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10.7554/eLife.55799

http://scihub22266oqcxt.onion/10.7554/eLife.55799
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32427100!7282821!32427100
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suck abstract from ncbi


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pmid32427100      Elife 2020 ; 9 (ä): ä
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  • mRNA stem-loops can pause the ribosome by hindering A-site tRNA binding #MMPMID32427100
  • Bao C; Loerch S; Ling C; Korostelev AA; Grigorieff N; Ermolenko DN
  • Elife 2020[May]; 9 (ä): ä PMID32427100show ga
  • Although the elongating ribosome is an efficient helicase, certain mRNA stem-loop structures are known to impede ribosome movement along mRNA and stimulate programmed ribosome frameshifting via mechanisms that are not well understood. Using biochemical and single-molecule Forster resonance energy transfer (smFRET) experiments, we studied how frameshift-inducing stem-loops from E. coli dnaX mRNA and the gag-pol transcript of Human Immunodeficiency Virus (HIV) perturb translation elongation. We find that upon encountering the ribosome, the stem-loops strongly inhibit A-site tRNA binding and ribosome intersubunit rotation that accompanies translation elongation. Electron cryo-microscopy (cryo-EM) reveals that the HIV stem-loop docks into the A site of the ribosome. Our results suggest that mRNA stem-loops can transiently escape the ribosome helicase by binding to the A site. Thus, the stem-loops can modulate gene expression by sterically hindering tRNA binding and inhibiting translation elongation.
  • |*Nucleic Acid Conformation[MESH]
  • |*Ribosomes[MESH]
  • |Bacterial Proteins/genetics/metabolism[MESH]
  • |Cryoelectron Microscopy[MESH]
  • |DNA Polymerase III/genetics/metabolism[MESH]
  • |Escherichia coli/genetics/metabolism[MESH]
  • |Frameshifting, Ribosomal[MESH]
  • |Fusion Proteins, gag-pol[MESH]
  • |Gene Expression Regulation, Bacterial[MESH]
  • |Gene Expression Regulation, Viral[MESH]
  • |HIV-1/genetics/metabolism[MESH]
  • |RNA, Bacterial[MESH]
  • |RNA, Messenger/chemistry/*metabolism[MESH]


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