Hughes P J, North C, Minor P D, Stanway G
Department of Biology, University of Essex, Wivenhoe Park, Colchester, U.K.
J Gen Virol. 1989 Nov;70 ( Pt 11):2943-52. doi: 10.1099/0022-1317-70-11-2943.
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.
我们已经确定了柯萨奇病毒A21(CAV - 21)的完整核苷酸序列,它是该肠道病毒亚组中首个得到详细分子分析的成员。该序列长度为7401个核苷酸,编码一个由2206个密码子组成的开放阅读框,其前面是一个711个核苷酸的5'非编码区,后面是一个72个核苷酸的3'非编码区以及一个多聚腺苷酸尾。最显著的特征是在基因组的3'部分与脊髓灰质炎病毒具有显著的同源性(氨基酸水平上大于90%)。基因组的其余部分同源性则低得多,这表明CAV - 21是一种重组病毒。类似于鼻病毒的特征,包括5'非编码区的长度以及密码子使用中轻微的-U/-A不平衡,可能与CAV - 21像鼻病毒一样感染上呼吸道这一事实有关。然而,该序列对于共享受体特异性的分子基础揭示甚少。