Lakritz N, Foglesong P D, Reddy M, Baum S, Hurwitz J, Bauer W R
J Virol. 1985 Mar;53(3):935-43. doi: 10.1128/JVI.53.3.935-943.1985.
Multiple DNA-dependent enzyme activities have been detected in highly purified preparations of a single-strand-specific nuclease from vaccinia virus. These enzyme preparations were extensively purified and characterized by using superhelical DNAs as substrates. In particular, the nuclease activity was monitored by the extent of conversion of supercoiled closed duplex DNA (DNA I) to nicked circular DNA (DNA II), which could subsequently be converted to duplex linear DNA (DNA III) by prolonged incubation with the enzyme. DNA species which were not substrates for the enzyme included relaxed closed duplex DNA, DNA II which had been prepared by nuclease S1 treatment or by photochemical nicking of DNA I, and DNA III. With plasmid pSM1 DNA as substrate, the extent of cleavage of DNA I to DNA II was found to increase with superhelix density above a threshold value of about -0.06. The linear reaction products were examined by gel electrophoresis after restriction enzyme digestion of the DNAs from plasmids pSM1 and pBR322 and of the viral DNAs from bacteriophage phi X174 (replicative form) and simian virus 40, and the map coordinate locations of the scissions were determined. These products were further examined by electron microscopy and by gel electrophoresis under denaturing conditions. Electron micrographs taken under partially denaturing conditions revealed molecules with terminal loops or hairpins such as would result from the introduction of cross-links at the cutting sites. These species exhibited snapback renaturation. The denaturing gel electrophoresis experiments revealed the appearance of new bands at locations consistent with terminal cross-linking. With pSM1 and pBR322 DNAs, this band was shown to contain DNA that was approximately twice the length of a linear single strand. The terminal regions of the cross-linked linear duplex reaction products were sensitive to nuclease S1 but insensitive to proteinase K, suggesting that the structure is a hairpin loop not maintained by a protein linker. A similar structure is found in mature vaccinia virus DNA.
在来自痘苗病毒的单链特异性核酸酶的高度纯化制剂中检测到了多种依赖DNA的酶活性。这些酶制剂经过广泛纯化,并以超螺旋DNA作为底物进行了表征。特别地,通过超螺旋闭环双链DNA(DNA I)转化为带切口的环状DNA(DNA II)的程度来监测核酸酶活性,随后通过与该酶长时间孵育,DNA II可转化为双链线性DNA(DNA III)。不是该酶底物的DNA种类包括松弛的闭环双链DNA、通过核酸酶S1处理或DNA I的光化学切口制备的DNA II以及DNA III。以质粒pSM1 DNA作为底物,发现当超螺旋密度高于约-0.06的阈值时,DNA I切割为DNA II的程度会增加。在对来自质粒pSM1和pBR322的DNA以及来自噬菌体phi X174(复制形式)和猿猴病毒40的病毒DNA进行限制性酶切消化后,通过凝胶电泳检查线性反应产物,并确定切割的图谱坐标位置。这些产物通过电子显微镜和变性条件下的凝胶电泳进一步检查。在部分变性条件下拍摄的电子显微照片显示出带有末端环或发夹的分子,这是由切割位点引入交联所导致的。这些分子表现出快速复性。变性凝胶电泳实验揭示了在与末端交联一致的位置出现新条带。对于pSM1和pBR322 DNA,该条带显示包含长度约为线性单链两倍的DNA。交联线性双链反应产物的末端区域对核酸酶S1敏感,但对蛋白酶K不敏感,这表明该结构是一个不由蛋白质连接子维持的发夹环。在成熟的痘苗病毒DNA中也发现了类似的结构。