Formation of Sequence-Independent Z-DNA Induced by a Ruthenium Complex at Low Salt Concentrations
Formation of Sequence-Independent Z-DNA Induced by a Ruthenium Complex at Low Salt Concentrations
复制标题
低盐浓度下钌络合物诱导形成与序列无关的 Z-DNA
DOI:
10.1002/anie.201104422
复制
发表时间:
2011-01-01
影响因子:
16.6
通讯作者:
Zhou, Xiang
中科院分区:
文献类型:
--
作者:
Wu, Zhiguo;Tian, Tian;Zhou, Xiang
Z-DNA has attracted much attention during the past 30 years.[1] The high binding affinity of some proteins to ZDNA [2–4] means that these sequences are novel and important regulators of several genes, such as C-MYC, CSF1, and human ADAM-12.[5–7] Liu et al. reported the distribution of Z-DNA sequences and their effects on transcription.[8] It is generally agreed that potential Z-DNA-forming sequences are located near the promoter region of most human genes, and that Z-DNAs upregulate transcription.[9, 10] In addition, ZDNA may affect chromatin recombination and nucleosome positioning.[11]Various sequences of natural polynucleotides, especially non-alternating pyrimidine–purine (non-APP) or AT-rich sequences, are rarely found in the Z-DNA conformation. Instead, this conformation is favored by alternating GC sequences, which usually contain alternating syn-G and anti-C nucleosides.[12] AT base pairs that are inserted into Z-DNA sequences destabilize the conformation and induce a DNA cruciform.[13, 14] Non-APP segments, especially AnTn (n> 2), cause the DNA to bend into so-called adenine–thymine tracts (AT tracts), which prevent the formation of Z-DNA.[15, 16] To date, the number of reported sequences that adopt the ZDNA conformation is limited, and most of these sequences are GC-rich. In fact, GC-rich Z-DNA usually occurs at extremely high salt concentrations or at a considerable concentration of multivalent cations, such as Ca2+, Mg2+,