Accessory proteins of SARS-CoV and other coronaviruses.
Identifieur interne : 000F71 ( PubMed/Curation ); précédent : 000F70; suivant : 000F72Accessory proteins of SARS-CoV and other coronaviruses.
Auteurs : Ding Xiang Liu [Singapour] ; To Sing Fung [Singapour] ; Kelvin Kian-Long Chong [Singapour] ; Aditi Shukla [Allemagne] ; Rolf Hilgenfeld [Allemagne]Source :
- Antiviral research [ 1872-9096 ] ; 2014.
Descripteurs français
- KwdFr :
- Animaux, Cadres ouverts de lecture, Coronavirus (), Coronavirus (génétique), Coronavirus (métabolisme), Humains, Infections à coronavirus (virologie), Protéines virales régulatrices ou accessoires (génétique), Protéines virales régulatrices ou accessoires (métabolisme), Virus du SRAS (génétique), Virus du SRAS (métabolisme).
- MESH :
- génétique : Coronavirus, Protéines virales régulatrices ou accessoires, Virus du SRAS.
- métabolisme : Coronavirus, Protéines virales régulatrices ou accessoires, Virus du SRAS.
- virologie : Infections à coronavirus.
- Animaux, Cadres ouverts de lecture, Coronavirus, Humains.
English descriptors
- KwdEn :
- Animals, Coronavirus (classification), Coronavirus (genetics), Coronavirus (metabolism), Coronavirus Infections (virology), Humans, Open Reading Frames, SARS Virus (genetics), SARS Virus (metabolism), Viral Regulatory and Accessory Proteins (genetics), Viral Regulatory and Accessory Proteins (metabolism).
- MESH :
- chemical , genetics : Viral Regulatory and Accessory Proteins.
- classification : Coronavirus.
- genetics : Coronavirus, SARS Virus.
- metabolism : Coronavirus, SARS Virus, Viral Regulatory and Accessory Proteins.
- virology : Coronavirus Infections.
- Animals, Humans, Open Reading Frames.
Abstract
The huge RNA genome of SARS coronavirus comprises a number of open reading frames that code for a total of eight accessory proteins. Although none of these are essential for virus replication, some appear to have a role in virus pathogenesis. Notably, some SARS-CoV accessory proteins have been shown to modulate the interferon signaling pathways and the production of pro-inflammatory cytokines. The structural information on these proteins is also limited, with only two (p7a and p9b) having their structures determined by X-ray crystallography. This review makes an attempt to summarize the published knowledge on SARS-CoV accessory proteins, with an emphasis on their involvement in virus-host interaction. The accessory proteins of other coronaviruses are also briefly discussed. This paper forms part of a series of invited articles in Antiviral Research on "From SARS to MERS: 10 years of research on highly pathogenic human coronaviruses" (see Introduction by Hilgenfeld and Peiris (2013)).
DOI: 10.1016/j.antiviral.2014.06.013
PubMed: 24995382
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pubmed:24995382Le document en format XML
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<front><div type="abstract" xml:lang="en">The huge RNA genome of SARS coronavirus comprises a number of open reading frames that code for a total of eight accessory proteins. Although none of these are essential for virus replication, some appear to have a role in virus pathogenesis. Notably, some SARS-CoV accessory proteins have been shown to modulate the interferon signaling pathways and the production of pro-inflammatory cytokines. The structural information on these proteins is also limited, with only two (p7a and p9b) having their structures determined by X-ray crystallography. This review makes an attempt to summarize the published knowledge on SARS-CoV accessory proteins, with an emphasis on their involvement in virus-host interaction. The accessory proteins of other coronaviruses are also briefly discussed. This paper forms part of a series of invited articles in Antiviral Research on "From SARS to MERS: 10 years of research on highly pathogenic human coronaviruses" (see Introduction by Hilgenfeld and Peiris (2013)).</div>
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<Abstract><AbstractText>The huge RNA genome of SARS coronavirus comprises a number of open reading frames that code for a total of eight accessory proteins. Although none of these are essential for virus replication, some appear to have a role in virus pathogenesis. Notably, some SARS-CoV accessory proteins have been shown to modulate the interferon signaling pathways and the production of pro-inflammatory cytokines. The structural information on these proteins is also limited, with only two (p7a and p9b) having their structures determined by X-ray crystallography. This review makes an attempt to summarize the published knowledge on SARS-CoV accessory proteins, with an emphasis on their involvement in virus-host interaction. The accessory proteins of other coronaviruses are also briefly discussed. This paper forms part of a series of invited articles in Antiviral Research on "From SARS to MERS: 10 years of research on highly pathogenic human coronaviruses" (see Introduction by Hilgenfeld and Peiris (2013)).</AbstractText>
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