Duke G M, Palmenberg A C
Department of Biochemistry, University of Wisconsin, Madison 53706.
J Virol. 1989 Apr;63(4):1822-6. doi: 10.1128/JVI.63.4.1822-1826.1989.
Mengovirus RNA transcripts with 5' noncoding poly(C) tracts of C8, C12, and C13UC10 have been synthesized in vitro from cDNA clones and shown to be infectious to HeLa cells. A chimeric clone has also been constructed which links the 5' end from one mengovirus clone (299 nucleotides, containing C13UC10) to a 7,424-base fragment derived from the 3' end of encephalomyocarditis (EMC) virus. Progeny virus isolated after transfection with the clone-derived RNAs had the same poly(C) tracts, mengovirus-specific sequences, or EMC virus-specific sequences as the transcript from which it was derived. Although the cloned poly(C) tracts were considerably shorter than those found in viral RNA from mengovirus (C50UC10) or EMC virus (C115UCUC3UC10), the growth characteristics of the progeny viruses in HeLa cells were indistinguishable from those of the parental viruses, indicating the length of this tract does not play a significant restrictive role for cardiovirus infectivity in tissue culture.
已从cDNA克隆体外合成了具有C8、C12和C13UC10的5'非编码聚(C)序列的脑心肌炎病毒RNA转录本,并证明其对HeLa细胞具有感染性。还构建了一个嵌合克隆,它将一个脑心肌炎病毒克隆的5'端(299个核苷酸,包含C13UC10)与源自脑心肌炎(EMC)病毒3'端的7424个碱基的片段连接起来。用克隆衍生的RNA转染后分离出的子代病毒具有与衍生它的转录本相同的聚(C)序列、脑心肌炎病毒特异性序列或EMC病毒特异性序列。尽管克隆的聚(C)序列比在脑心肌炎病毒(C50UC10)或EMC病毒(C115UCUC3UC10)的病毒RNA中发现的序列短得多,但子代病毒在HeLa细胞中的生长特性与亲代病毒无法区分,这表明该序列的长度对组织培养中的心病毒感染性没有显著的限制作用。