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酵母染色质中天然交替d(TA)n序列的结构分析。

Analysis of the structure of a natural alternating d(TA)n sequence in yeast chromatin.

作者信息

Aranda A, Pérez-Ortín J E, Benham C J, Del Olmo M L

机构信息

Departamento de Bioquímica y Biología Molecular, Universitat de València and Instituto de Agroquímica y Tecnología de Alimentos, CSIC, Burjassot, Spain.

出版信息

Yeast. 1997 Mar 30;13(4):313-26. doi: 10.1002/(SICI)1097-0061(19970330)13:4<313::AID-YEA93>3.0.CO;2-8.

DOI:10.1002/(SICI)1097-0061(19970330)13:4<313::AID-YEA93>3.0.CO;2-8
PMID:9133735
Abstract

We address here the question of the in vivo structure of a natural alternating d(TA)n sequence found at the 3' region of the Saccharomyces cerevisiae FBP1 gene. This sequence consists of 13 TA pairs interrupted by a TT dinucleotide in the middle of the tract. Previous experiments with cruciform-specific nucleases S1 and Endonuclease VII demonstrated the presence in vitro of a cruciform in this region. We also showed this region to be part of a nuclease hypersensitive site flanked by nucleosomes in yeast chromatin. Here we demonstrate, by means of S1 in vivo footprinting, that in yeast plasmids also adopts in vivo a non B-DNA structure where is not a cruciform. A theoretical analysis of this region that it contains a site susceptible to superhelical stress duplex destabilization. The locations and conditions under which alternative structures form in the wild-type sequence and in deletion mutants agree with these theoretical predictions, suggesting that some kind of denaturation is the alternative structure adopted by the sequence in vivo. This suggests that negative superhelical stress sufficient for local denaturation exists in nucleosomal DNA. We also demonstrate by micrococcal nuclease digestions that the deletion of the alternating d(TA)n sequence modifies the chromatin hypersensitive site but does not affect nucleosome positioning.

摘要

我们在此探讨酿酒酵母FBP1基因3'区域发现的天然交替d(TA)n序列的体内结构问题。该序列由13个TA对组成,在序列中间被一个TT二核苷酸打断。先前使用十字形特异性核酸酶S1和核酸内切酶VII进行的实验证明,该区域在体外存在十字形结构。我们还表明,该区域是酵母染色质中一个对核酸酶敏感的位点的一部分,两侧是核小体。在此,我们通过体内S1足迹法证明,在酵母质粒中该序列在体内也采用非B-DNA结构,且不是十字形结构。对该区域的理论分析表明,它包含一个易受超螺旋应力影响的双链解链位点。野生型序列和缺失突变体中形成替代结构的位置和条件与这些理论预测一致,表明某种变性是该序列在体内采用的替代结构。这表明核小体DNA中存在足以导致局部变性的负超螺旋应力。我们还通过微球菌核酸酶消化证明,交替d(TA)n序列的缺失改变了染色质超敏位点,但不影响核小体定位。

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