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双链黄瓜花叶病毒相关RNA 5:通过光熔解和温度梯度凝胶电泳可检测到哪些序列变异?

Double-stranded cucumovirus associated RNA 5: which sequence variations may be detected by optical melting and temperature-gradient gel electrophoresis?

作者信息

Steger G, Po T, Kaper J, Riesner D

出版信息

Nucleic Acids Res. 1987 Jul 10;15(13):5085-103. doi: 10.1093/nar/15.13.5085.

Abstract

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.

摘要

对黄瓜花叶病毒双链形式卫星RNA(dsCARNA 5)的序列变体进行了分析,以探讨通过实验检测微小核苷酸序列变化的可能性。应用波兰算法计算了变性图谱(螺旋概率与序列中核苷酸位置及温度的关系)。利用变性图谱模拟了光学变性曲线和温度梯度凝胶迁移率曲线,并与光学熔解和温度梯度凝胶电泳的实验结果进行了比较(田波等人,附文)。dsRNA的熔解从分子的两端开始,经历两个低协同性的转变,在右侧部分以高度协同的转变继续进行,并在另一个包括链分离的高度协同转变中结束。虽然分子的所有部分对光学熔解曲线的贡献是均匀的,但在凝胶电泳的延迟转变中,末端的打开占主导地位。对序列中碱基对变化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,而只有在非常特殊的情况下才能在光学熔解曲线中检测到。附文中在致坏死性和非致坏死性dsCARNA 5之间发现的系统差异可以基于此类核苷酸序列差异来解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/025f/305949/c0156613d7be/nar00257-0104-a.jpg

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