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10.1126/sciadv.abe7386

http://scihub22266oqcxt.onion/10.1126/sciadv.abe7386
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33547084!7864571!33547084
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suck abstract from ncbi


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pmid33547084      Sci+Adv 2021 ; 7 (6): ä
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  • Nsp1 protein of SARS-CoV-2 disrupts the mRNA export machinery to inhibit host gene expression #MMPMID33547084
  • Zhang K; Miorin L; Makio T; Dehghan I; Gao S; Xie Y; Zhong H; Esparza M; Kehrer T; Kumar A; Hobman TC; Ptak C; Gao B; Minna JD; Chen Z; Garcia-Sastre A; Ren Y; Wozniak RW; Fontoura BMA
  • Sci Adv 2021[Feb]; 7 (6): ä PMID33547084show ga
  • The ongoing unprecedented severe acute respiratory syndrome caused by the SARS-CoV-2 outbreak worldwide has highlighted the need for understanding viral-host interactions involved in mechanisms of virulence. Here, we show that the virulence factor Nsp1 protein of SARS-CoV-2 interacts with the host messenger RNA (mRNA) export receptor heterodimer NXF1-NXT1, which is responsible for nuclear export of cellular mRNAs. Nsp1 prevents proper binding of NXF1 to mRNA export adaptors and NXF1 docking at the nuclear pore complex. As a result, a significant number of cellular mRNAs are retained in the nucleus during infection. Increased levels of NXF1 rescues the Nsp1-mediated mRNA export block and inhibits SARS-CoV-2 infection. Thus, antagonizing the Nsp1 inhibitory function on mRNA export may represent a strategy to restoring proper antiviral host gene expression in infected cells.
  • |*Gene Expression[MESH]
  • |Active Transport, Cell Nucleus/genetics[MESH]
  • |Animals[MESH]
  • |COVID-19/*metabolism/virology[MESH]
  • |Chlorocebus aethiops[MESH]
  • |HEK293 Cells[MESH]
  • |Host Microbial Interactions/*genetics[MESH]
  • |Humans[MESH]
  • |Nuclear Pore/metabolism[MESH]
  • |Nucleocytoplasmic Transport Proteins/genetics/metabolism[MESH]
  • |RNA, Messenger/genetics/*metabolism[MESH]
  • |RNA-Binding Proteins/genetics/metabolism[MESH]
  • |SARS-CoV-2/chemistry/*metabolism[MESH]
  • |Transfection[MESH]
  • |Vero Cells[MESH]
  • |Viral Nonstructural Proteins/genetics/*metabolism[MESH]


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