首页> 美国卫生研究院文献>Nucleic Acids Research >S1-sensitive sites in the supercoiled double-stranded form of tomato golden mosaic virus DNA component B: identification of regions of potential alternative secondary structure and regulatory function.
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S1-sensitive sites in the supercoiled double-stranded form of tomato golden mosaic virus DNA component B: identification of regions of potential alternative secondary structure and regulatory function.

机译:番茄金色花叶病毒DNA组分B的超螺旋双链形式中的S1敏感位点:识别潜在的替代二级结构和调节功能的区域。

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摘要

The sensitivity of the supercoiled double-stranded form of the DNA of tomato golden mosaic virus (TGMV), a geminivirus, to the single-strand specific enzyme S1 nuclease has been demonstrated. Specific S1 cleavage sites were identified in TGMV DNA component B by cloning into the single-strand bacteriophage vector M13 mp8 and sequencing of the inserted DNA. Analysis of the DNA sequence at the sites of S1 sensitivity in TGMV DNA component B revealed several possible regions of alternative secondary structure which were clustered in an intergenic region upstream of the starts of the two major open reading frames which are in opposite orientations. This region contains putative transcriptional promoter and modulatory sequences and a possible replication origin. The extreme S1 sensitivity of the supercoiled form of TGMV DNA component A precluded its cloning under the conditions employed for selective cleavage of DNA component B.
机译:已经证明了双链形式的番茄金黄色花叶病毒(TGMV)(双生病毒)的DNA对单链特异性酶S1核酸酶的敏感性。通过克隆到单链噬菌体载体M13 mp8中并对插入的DNA进行测序,在TGMV DNA组分B中鉴定出特定的S1切割位点。 TGMV DNA组分B中S1敏感性位点的DNA序列分析揭示了一些可能的二级结构可能区域,这些区域聚集在两个主要开放阅读框起始方向相反的上游基因间区域中。该区域包含推定的转录启动子和调节序列以及可能的复制起点。 TGMV DNA组分A的超螺旋形式具有极高的S1敏感性,因此无法在选择性切割DNA组分B的条件下进行克隆。

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