Nucleotide sequence of the human coronavirus 229E RNA polymerase locus
- PMID: 8337838
- PMCID: PMC7131648
- DOI: 10.1006/viro.1993.1419
Nucleotide sequence of the human coronavirus 229E RNA polymerase locus
Abstract
The nucleotide sequence of the human coronavirus 229E (HCV 229E) RNA polymerase gene and the 5' region of the genome has been determined. The polymerase gene is comprised of two large open reading frames, ORF1a and ORF1b, that contain 4086 and 2687 codons, respectively. ORF1b overlaps ORF1a by 43 bases in the (-1) reading frame. The in vitro translation of SP6 transcripts which include HCV 229E sequences encompassing the ORF1a/ORF1b junction show that expression of ORF1b can be mediated by ribosomal frame-shifting. The predicted translation products of ORF1a (454,200 molecular weight) and ORF1a/1b (754,200 molecular weight) have been compared to the predicted RNA polymerase gene products of infectious bronchitis virus (IBV) and murine hepatitis virus (MHV) and conserved structural features and putative functional domains have been identified. This analysis completes the nucleotide sequence of the HCV 229E genome.
Similar articles
-
Complete sequence (20 kilobases) of the polyprotein-encoding gene 1 of transmissible gastroenteritis virus.Virology. 1995 Feb 1;206(2):817-22. doi: 10.1006/viro.1995.1004. Virology. 1995. PMID: 7856095 Free PMC article.
-
Equine arteritis virus is not a togavirus but belongs to the coronaviruslike superfamily.J Virol. 1991 Jun;65(6):2910-20. doi: 10.1128/JVI.65.6.2910-2920.1991. J Virol. 1991. PMID: 1851863 Free PMC article.
-
The primary structure and expression of the second open reading frame of the polymerase gene of the coronavirus MHV-A59; a highly conserved polymerase is expressed by an efficient ribosomal frameshifting mechanism.Nucleic Acids Res. 1990 Apr 11;18(7):1825-32. doi: 10.1093/nar/18.7.1825. Nucleic Acids Res. 1990. PMID: 2159623 Free PMC article.
-
Functional and genetic analysis of coronavirus replicase-transcriptase proteins.PLoS Pathog. 2005 Dec;1(4):e39. doi: 10.1371/journal.ppat.0010039. Epub 2005 Dec 9. PLoS Pathog. 2005. PMID: 16341254 Free PMC article. Review.
-
The complete nucleotide sequence of avian infectious bronchitis virus: analysis of the polymerase-coding region.Adv Exp Med Biol. 1987;218:15-29. doi: 10.1007/978-1-4684-1280-2_3. Adv Exp Med Biol. 1987. PMID: 2829522 Review. No abstract available.
Cited by
-
Inhibition of SARS-CoV-2 3CL Mpro by Natural and Synthetic Inhibitors: Potential Implication for Vaccine Production Against COVID-19.Front Mol Biosci. 2021 Apr 12;8:640819. doi: 10.3389/fmolb.2021.640819. eCollection 2021. Front Mol Biosci. 2021. PMID: 33912587 Free PMC article.
-
Homology Models and Molecular Dynamics Simulations of Main Proteinase from Coronavirus Associated with Severe Acute Respiratory Syndrome (SARS).J Chin Chem Soc. 2004 Oct;51(5A):889-900. doi: 10.1002/jccs.200400134. Epub 2013 Sep 25. J Chin Chem Soc. 2004. PMID: 32336761 Free PMC article.
-
The Genome Organization of the Nidovirales: Similarities and Differences between Arteri-, Toro-, and Coronaviruses.Semin Virol. 1997 Feb;8(1):33-47. doi: 10.1006/smvy.1997.0104. Epub 2002 May 25. Semin Virol. 1997. PMID: 32288441 Free PMC article.
-
A human RNA viral cysteine proteinase that depends upon a unique Zn2+-binding finger connecting the two domains of a papain-like fold.J Biol Chem. 1999 May 21;274(21):14918-25. doi: 10.1074/jbc.274.21.14918. J Biol Chem. 1999. PMID: 10329692 Free PMC article.
-
Severe acute respiratory syndrome coronavirus 3C-like proteinase N terminus is indispensable for proteolytic activity but not for enzyme dimerization. Biochemical and thermodynamic investigation in conjunction with molecular dynamics simulations.J Biol Chem. 2005 Jan 7;280(1):164-73. doi: 10.1074/jbc.M408211200. Epub 2004 Oct 26. J Biol Chem. 2005. PMID: 15507456 Free PMC article.
Publication types
MeSH terms
Substances
Associated data
- Actions
LinkOut - more resources
Full Text Sources
Other Literature Sources
