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首页> 外文期刊>Nucleic acids research >Double-stranded cucumovirus associated RNA 5: which sequence variations may be detected by optical melting and temperature-gradient gel electrophoresis?
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Double-stranded cucumovirus associated RNA 5: which sequence variations may be detected by optical melting and temperature-gradient gel electrophoresis?

机译:双链cucumovirus相关的RNA 5:可以通过光学熔解和温度梯度凝胶电泳检测哪些序列变异?

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Sequence variants of the double-stranded form of satellite RNAs of cucumber mosaic virus (dsCARNA 5) were analyzed for the possibility to experimentally detect minor nucleotide sequence changes. Denaturation maps (helix-probability versus position of the nucleotide in the sequence versus temperature) were calculated applying the Poland algorithm. Optical denaturation curves and temperature-gradient gel mobility curves were simulated using the denaturation maps and were compared with experimental results from optical melting and temperature-gradient gel electrophoresis (Tien Po et al., accompanying paper). Melting of the dsRNAs starts from both ends of the molecule in two transitions of low co-operativity, continues in the right part in a highly co-operative transition, and is finished in another highly co-operative transition including strand-separation. Whereas all parts of the molecule contribute uniformly to the optical melting curve, opening of the ends predominates in the retardation transition in gel electrophoresis. Detailed discussion of the influence of base pair changes in the sequence shows that a single base pair change may be detected by temperature-gradient gel electrophoresis, if it is located in certain favorable locations, whereas its detection in optical melting curves is possible only in very special cases. The systematic differences found in the accompanying paper between necrogenic and non-necrogenic dsCARNA 5 could be interpreted on the basis of such nucleotide sequence differences.
机译:分析了黄瓜花叶病毒(dsCARNA 5)卫星RNA双链形式的序列变体,以通过实验检测较小的核苷酸序列变化的可能性。使用波兰算法计算变性图(螺旋概率与序列中核苷酸的位置与温度)。使用变性图模拟光学变性曲线和温度梯度凝胶迁移率曲线,并将其与光学熔融和温度梯度凝胶电泳的实验结果进行比较(Tien Po等人,随附论文)。 dsRNA的熔解从分子的两端开始,在两个低协作性的过渡中开始,在右侧的高度合作性过渡中继续,并在另一个高度合作的过渡中完成,包括链分离。尽管分子的所有部分均对光学熔解曲线均匀地起作用,但在凝胶电泳的延迟转变中,末端的开放占主导。对碱基对变化顺序的影响的详细讨论表明,如果单个碱基对变化位于某些有利位置,则可以通过温度梯度凝胶电泳检测到,而仅在非常高的熔解曲线中可以检测到该变化。特别案例。可以根据此类核苷酸序列差异来解释在随附论文中发现的致死性和非致死性dsCARNA 5之间的系统差异。

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