Mechanisms and enzymes involved in SARS coronavirus genome expression
Author(s) -
Volker Thiel,
Konstantin A. Ivanov,
Ákos Putics,
Tobias Hertzig,
Barbara Schelle,
Sonja Bayer,
Benedikt Weißbrich,
Eric J. Snijder,
Holger F. Rabenau,
Hans Wilhelm Doerr,
Alexander E. Gorbalenya,
John Ziebuhr
Publication year - 2003
Publication title -
journal of general virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.55
H-Index - 167
eISSN - 1465-2099
pISSN - 0022-1317
DOI - 10.1099/vir.0.19424-0
Subject(s) - biology , coronavirus , subgenomic mrna , helicase , genome , virology , rna , rna helicase a , coronaviridae , viral replication , gene , genetics , computational biology , virus , covid-19 , medicine , disease , pathology , infectious disease (medical specialty)
A novel coronavirus is the causative agent of the current epidemic of severe acute respiratory syndrome (SARS). Coronaviruses are exceptionally large RNA viruses and employ complex regulatory mechanisms to express their genomes. Here, we determined the sequence of SARS coronavirus (SARS-CoV), isolate Frankfurt 1, and characterized key RNA elements and protein functions involved in viral genome expression. Important regulatory mechanisms, such as the (discontinuous) synthesis of eight subgenomic mRNAs, ribosomal frameshifting and post-translational proteolytic processing, were addressed. Activities of three SARS coronavirus enzymes, the helicase and two cysteine proteinases, which are known to be critically involved in replication, transcription and/or post-translational polyprotein processing, were characterized. The availability of recombinant forms of key replicative enzymes of SARS coronavirus should pave the way for high-throughput screening approaches to identify candidate inhibitors in compound libraries.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom