首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Identity of the 5′-Terminal RNA Nucleotide Sequence of the Satellite Tobacco Necrosis Virus and Its Helper Virus: Possible Role of the 5′-Terminus in the Recognition by Virus-Specific RNA Replicase
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Identity of the 5′-Terminal RNA Nucleotide Sequence of the Satellite Tobacco Necrosis Virus and Its Helper Virus: Possible Role of the 5′-Terminus in the Recognition by Virus-Specific RNA Replicase

机译:卫星烟草坏死病毒及其辅助病毒的5-末端RNA核苷酸序列的同一性:5-末端在病毒特异性RNA复制酶识别中的可能作用

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摘要

A pancreatic ribonuclease digest of 14C-labeled tobacco necrosis virus RNA was fractionated according to charge by column chromatography. Individual fractions were dephosphorylated with alkaline phosphatase and rechromatographed. The fraction, originally containing oligonucleotides with seven negative charges, separated into two components corresponding to five (-5) and two negative charges (-2). The -5 fraction was derived from the internal oligonucleotides while the -2 fraction must have originated from a 5′-pyrophosphorylated terminal trinucleotide. The sequence of this terminal trinucleotide was determined by column chromatography on DEAE-cellulose in a triethyl ammonium carbonate gradient, using the appropriate markers. The radioactivity chromatographed with a (ApGp)U marker. The order of the Ap and Gp was determined after ribonuclease T1 and alkaline phosphatase digestion. The radioactivity in the product chromatographed with an ApG marker. The 5′-terminus of tobacco necrosis virus RNA was therefore determined as ppApGpUp..., which is identical to the terminus of the RNA of its satellite virus as previously determined (J. Mol. Biol., 38, 59 (1968); Science, 160, 1452 (1968)). The 5′ pyrophosphate in both viruses was probably formed by an in vivo enzymatic removal of a γ-phosphate from a triphosphate, and its presence in both viruses suggested a common site of synthesis. The identity of the 5′-terminal sequences is considered not to be fortuitous and is discussed from the standpoint of their role as a recognition site for the virus-specific RNA replicase.
机译:通过柱色谱法根据电荷分离出 14 C标记的烟草坏死病毒RNA的胰核糖核酸酶消化物。各个级分用碱性磷酸酶脱磷酸并重新层析。该部分最初包含具有七个负电荷的寡核苷酸,分为两个成分,分别对应于五个(-5)和两个负电荷(-2)。 -5馏分源自内部寡核苷酸,而-2馏分必须源自5'-焦磷酸化的末端三核苷酸。使用合适的标记,通过柱色谱在DEAE-纤维素上以碳酸三乙铵的梯度确定该末端三核苷酸的序列。用(ApGp)U标记进行放射色谱分析。在核糖核酸酶T1和碱性磷酸酶消化后,确定Ap和Gp的顺序。用ApG标记色谱分离的产品中的放射性。因此,将烟草坏死病毒RNA的5'末端确定为ppApGpUp ...,其与先前确定的其卫星病毒的RNA末端相同(J. Mol。Biol。,38,59(1968); Science,160,1452(1968))。两种病毒中的5'焦磷酸盐可能是通过体内从三磷酸盐中酶法去除γ-磷酸盐而形成的,并且它在两种病毒中的存在都表明存在一个共同的合成位点。 5'-末端序列的同一性被认为不是偶然的,并且从它们作为病毒特异性RNA复制酶的识别位点的作用的角度进行了讨论。

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