Meyerink J H, Retèl J
Nucleic Acids Res. 1976 Oct;3(10):2697-707. doi: 10.1093/nar/3.10.2697.
Yeast ribosomal DNA (rDNA) was digested with the restriction endonuclease EcoRI. Eight distinct fragments were obtained with a molecular weight of 4.35 (1), 1.75 (2), 1.45 (3), 1.07 (4), 0.42 (5), 0.37 (6), 0.26 (7) and 0.22 x 10(6) (8) daltons, respectively. Except for fragment 1 with a molecular weight of 4.35 x 10(6) daltons, all fragments are derived from the multiple ribosomal transcription units. The 'spacer' sequences, on the other hand, gave rise to digestion products which are very heterogeneous in size. By analysis of the partial digestion products which are very heterogeneous in size. By analysis of the partial digestion products, together with the data obtained by digestion with a combination of two restriction enzymes (EcoRI and Hind II or Hind III) and redigestion of the Hind II-and Hind III-fragments with EcoRI, the physical map of the EcoRI cleavage sites in the ribosomal transcription unit could be established.
用限制性内切酶EcoRI消化酵母核糖体DNA(rDNA)。得到了八个不同的片段,分子量分别为4.35(1)、1.75(2)、1.45(3)、1.07(4)、0.42(5)、0.37(6)、0.26(7)和0.22×10⁶(8)道尔顿。除了分子量为4.35×10⁶道尔顿的片段1外,所有片段均来自多个核糖体转录单元。另一方面,“间隔区”序列产生了大小非常不均一的消化产物。通过对大小非常不均一的部分消化产物进行分析。通过分析部分消化产物,结合用两种限制性酶(EcoRI和Hind II或Hind III)组合消化以及用EcoRI对Hind II和Hind III片段进行再消化得到的数据,可以建立核糖体转录单元中EcoRI切割位点的物理图谱。