Grdzelishvili V Z, Chapman S N, Dawson W O, Lewandowski D J
Department of Plant Pathology, CREC, University of Florida, Lake Alfred, Florida 33850, USA.
Virology. 2000 Sep 15;275(1):177-92. doi: 10.1006/viro.2000.0511.
The Tobacco mosaic virus movement protein (MP) and coat protein (CP) are expressed from 3'-coterminal subgenomic RNAs (sgRNAs). The transcription start site of the MP sgRNA, previously mapped to positions 4838 (Y. Watanabe, T. Meshi, and Y. Okada (1984), FEBS Lett. 173, 247-250) and 4828 (K. Lehto, G. L. Grantham, and W. O. Dawson (1990), Virology 174, 145-157) for the TMV OM and U1 strains, respectively, has been reexamined and mapped to position 4838 for strain U1. Sequences of the MP and CP sgRNA promoters were delineated by deletion analysis. The boundaries for minimal and full MP sgRNA promoter activity were localized between -35 and +10 and -95 and +40, respectively, relative to the transcription start site. The minimal CP sgRNA promoter was mapped between -69 and +12, whereas the boundaries of the fully active promoter were between -157 and +54. Computer analysis predicted two stem-loop structures (SL1 and SL2) upstream of the MP sgRNA transcription start site. Deletion analysis and site-directed mutagenesis suggested that SL1 secondary structure, but not its sequence, was required for MP sgRNA promoter activity, whereas a 39-nt deletion removing most of the SL2 region increased MP sgRNA accumulation fourfold. Computer-predicted folding of the fully active CP sgRNA promoter revealed one long stem-loop structure. Deletion analysis suggested that the upper part of this stem-loop, located upstream of the transcription start site, was essential for transcription and that the lower part of the stem had an enhancing role.
烟草花叶病毒运动蛋白(MP)和外壳蛋白(CP)由3' 共末端亚基因组RNA(sgRNA)表达。MP sgRNA的转录起始位点,先前已分别定位到烟草花叶病毒OM株的4838位(Y. 渡边、T. 梅西和Y. 冈田(1984年),《欧洲生物化学学会联合会快报》173,247 - 250)和U1株的4828位(K. 莱托、G. L. 格兰瑟姆和W. O. 道森(1990年),《病毒学》174,145 - 157),现已重新研究并将U1株的转录起始位点定位到4838位。通过缺失分析确定了MP和CP sgRNA启动子的序列。相对于转录起始位点,最小和完整MP sgRNA启动子活性的边界分别定位在 - 35至 + 10和 - 95至 + 40之间。最小CP sgRNA启动子定位在 - 69至 + 12之间,而完全活性启动子的边界在 - 157至 + 54之间。计算机分析预测在MP sgRNA转录起始位点上游有两个茎环结构(SL1和SL2)。缺失分析和定点诱变表明,MP sgRNA启动子活性需要SL1二级结构,但不需要其序列,而去除大部分SL2区域的39个核苷酸缺失使MP sgRNA积累增加了四倍。完全活性CP sgRNA启动子的计算机预测折叠显示有一个长茎环结构。缺失分析表明,这个茎环位于转录起始位点上游的上部对转录至关重要,而茎的下部有增强作用。