Guerineau M, Grandchamp C, Slonimski P P
Proc Natl Acad Sci U S A. 1976 Sep;73(9):3030-4. doi: 10.1073/pnas.73.9.3030.
Small circular DNA molecules from genetically characterized clones of Saccharomyces cerevisiae have been studied by restriction endonuclease analysis and electron microscopy. The circular monomers (6000 bases) are shown to contain two inverted repeats of the same sequence (600 bases) situated opposite each other along the perimeter. Four endonuclease EcoRI fragments are obtained in 1:1:1:1 stoichiometry, and their sum gives a length of about 12,000 bases. The two large fragments and the two small ones differ from each other by 200 bases. We propose a model for the structure of the monomer molecule. Two classes of monomers can be generated by intramolecular recombinations within inverted repeats; they differ by the relative orientation of nonrepeated segments. The structure of dimers as predicted by the model is verified by self-renaturation of single-stranded circles. Inverted repeats in circular molecules may be related to the insertion release faculty of II episome in the chromosomes.
通过限制性内切酶分析和电子显微镜对来自基因特征明确的酿酒酵母克隆的小环状DNA分子进行了研究。环状单体(6000个碱基)显示沿周长含有两个彼此相对的相同序列(600个碱基)的反向重复序列。以1:1:1:1的化学计量比获得四个内切酶EcoRI片段,它们的总和给出约12000个碱基的长度。两个大片段和两个小片段相差200个碱基。我们提出了单体分子结构的模型。两类单体可通过反向重复序列内的分子内重组产生;它们因非重复片段的相对取向而异。该模型预测的二聚体结构通过单链环的自我复性得到验证。环状分子中的反向重复序列可能与II型附加体在染色体中的插入释放能力有关。