Structural and functional conservation of the programmed −1 ribosomal frameshift signal of SARS coronavirus 2 (SARS-CoV-2)

Author:

Kelly Jamie A.ORCID,Olson Alexandra N.,Neupane Krishna,Munshi Sneha,San Emeterio Josue,Pollack LoisORCID,Woodside Michael T.,Dinman Jonathan D.ORCID

Funder

HHS | NIH | National Institute of General Medical Sciences

Division of Intramural Research, National Institute of Allergy and Infectious Diseases

DOD | Defense Threat Reduction Agency

University of Maryland

Gouvernement du Canada | Canadian Institutes of Health Research

HHS | National Institutes of Health

U.S. Department of Energy

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference24 articles.

1. The species severe acute respiratory syndrome–related coronavirus: classifying 2019-nCoV and naming it SARS-CoV-2;Coronaviridae Study Group of the International Committee on Taxonomy of Viruses;Nat. Microbiol,2020

2. Coronavirus genome structure and replication;Brian,2005

3. Mechanisms and implications of programmed translational frameshifting;Dinman;Wiley Interdiscip. Rev. RNA,2012

4. Ribosomal frameshifting and transcriptional slippage: From genetic steganography and cryptography to adventitious use;Atkins;Nucleic Acids Res,2016

5. Expression of the Rous sarcoma virus pol gene by ribosomal frameshifting;Jacks;Science,1985

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