The Biological Laboratories, Harvard University, 02138, Cambridge, MA, USA.
Plant Mol Biol. 1983 May;2(3):129-40. doi: 10.1007/BF01578513.
Fragments produced by partial digestion of plastid DNA fromZea mays withEco RI were cloned in Charon 4A. A circular, fine structure physical map of the plastid DNA was then constructed from restriction endonucleaseSal I,Pst I,Eco RI, andBam HI recognition site maps of cloned overlapping segments of the plastid genome. These fragments were assigned molecular weights by reference to size markers from both pBR322 and lambda phage DNA. Because of the detail and extent of the derived map, it has been possible to construct a coordinate system which has a unique zero point and within which all the restriction fragments and previously described structural features can be mapped. A computer program was constructed which will display in a circular fashion any of the above features using an X-Y plotter.
用EcoRI 部分消化来自玉米质体 DNA 产生的片段被克隆到 Charon 4A 中。然后,根据克隆的质体基因组重叠片段的限制内切酶 Sal I、Pst I、EcoRI 和 BamHI 识别位点图谱,构建了质体 DNA 的圆形精细结构物理图谱。这些片段通过参考 pBR322 和 lambda 噬菌体 DNA 的大小标记来指定分子量。由于衍生图谱的详细程度和范围,已经可以构建一个具有唯一零点的坐标系,在此坐标系中可以映射所有限制片段和先前描述的结构特征。构建了一个计算机程序,该程序可以使用 X-Y 绘图仪以圆形方式显示上述任何特征。