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Mapping of the Tobacco mosaic virus movement protein and coat protein subgenomic RNA promoters in vivo

机译:体内烟草花叶病毒运动蛋白和外壳蛋白亚基因组RNA启动子的定位

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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), FEES 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, bur 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 par? 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, (C) 2000 Academic Press. [References: 70]
机译:烟草花叶病毒运动蛋白(MP)和外壳蛋白(CP)从3'-共末端亚基因组RNA(sgRNA)表达。 MP sgRNA的转录起始位点,先前定位于位置4838(Y。Watanabe,T。Meshi和Y. Okada(1984),FEES Lett 173、247-250)和4828(K。Lehto,GL Grantham和分别对TMV OM和U1株的WO Dawson(1990),Virology 174,145-157)进行了重新检查,并将其定位于U1株的4838位。通过缺失分析描绘了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位于-35和+10和-95和+40之间。最小CP sgRNA启动子位于-69和+12之间,而完全活性启动子的边界位于-157和+54之间。计算机分析预测了MP sgRNA转录起始位点上游的两个茎环结构(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,而不是其序列,而MP-sgRNA启动子活性需要39-nt缺失,从而使MP sgRNA积累增加了四倍。计算机预测的完全活跃的CP sgRNA启动子的折叠揭示了一个长茎环结构。删除分析提示上限?此茎环的一部分(位于转录起始位点的上游)对于转录至关重要,并且茎下部具有增强作用,(C)2000 Academic Press。 [参考:70]

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