Hayakawa T, Ono A, Ueda T
Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Nucleic Acids Res. 1988 Jun 10;16(11):4761-76. doi: 10.1093/nar/16.11.4761.
Decadeoxyribonucleotides containing uracil, 5-bromouracil, 5-cyanouracil and 5-ethyluracil in recognition sequences of restriction endonucleases Bgl II, Sau 3AI, Mbo I were synthesized. Decanucleotides containing 5-bromouracil in place of thymine had essentially the same susceptibility to all the restriction endonucleases. Uracil-containing decanucleotides were however very resistant to attack. Decanucleotides containing 5-cyanouracil in the recognition sequence were strongly resistant to hydrolysis by Sau 3AI, but were hydrolysed by Bgl II and Mbo I as well as the parent decanucleotide. Decanucleotides containing 5-ethyluracil were strongly resistant to hydrolysis by Sau 3AI, but were partially resistant to hydrolysis by Bgl II and Mbo I.
合成了在限制性内切酶Bgl II、Sau 3AI、Mbo I识别序列中含有尿嘧啶、5-溴尿嘧啶、5-氰基尿嘧啶和5-乙基尿嘧啶的十脱氧核糖核苷酸。用5-溴尿嘧啶取代胸腺嘧啶的十核苷酸对所有限制性内切酶的敏感性基本相同。然而,含尿嘧啶的十核苷酸对酶切作用具有很强的抗性。识别序列中含有5-氰基尿嘧啶的十核苷酸对Sau 3AI的水解作用具有很强的抗性,但能被Bgl II、Mbo I以及亲本十核苷酸水解。含有5-乙基尿嘧啶的十核苷酸对Sau 3AI的水解作用具有很强的抗性,但对Bgl II和Mbo I的水解作用具有部分抗性。