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克隆于超螺旋质粒中的交替嘌呤-嘧啶反向重复序列的结构相互转换。

Structural interconversion of alternating purine-pyrimidine inverted repeats cloned in supercoiled plasmids.

作者信息

Klysik J, Zacharias W, Galazka G, Kwinkowski M, Uznanski B, Okruszek A

机构信息

Department of Bioorganic Chemistry, Polish Academy of Sciences, Lodz.

出版信息

Nucleic Acids Res. 1988 Jul 25;16(14B):6915-33. doi: 10.1093/nar/16.14.6915.

Abstract

Two self complementary oligonucleotides, T(GC)4AT(GC)4ACATG and C(GC)2(AT)5 (GC)3ATG, were synthesized and cloned into plasmids. Negative supercoiling causes a structural transition in the primary helix of both inserts. The first sequence converts into the left-handed helix, whereas the second sequence undergoes a transition into a cruciform or a Z-type structure depending on the experimental conditions employed. This has been deduced from the mapping of S1 nuclease sensitive sites, OsO4-sensitive sites, DEP modification pattern and relaxation studies. In addition, the differential effect of 5-cytosine methylation and binding of the AT-specific drug distamycin on these transitions further supports this interpretation. Thus, it is demonstrated, that the same sequence which is both inverted repeat and alternating purine-pyrimidine type may adopt either the left-handed conformation or the cruciform structure in response to the superhelical stress. Formation of the Z-type helix can be transmitted through the d(AT)n region which is 10 bp in length.

摘要

合成了两条自我互补的寡核苷酸,即T(GC)4AT(GC)4ACATG和C(GC)2(AT)5(GC)3ATG,并将它们克隆到质粒中。负超螺旋导致两个插入片段的一级螺旋发生结构转变。第一个序列转变为左手螺旋,而第二个序列根据所采用的实验条件转变为十字形或Z型结构。这是通过S1核酸酶敏感位点、锇酸(OsO4)敏感位点、DEP修饰模式和松弛研究的图谱推导出来的。此外,5-胞嘧啶甲基化和AT特异性药物偏端霉素结合对这些转变的差异效应进一步支持了这一解释。因此,证明了相同的既是反向重复又是嘌呤-嘧啶交替类型的序列可响应超螺旋应力而采用左手构象或十字形结构。Z型螺旋的形成可通过长度为10 bp的d(AT)n区域传递。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cf3/338342/6e2d8324545d/nar00168-0233-a.jpg

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