Hanson R S, Chilton M D
J Bacteriol. 1975 Dec;124(3):1220-6. doi: 10.1128/jb.124.3.1220-1226.1975.
Treatment of tomato plants with Agrobacterium tumefaciens causes subsequently administered [3H]thymidine to be preferentially incorporated into a satellite deoxyribonucleic acid (DNA) whose buoyant density is between that of bacterial DNA (rho = 1.718 g/cm3) and plant main band DNA (rho = 1.692 g/cm3). Satellite DNA upon shearing or sonic treatment releases fragments of higher and lower buoyant density, as reported by earlier investigators. The satellite has no significant base sequence homology with A. tumefaciens DNA, for its rate of reassociation is not accelerated by the addition of high concentrations of the latter. Tomato DNA isolated from shoots or from leaf nuclei accelerates renaturation of labeled satellite DNA. We conclude that the intermediate density labeled DNA is a plant satellite and not the product of covalent joining of bacterial and plant DNA as suggested by earlier investigators.
用根癌土壤杆菌处理番茄植株,会使随后施用的[3H]胸腺嘧啶优先掺入一种卫星脱氧核糖核酸(DNA)中,该卫星DNA的浮力密度介于细菌DNA(ρ = 1.718 g/cm³)和植物主带DNA(ρ = 1.692 g/cm³)之间。如早期研究人员所报道,卫星DNA经剪切或超声处理后会释放出浮力密度较高和较低的片段。该卫星与根癌土壤杆菌DNA没有明显的碱基序列同源性,因为添加高浓度的后者并不会加速其复性速率。从芽或叶核中分离出的番茄DNA会加速标记卫星DNA的复性。我们得出结论,中等密度的标记DNA是一种植物卫星DNA,而不是如早期研究人员所认为的那样,是细菌和植物DNA共价连接的产物。