Pritchard A E, Laskowski M
J Biol Chem. 1978 Nov 25;253(22):7989-92.
A single strand specific endonuclease, venom phosphodiesterase, acting on superhelical phiX174 DNA, inflicts at least seven specific cleavages. Six of these were located to within approximately +/-40 base-pairs by mapping with restriction endonucleases. They are at 12%, 27.4%, 42.7%, 47.5%, 76.1%, and 82.5%. All of these sites lie within regions containing runs of 16 or more base-pairs, of which 12 or more are A and T. Other similarly (A + T)-rich regions in the genome are not cleaved by the enzyme. Increasing the superhelical density of the substrate did not alter the locations of the cleavage sites. There is no correlation between the locations of the cleavage sites and the three known major promoter sites. Only two of five postulated transcription termination sites are cleaved by phosphodiesterase even though all of these terminators contain (A + T)-rich regions. The area containing the origin of viral DNA replication, which includes an (A + T)-rich sequence, is not cleaved.
一种单链特异性核酸内切酶——蛇毒磷酸二酯酶,作用于超螺旋φX174 DNA时,会造成至少七个特异性切割位点。通过用限制性内切酶进行图谱分析,其中六个切割位点位于大约±40个碱基对范围内。它们分别位于12%、27.4%、42.7%、47.5%、76.1%和82.5%处。所有这些位点都位于包含16个或更多碱基对的区域内,其中12个或更多是A和T。基因组中其他类似富含(A + T)的区域不会被该酶切割。增加底物的超螺旋密度不会改变切割位点的位置。切割位点的位置与三个已知的主要启动子位点之间没有相关性。尽管所有这些终止子都包含富含(A + T)的区域,但五个假定的转录终止位点中只有两个会被磷酸二酯酶切割。包含病毒DNA复制起点的区域,其中包括一个富含(A + T)的序列,不会被切割。