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单链DNA的非酶促序列特异性切割

Nonenzymatic sequence-specific cleavage of single-stranded DNA.

作者信息

Chu B C, Orgel L E

出版信息

Proc Natl Acad Sci U S A. 1985 Feb;82(4):963-7. doi: 10.1073/pnas.82.4.963.

Abstract

Ethylenediaminetetraacetic acid and diethylenetriaminepentaacetic acid have been attached covalently to the 5' terminus of the deoxynucleotide sequence C-A-C-A-A-T-T-C-C-A-C-A-C-A-A-C (16-mer) via an ethylenediamine linker. In the presence of Fe2+ and dithiothreitol, these reagents bring about the hybridization-dependent cleavage of the sequence T-C-G-T-A-T-G-T-T-G-T-G-T-G-G-A-A-T-T-G-T-G-A-G-C-G-G-A-T-A-A-C-A-A-T-T- T (37-mer), a sequence that contains an internal subsequence complementary to the 16-mer. The principal cleavage sites on the 37-mer are about four residues on each side of the terminal phosphate group of the 16-mer.

摘要

乙二胺四乙酸和二乙烯三胺五乙酸已通过乙二胺连接体共价连接到脱氧核苷酸序列C-A-C-A-A-T-T-C-C-A-C-A-C-A-A-C(16聚体)的5'末端。在Fe2+和二硫苏糖醇存在的情况下,这些试剂会导致序列T-C-G-T-A-T-G-T-T-G-T-G-T-G-G-A-A-T-T-G-T-G-A-G-C-G-G-A-T-A-A-C-A-A-T-T-T(37聚体)发生杂交依赖性切割,该序列包含与16聚体互补的内部子序列。37聚体上的主要切割位点位于16聚体末端磷酸基团两侧各约四个残基处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c3f/397173/2fe20df152db/pnas00344-0018-a.jpg

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