Lee Y S, Hsu Y H, Lin N S
Institute of Botany, Academia Sinica, Taipei, Taiwan.
J Virol. 2000 Nov;74(22):10341-8. doi: 10.1128/jvi.74.22.10341-10348.2000.
Satellite RNA of bamboo mosaic potexvirus (satBaMV), a single-stranded positive-sense RNA encoding a nonstructural protein of 20 kDa (P20), depends on bamboo mosaic potexvirus (BaMV) for replication and encapsidation. A full-length cDNA clone of satBaMV was used to examine the sequences required for the synthesis of potexvirus subgenomic RNAs (sgRNAs). Subgenomic promoter-like sequences (SGPs), 107 nucleotides (nt) upstream from the capsid protein (CP) gene of BaMV-V, were inserted upstream of the start codon of the P20 gene of satBaMV. Insertion of SGPs gave rise to the synthesis of sgRNA of satBaMV in protoplasts of Nicotiana benthamiana and leaves of Chenopodium quinoa when coinoculated with BaMV-V genomic RNA. Moreover, both the satBaMV cassette and its sgRNA were encapsidated. From analysis of the SGPs by deletion mutation, we concluded that an SGP contains one core promoterlike sequence (nt -30 through +16), two upstream enhancers (nt -59 through -31 and -91 through -60), and one downstream enhancer (nt +17 through +52), when the transcription initiation site is taken as +1. Site-directed mutagenesis and compensatory mutation to disrupt and restore potential base pairing in the core promoter-like sequence suggest that the stem-loop structure is important for the function of SGP in vivo. Likewise, the insertion of a putative SGP of the BaMV open reading frame 2 gene or a heterologous SGP of potato virus X resulted in generation of an sgRNA. The satBaMV cassette should be a useful tool to gain insight into sequences required for the synthesis of potexvirus sgRNAs.
竹花叶病毒卫星RNA(satBaMV)是一种单链正义RNA,编码一种20 kDa的非结构蛋白(P20),其复制和衣壳化依赖于竹花叶病毒(BaMV)。利用satBaMV的全长cDNA克隆来检测合成马铃薯X病毒亚基因组RNA(sgRNAs)所需的序列。将位于BaMV-V衣壳蛋白(CP)基因上游107个核苷酸(nt)的亚基因组启动子样序列(SGPs)插入到satBaMV的P20基因起始密码子上游。当与BaMV-V基因组RNA共接种时,SGPs的插入导致在本氏烟草原生质体和藜麦叶片中合成satBaMV的sgRNA。此外,satBaMV盒及其sgRNA均被衣壳化。通过缺失突变对SGPs进行分析,我们得出结论,当转录起始位点设为+1时,一个SGP包含一个核心启动子样序列(nt -30至+16)、两个上游增强子(nt -59至-31和-91至-60)和一个下游增强子(nt +17至+52)。对核心启动子样序列中潜在碱基配对进行破坏和恢复的定点诱变和补偿性突变表明,茎环结构对SGP在体内的功能很重要。同样,插入BaMV开放阅读框2基因的一个推定SGP或马铃薯X病毒的一个异源SGP导致产生一个sgRNA。satBaMV盒应该是深入了解马铃薯X病毒sgRNAs合成所需序列的一个有用工具。