Kim J, Zwieb C, Wu C, Adhya S
Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Gene. 1989 Dec 21;85(1):15-23. doi: 10.1016/0378-1119(89)90459-9.
The binding of a protein to its specific sequence, borne on a DNA fragment, retards the mobility of the fragment in a characteristic way during gel electrophoresis. If the protein induces bending in the DNA, the contortion can also be monitored by gel electrophoresis, because the amount of retardation of the mobility of the DNA-protein complex is dependent upon the position and the degree of the bend induced in the DNA fragment [Wu and Crothers, Nature 308 (1984) 509-513]. We have constructed a plasmid, pBend2, which can generate a large number of DNA fragments of identical length in which the protein-binding nucleotide sequence is located in circular permutations. The vector contains two identical DNA segments containing 17 restriction sites in a direct repeat spanning a central region containing cloning sites. The protein-binding sequence is inserted at one of these cloning sites. To investigate the functional significance of bending, we have compared, using pBend2, the cAMP.cAMP-receptor protein (CPR)-induced bending of CRP-binding sites found in five different genes of Escherichia coli. We have also shown that the bacteriophage lambda 0R1 operator DNA is bent when complexed with the CI or Cro repressor of the phage.
蛋白质与其特定序列(位于DNA片段上)的结合,会在凝胶电泳过程中以一种独特的方式使该片段的迁移率降低。如果蛋白质诱导DNA发生弯曲,这种扭曲也可以通过凝胶电泳进行监测,因为DNA - 蛋白质复合物迁移率的降低程度取决于DNA片段中诱导弯曲的位置和程度[吴和克罗瑟斯,《自然》308 (1984) 509 - 513]。我们构建了一个质粒pBend2,它能产生大量长度相同的DNA片段,其中蛋白质结合核苷酸序列呈环状排列。该载体包含两个相同的DNA片段,在一个跨越包含克隆位点的中心区域的同向重复序列中有17个限制性酶切位点。蛋白质结合序列插入其中一个克隆位点。为了研究弯曲的功能意义,我们使用pBend2比较了在大肠杆菌五个不同基因中发现的cAMP - cAMP受体蛋白(CRP)诱导的CRP结合位点的弯曲情况。我们还表明,噬菌体λ 0R1操纵子DNA与噬菌体的CI或Cro阻遏蛋白结合时会发生弯曲。