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利用T4连接酶恢复对“平齐”切割限制酶敏感的DNA序列。

Restoration by T4 ligase of DNA sequences sensitive to "flush" cleaving restriction enzyme.

作者信息

Mottes M, Morandi C, Cremaschi S, Sgaramella V

出版信息

Nucleic Acids Res. 1977 Jul;4(7):2467-75. doi: 10.1093/nar/4.7.2467.

Abstract

Fouteen "flush"-ended segments originate from the action of the restriction endonuclease Hae III of Haemophilus aegiptius on the DNA of the colicinogenic factor ColE 1 (A. Oka and M. Takanami, Nature, 264, 191, 1976). They are joined by the T4 polynucleotide ligase. The reaction can be monitored by gel electrophoresis, electron microscopy and resistance to phosphatase of the 5'-32P labelled ends. The joined products are a random recombination of the original segments, and can be cleaved by the same Hae III endonuclease to restore the exact electrophoretic pattern of the Hae III-cut ColE 1 DNA. In a properly diluted mixture of 5'-32P segments treated with T4 ligase, the level of phosphatase resistance is very close to the frequency of circle-formation as determined by electron microscopy: thus, the joining of the "flush"-ends involves the formation of circular structures covalently closed in both strands.

摘要

14个“平端”片段源自埃及嗜血杆菌的限制性内切酶Hae III对产大肠杆菌素因子ColE 1的DNA的作用(A. 冈和M. 高波,《自然》,第264卷,第191页,1976年)。它们由T4多核苷酸连接酶连接。该反应可通过凝胶电泳、电子显微镜以及对5'-32P标记末端的磷酸酶抗性进行监测。连接产物是原始片段的随机重组,并且可以被相同的Hae III内切酶切割,以恢复Hae III切割的ColE 1 DNA的精确电泳图谱。在用T4连接酶处理的5'-32P片段的适当稀释混合物中,磷酸酶抗性水平非常接近通过电子显微镜确定的环形成频率:因此,“平端”的连接涉及在两条链中均共价闭合的环状结构的形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8522/342579/2c7d8b478466/nar00480-0359-a.jpg

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