人ADAR1的Zα结构域与CG重复DNA双链优先结合的NMR研究

IF 0.4 Q4 BIOCHEMICAL RESEARCH METHODS
Ae-Ree Lee, Seo-Ree Choi, Yeo-Jin Seo, Joon-Hwa Lee
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引用次数: 0

摘要

人类ADAR1的Z-DNA结构域(ZαADAR1)通过优先结合CG重复片段和破坏邻近富含AT的区域的稳定来产生B-Z连接DNA。9然而,这项研究无法回答富含AT的区域中有多少碱基对因ZαADAR1的结合而不稳定的问题。因此,我们对含有8碱基对(8-bp)CG重复片段和12bp AT富集区的较长DNA双链体进行了ZαADAR1的NMR实验。这项研究表明,在长DNA中,ZαADAR1优先与CG重复片段结合,而不是与富含AT的区域结合,然后使相邻富含AT区域中的至少6个碱基对不稳定,以实现CG重复片段的有效B-Z过渡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NMR Study on the Preferential Binding of the Zα Domain of Human ADAR1 to CG-repeat DNA Duplex
The Z-DNA domain of human ADAR1 (Zα ADAR1 ) produces B-Z junction DNA through preferential binding to the CG-repeat segment and destabilizing the neighboring AT-rich region. 9 However, this study could not answer the question of how many base-pairs in AT-rich region are destabilized by binding of Zα ADAR1 . Thus, we have performed NMR experiments of Zα ADAR1 to the longer DNA duplex containing an 8-base-paired (8-bp) CG-repeat segment and a 12-bp AT-rich region. This study revealed that Zα ADAR1 preferentially binds to the CG-repeat segment rather than AT-rich region in a long DNA and then destabilizes at least 6 base-pairs in the neighboring AT-rich region for efficient B-Z transition of the CG-repeat segment.
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来源期刊
Journal of the Korean magnetic resonance society
Journal of the Korean magnetic resonance society BIOCHEMICAL RESEARCH METHODS-
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