scholarly journals A mechanical explanation of RNA pseudoknot function in programmed ribosomal frameshifting

Nature ◽  
2006 ◽  
Vol 441 (7090) ◽  
pp. 244-247 ◽  
Author(s):  
Olivier Namy ◽  
Stephen J. Moran ◽  
David I. Stuart ◽  
Robert J. C. Gilbert ◽  
Ian Brierley
2018 ◽  
Vol 46 (16) ◽  
pp. 8079-8089 ◽  
Author(s):  
Saki Matsumoto ◽  
Neva Caliskan ◽  
Marina V Rodnina ◽  
Asako Murata ◽  
Kazuhiko Nakatani

Cell ◽  
1989 ◽  
Vol 57 (4) ◽  
pp. 537-547 ◽  
Author(s):  
Ian Brierley ◽  
Paul Digard ◽  
Stephen C. Inglis

RNA ◽  
2020 ◽  
Vol 26 (4) ◽  
pp. 512-528
Author(s):  
Eliza Thulson ◽  
Erik W. Hartwick ◽  
Andrew Cooper-Sansone ◽  
Marcus A.C. Williams ◽  
Mary E. Soliman ◽  
...  

2011 ◽  
Vol 39 (20) ◽  
pp. 8952-8959 ◽  
Author(s):  
C.-H. Yu ◽  
M. H. Noteborn ◽  
C. W. A. Pleij ◽  
R. C. L. Olsthoorn

2020 ◽  
Vol 7 (1) ◽  
pp. 219-238
Author(s):  
Wesley D. Penn ◽  
Haley R. Harrington ◽  
Jonathan P. Schlebach ◽  
Suchetana Mukhopadhyay

Programmed ribosomal frameshifting (PRF) is a conserved translational recoding mechanism found in all branches of life and viruses. In bacteria, archaea, and eukaryotes PRF is used to downregulate protein production by inducing a premature termination of translation, which triggers messenger RNA (mRNA) decay. In viruses, PRF is used to drive the production of a new protein while downregulating the production of another protein, thus maintaining a stoichiometry optimal for productive infection. Traditionally, PRF motifs have been defined by the characteristics of two cis elements: a slippery heptanucleotide sequence followed by an RNA pseudoknot or stem-loop within the mRNA. Recently, additional cis and new trans elements have been identified that regulate PRF in both host and viral translation. These additional factors suggest PRF is an evolutionarily conserved process whose function and regulation we are just beginning to understand.


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