Severe acute respiratory syndrome coronavirus nucleocapsid protein does not modulate transcription of the human FGL2 gene (Q39855254)

15 September 2017

Severe acute respiratory syndrome coronavirus nucleocapsid protein does not modulate transcription of the human FGL2 gene (English)

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severe acute respiratory syndrome

15 September 2017

nucleoprotein [SARS-Cov]

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based on heuristic

inferred from title

SARS-CoV-1

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1 reference

Kam-Leung Siu

1

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15 September 2017

Ching-Ping Chan

2

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15 September 2017

Chris Chan

3

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15 September 2017

Bo-Jian Zheng

4

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15 September 2017

Dong-Yan Jin

5

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15 September 2017

language of work or name

English

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publication date

7 May 2009

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Journal of General Virology

15 September 2017

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15 September 2017

90

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15 September 2017

Pt 9

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15 September 2017

2107-2113

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The nucleoprotein is required for efficient coronavirus genome replication.

15 September 2017

1 reference

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SARS-CoV nucleocapsid protein binds to hUbc9, a ubiquitin conjugating enzyme of the sumoylation system

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The nucleocapsid protein of SARS-CoV induces transcription of hfgl2 prothrombinase gene dependent on C/EBP alpha.

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Activation of AP-1 signal transduction pathway by SARS coronavirus nucleocapsid protein

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Human TRBP and PACT directly interact with each other and associate with dicer to facilitate the production of small interfering RNA

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Severe acute respiratory syndrome coronavirus open reading frame (ORF) 3b, ORF 6, and nucleocapsid proteins function as interferon antagonists

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Sumoylation of the nucleocapsid protein of severe acute respiratory syndrome coronavirus

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Gene transcription of fgl2 in endothelial cells is controlled by Ets‐1 and Oct‐1 and requires the presence of both Sp1 and Sp3

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SR-rich motif plays a pivotal role in recombinant SARS coronavirus nucleocapsid protein multimerization

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Characterization of N protein self-association in coronavirus ribonucleoprotein complexes

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Severe acute respiratory syndrome coronavirus nsp1 suppresses host gene expression, including that of type I interferon, in infected cells

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Lung pathology of fatal severe acute respiratory syndrome.

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The nucleocapsid protein of murine hepatitis virus type 3 induces transcription of the novel fgl2 prothrombinase gene

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Induction of prothrombinase fgl2 by the nucleocapsid protein of virulent mouse hepatitis virus is dependent on host hepatic nuclear factor-4 alpha

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Activation of TORC1 transcriptional coactivator through MEKK1-induced phosphorylation

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Severe acute respiratory syndrome coronavirus M protein inhibits type I interferon production by impeding the formation of TRAF3.TANK.TBK1/IKKepsilon complex.

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Adenosine promotes IL-6 release in airway epithelia.

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The severe acute respiratory syndrome coronavirus nucleocapsid protein is phosphorylated and localizes in the cytoplasm by 14-3-3-mediated translocation

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Nuclear/nucleolar localization properties of C-terminal nucleocapsid protein of SARS coronavirus

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Apical entry and release of severe acute respiratory syndrome-associated coronavirus in polarized Calu-3 lung epithelial cells

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Localization to the nucleolus is a common feature of coronavirus nucleoproteins, and the protein may disrupt host cell division

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Nucleocapsid protein of SARS-CoV activates the expression of cyclooxygenase-2 by binding directly to regulatory elements for nuclear factor-kappa B and CCAAT/enhancer binding protein.

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Severe acute respiratory syndrome (SARS) coronavirus-induced lung epithelial cytokines exacerbate SARS pathogenesis by modulating intrinsic functions of monocyte-derived macrophages and dendritic cells

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Subcellular localization of the severe acute respiratory syndrome coronavirus nucleocapsid protein.

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Trafficking motifs in the SARS-coronavirus nucleocapsid protein.

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The nucleocapsid protein of SARS-associated coronavirus inhibits B23 phosphorylation

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Nucleocapsid protein of SARS-CoV activates interleukin-6 expression through cellular transcription factor NF-kappaB.

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Severe acute respiratory syndrome-associated coronavirus nucleocapsid protein interacts with Smad3 and modulates transforming growth factor-beta signaling

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Coronavirus nucleocapsid protein is an RNA chaperone.

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Identifiers

DOI

10.1099/VIR.0.009209-0

1 reference

15 September 2017

1 reference