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d(CA/TG)n的非B-DNA结构不同于Z-DNA的结构。

The non-B-DNA structure of d(CA/TG)n differs from that of Z-DNA.

作者信息

Kladde M P, Kohwi Y, Kohwi-Shigematsu T, Gorski J

机构信息

Department of Biochemistry, University of Wisconsin, Madison 53706.

出版信息

Proc Natl Acad Sci U S A. 1994 Mar 1;91(5):1898-902. doi: 10.1073/pnas.91.5.1898.

DOI:10.1073/pnas.91.5.1898
PMID:8127902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC43271/
Abstract

Chemical probing of two predominantly alternating purine-pyrimidine d(CA/TG)n repeats led us to propose previously that in supercoiled plasmids these elements adopt a non-B-DNA structure distinct from that of Z-DNA formed by d(CG)n sequences. Here, we present further evidence supporting this contention. Reactivity with the conformation-sensitive reagent chloroacetaldehyde, which reacts with unpaired adenines and cytosines, was confined strictly to adenines in the d(CA/TG)n repeat. In contrast, only bases outside the d(CG)n repeat exhibited chloroacetaldehyde reactivity. Two-dimensional gel analysis of topoisomers containing d(CA/TG)n tracts with bases out of strict purine-pyrimidine alteration revealed multiple superhelical-dependent transitions to an alternative left-handed structure. Within individual plasmid molecules, these multiple transitions resulted from the stepwise conversion of contiguous segments of alternating purine-pyrimidine sequence, which are delimited by bases out of alternation, to the full-length alternative conformation. When the left-handed helices increased in length to include more bases out of alternation, the average helical pitch changed substantially to produce a less tightly wound left-handed helix. Overall, these data indicate that d(CA/TG)n tracts adopt a left-handed conformation significantly different from that of the canonical Z-DNA structure of d(CG)n sequences.

摘要

对两个主要为交替嘌呤 - 嘧啶的d(CA/TG)n重复序列进行化学探测,使我们先前提出,在超螺旋质粒中,这些元件采用一种不同于由d(CG)n序列形成的Z - DNA的非B - DNA结构。在此,我们提供进一步的证据支持这一论点。与构象敏感试剂氯乙醛的反应性,该试剂与未配对的腺嘌呤和胞嘧啶反应,严格局限于d(CA/TG)n重复序列中的腺嘌呤。相比之下,只有d(CG)n重复序列之外的碱基表现出氯乙醛反应性。对含有d(CA/TG)n片段且碱基偏离严格嘌呤 - 嘧啶交替的拓扑异构体进行二维凝胶分析,揭示了多个超螺旋依赖性转变为另一种左手结构。在单个质粒分子内,这些多个转变是由交替嘌呤 - 嘧啶序列的连续片段逐步转化导致的,这些片段由偏离交替的碱基界定,转化为全长的替代构象。当左手螺旋长度增加以包含更多偏离交替的碱基时,平均螺旋螺距发生显著变化,产生一个缠绕较松的左手螺旋。总体而言,这些数据表明d(CA/TG)n片段采用一种与d(CG)n序列的经典Z - DNA结构显著不同的左手构象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7c3/43271/8107777d5368/pnas01127-0311-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7c3/43271/715182f9e8a7/pnas01127-0309-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7c3/43271/a54a60b8b1b6/pnas01127-0310-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7c3/43271/8107777d5368/pnas01127-0311-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7c3/43271/715182f9e8a7/pnas01127-0309-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7c3/43271/a54a60b8b1b6/pnas01127-0310-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7c3/43271/8107777d5368/pnas01127-0311-a.jpg

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