Istituto di Virologia Vegetale del CNR, Unità Organizzativa di Bari, Bari, Italy.
J Gen Virol. 2010 Sep;91(Pt 9):2393-401. doi: 10.1099/vir.0.022046-0. Epub 2010 May 19.
The biological and molecular properties of a novel satellite RNA (satRNA L) associated with tomato bushy stunt virus (TBSV) are described. satRNA L consisted of a linear single-stranded RNA of 615 nt, lacked significant open reading frames (ORFs) and had no sequence identity with the helper genome other than in the 5'-proximal 7 nt and in a central region that is also conserved in all tombusvirus genomic, defective interfering and satellite RNAs. Secondary-structure analysis showed the presence of high-order domains similar to those described for other tombusvirus RNAs. Shorter-than-unit-length molecules were shown not to be related to a silencing mechanism. satRNA L did not modify the symptoms induced by TBSV under any of the temperature conditions tested. A full-length cDNA clone was constructed and used in co-inoculations with transcripts of carnation Italian ringspot virus (CIRV) and cymbidium ringspot virus (CymRSV). CIRV, but not CymRSV, supported the replication of satRNA L. Using CIRV-CymRSV hybrid infectious clones, two regions were identified as possible determinants of the different ability to support satRNA L replication. The first region was in the 5'-untranslated region, which folds differently in CymRSV in comparison with CIRV and TBSV; the second region was in the ORF1-encoded protein where a more efficient satRNA L-binding domain is suggested to be present in CIRV.
描述了与番茄丛矮病毒(TBSV)相关的新型卫星 RNA(satRNA L)的生物学和分子特性。satRNA L 由 615 个核苷酸组成的线性单链 RNA 组成,缺乏显著的开放阅读框(ORF),除了在 5'-近端 7 个核苷酸和中央区域与辅助基因组没有序列同一性外,该区域在所有 TBSV 基因组、缺陷干扰和卫星 RNA 中也是保守的。二级结构分析表明存在类似于其他 TBSV RNA 描述的高级结构域。证明短于单位长度的分子与沉默机制无关。在测试的任何温度条件下,satRNA L 都不会改变 TBSV 诱导的症状。构建了全长 cDNA 克隆,并与香石竹意大利环斑病毒(CIRV)和蝴蝶兰环斑病毒(CymRSV)的转录本进行共接种。CIRV 而不是 CymRSV 支持 satRNA L 的复制。使用 CIRV-CymRSV 杂交传染性克隆,鉴定出两个可能决定不同支持 satRNA L 复制能力的区域。第一个区域在 5'-非翻译区,与 CIRV 和 TBSV 相比,CymRSV 中的该区域折叠方式不同;第二个区域在 ORF1 编码蛋白中,建议在 CIRV 中存在更有效的 satRNA L 结合域。