Department of Plant Pathology, University of Florida, Citrus Research and Education Center, Lake Alfred, FL 33850, USA.
Mol Plant Pathol. 2005 Mar 1;6(2):165-76. doi: 10.1111/j.1364-3703.2005.00275.x.
SUMMARY Citrus tristeza virus (CTV) has within the 3'-half of the genome ten open reading frames (ORFs) that are expressed through a series of 3'-coterminal subgenomic (sg) messenger (m)RNAs that, in general, function as monocistronic mRNAs with only the 5'-most ORF translated. Yet only nine sg mRNAs have been detected, suggesting that ORF 3, which is predicted to encode a small hydrophobic protein of approximately 6 kDa (p6), might be expressed in some other manner, perhaps from a functionally dicistronic sg mRNA. However, when we positioned the p6 gene near the 3'-terminus of a minimal CTV replicon to amplify greatly the level of production of the putative sg mRNA, we found a minimal level of a p6 mRNA, thus providing evidence for a separate mRNA for each 3' ORF. The 5' termini of the sg mRNAs and the cis-acting elements (controller elements-CEs) that regulate the production of the p6 gene and the adjacent HSP70h (heat shock protein 70 homologue) were located further upstream of the ORFs compared with the other CTV CEs. Both preferentially initiated synthesis with an adenylate, as has been shown for the more highly expressed 3' genes; but in contrast, the p6 sg mRNA occasionally initiated with a guanylate. Although the nucleotide sequences and the computer-predicted secondary structures of the HSP70h CE were similar to those previously described for other 3' CEs, those of the p6 CE were quite different, suggesting that CE strength is related to proximity to an ideal CE conformation. The lack of similarity between different CTV CEs led us to examine how well the CTV replicase complex could initiate sg mRNAs from CEs from different members of the family Closteroviridae. We found that the CTV replicase complex efficiently initiated production of sgRNAs from the p6 and HSP70h CEs from Beet yellows virus, with the HSP70h CE initiating at the same nucleotide as within the homologous virus, indicating that the mode of recognition of the CEs is similar. However, CEs from a more distantly related member of the Closteroviridae, Lettuce infectious yellows virus, did not function to produce sg mRNAs in CTV.
柑橘衰退病毒(CTV)在基因组的 3' 端有十个开放阅读框(ORF),通过一系列 3' 端共终止亚基因组(sg)信使(mRNA)表达,这些 mRNA 通常作为单顺反子 mRNA 发挥作用,只有 5' 端的 ORF 被翻译。然而,只检测到了九个 sg mRNA,这表明预测编码约 6 kDa(p6)小疏水蛋白的 ORF3 可能以某种其他方式表达,也许是从功能上的双顺反子 sg mRNA 表达。然而,当我们将 p6 基因定位在最小 CTV 复制子的 3' 末端,以大大扩增假定的 sg mRNA 的产生水平时,我们发现了 p6 mRNA 的最小水平,从而为每个 3'ORF 提供了单独的 mRNA 的证据。sg mRNA 的 5' 末端和调节 p6 基因和相邻 HSP70h(热休克蛋白 70 同源物)产生的顺式作用元件(控制器元件-CEs)比其他 CTV CEs 更上游定位。与其他 CTV CEs 相比,这两种元件都优先以腺苷酸起始合成,就像高度表达的 3' 基因一样;但相反,p6sgmRNA 偶尔以鸟苷酸起始。尽管 HSP70hCE 的核苷酸序列和计算机预测的二级结构与之前描述的其他 3'CEs 相似,但 p6CE 的序列却大不相同,这表明 CE 强度与接近理想的 CE 构象有关。不同 CTV CEs 之间缺乏相似性,促使我们研究 CTV 复制酶复合物如何从家族 Closteroviridae 不同成员的 CEs 起始 sgmRNA。我们发现 CTV 复制酶复合物能够有效地从 Beet yellows virus 的 p6 和 HSP70hCE 起始 sgRNA 的产生,HSP70hCE 在与同源病毒相同的核苷酸处起始,表明 CEs 的识别模式相似。然而,来自 Closteroviridae 中亲缘关系较远的成员 Lettuce infectious yellows virus 的 CEs 不能在 CTV 中产生 sgmRNA。