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应激诱导克隆的d(CATG)10序列中十字形结构的形成。

Stress-induced cruciform formation in a cloned d(CATG)10 sequence.

作者信息

Naylor L H, Lilley D M, van de Sande J H

出版信息

EMBO J. 1986 Sep;5(9):2407-13. doi: 10.1002/j.1460-2075.1986.tb04511.x.

Abstract

The synthetic alternating purine-pyrimidine sequence, d(CATG)10.d(CATG)10, has been cloned into a 2.079-kb pBR322-derived plasmid (pLN1) and its conformation studied under torsional stress. The resultant plasmid, pLNc40, is hypersensitive to cleavage by the single strand-specific nucleases, S1 nuclease and Bal31 nuclease, and to modification by the single strand-selective reagent, osmium tetroxide. The S1-hypersensitive site of this plasmid predominates over those previously mapped in pBR322. Site-specific cleavage of pLNc40 with the resolvase T4 endonuclease VII demonstrates that this alternating purine-pyrimidine tract selectively forms a cruciform structure when stably integrated into a negatively supercoiled plasmid. Quantitative measurements of the twist change (-4.3 +/- 0.2) and free energy of formation (16.2 +/- 0.5 kcal/mol) of this cruciform have been made from two-dimensional gel electrophoresis experiments, and correspond well with the predicted values of cruciform formation for this sequence. We conclude that cruciform extrusion versus the B-Z transition is the favoured conformation of this insert under torsional stress.

摘要

合成的交替嘌呤-嘧啶序列d(CATG)10.d(CATG)10已被克隆到一个2.079 kb的pBR322衍生质粒(pLN1)中,并在扭转应力下研究其构象。所得质粒pLNc40对单链特异性核酸酶S1核酸酶和Bal31核酸酶的切割以及单链选择性试剂四氧化锇的修饰高度敏感。该质粒的S1超敏位点比先前在pBR322中定位的位点更占优势。用解离酶T4内切核酸酶VII对pLNc40进行位点特异性切割表明,当该交替嘌呤-嘧啶片段稳定整合到负超螺旋质粒中时,它选择性地形成十字形结构。通过二维凝胶电泳实验对该十字形结构的扭曲变化(-4.3±0.2)和形成自由能(16.2±0.5 kcal/mol)进行了定量测量,与该序列十字形形成的预测值非常吻合。我们得出结论,在扭转应力下,十字形挤出相对于B-Z转变是该插入片段的有利构象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e61/1167127/424f70bba1ae/emboj00172-0360-a.jpg

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