entity 'eIF2' named entity 'flavivirus' named entity 'protein' named entity 'phosphorylation' named entity 'infection' named entity 'phosphorylation' named entity 'post-translationally modified' named entity 'Hepatitis C virus' named entity 'dsRNA' named entity 'cell-type' named entity 'West Nile' named entity 'eIF2α' named entity 'mRNA' named entity 'HIV-1' named entity 'viruses' named entity 'virus' named entity 'TIA-1' named entity 'RFs' named entity 'flaviviruses' named entity 'vRNA' named entity 'core protein' named entity 'P-bodies' named entity 'HCV' named entity 'Vaccinia virus' named entity 'cellular processes' named entity 'hpi' named entity 'metabolism' named entity 'infection' named entity 'host cell protein' named entity 'glutamine' named entity 'G3BP' named entity 'JNK'

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