Journal of General Virology · 1989 · 102 citations · 34 references
Life SciencesMolecular BiologyMolecular GeneticsGenomicsMolecular VirologyVirologyAnimal VirusesViral GeneticsViral Genome OrganizationViral GenomicsViral InfectionsVirus Genome OrganizationCodon Usage BiasCodon Usage EvolutionHomologyOpen Reading Frame LengthReceptor Binding SpecificityRespiratory VirusesRhinovirus Infection
We have determined the complete nucleotide sequence of coxsackievirus A21 (CAV-21), the first member of this enterovirus subgroup to be analysed in molecular detail. The sequence, which is 7401 nucleotides long, encodes an open reading frame of 2206 codons, preceded by a 5' non-coding region of 711 nucleotides and followed by a 3' non-coding region of 72 nucleotides plus a poly(A) tract. The most striking feature is the remarkable homology to the poliovirus (greater than 90% at the amino acid level) in the 3' part of the genome. The rest of the genome is much less homologous, suggesting that CAV-21 is a recombinant virus. Rhinovirus-like characteristics, including the length of the 5' non-coding region and a slight --U/--A imbalance in codon usage, may be related to the fact that CAV-21, like rhinoviruses, infects the upper respiratory tract. However, the sequence sheds little light on the molecular basis of the shared receptor specificity.
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Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase
Randall K. Saiki, David H. Gelfand, Susanne Stoffel et al. · Science · 1988 · 17.2K citations
The major human rhinovirus receptor is ICAM-1
Jeffrey M. Greve, Gary L. Davis, Ann Meyer et al. · Cell · 1989 · 1.1K citations