Wolfes H, Fliess A, Pingoud A
Eur J Biochem. 1985 Jul 1;150(1):105-10. doi: 10.1111/j.1432-1033.1985.tb08994.x.
We have investigated the structural requirements for DNA cleavage by the isoschizomers HaeIII, BspRI and BsuRI which recognize the sequence -d(GGCC)-. For this purpose decadeoxynucleotides were synthesized by the solid-phase phosphotriester method and purified by high-performance liquid chromatography. The kinetics of cleavage of these oligodeoxynucleotides were determined for the three isoschizomers with the following results. The sequence adjacent to the recognition site strongly influences the rate of cleavage. The preference is qualitatively the same for all three enzymes: AGGCCT greater than TGGCCA greater than GGGCCC approximately equal to CGGCCG, and follows the thermal stability of the different decanucleotides. Substitutions within the recognition site, namely dI for dG and dU for dC, affect the rate of cleavage differently for the three enzymes. The results can be rationalized in terms of an interaction of HaeIII with the major and minor groove of the DNA, of BspRI mainly with the minor groove and of BsuRI with the major groove of DNA. It is obvious from our data that the mechanism of recognition of the same site is different for the three isoschizomers.
我们研究了识别序列-d(GGCC)-的同裂酶HaeIII、BspRI和BsuRI切割DNA的结构要求。为此,采用固相磷酸三酯法合成了十聚脱氧核苷酸,并通过高效液相色谱法进行纯化。测定了这三种同裂酶对这些寡脱氧核苷酸的切割动力学,结果如下。识别位点相邻的序列强烈影响切割速率。所有三种酶的偏好性在定性上是相同的:AGGCCT大于TGGCCA大于GGGCCC约等于CGGCCG,并且与不同十聚核苷酸的热稳定性一致。识别位点内的取代,即dI取代dG和dU取代dC,对这三种酶的切割速率影响不同。根据HaeIII与DNA大沟和小沟的相互作用、BspRI主要与小沟的相互作用以及BsuRI与DNA大沟的相互作用,可以对结果进行合理解释。从我们的数据可以明显看出,这三种同裂酶识别相同位点的机制是不同的。