2KYP
Monomeric Human CKIT-2 proto-oncogene promoter quadruplex DNA NMR, 12 structures
2KYP の概要
| エントリーDOI | 10.2210/pdb2kyp/pdb |
| 関連するPDBエントリー | 2kyo |
| 分子名称 | 5'-D(*CP*GP*GP*GP*CP*GP*GP*GP*CP*GP*CP*TP*AP*GP*GP*GP*AP*GP*GP*GP*T)-3' (1 entity in total) |
| 機能のキーワード | g-tetrad, all-parallel quadruplex, intergenic recombination, dna |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 6626.25 |
| 構造登録者 | |
| 主引用文献 | Kuryavyi, V.,Phan, A.T.,Patel, D.J. Solution structures of all parallel-stranded monomeric and dimeric G-quadruplex scaffolds of the human c-kit2 promoter. Nucleic Acids Res., 38:6757-6773, 2010 Cited by PubMed Abstract: Previous studies have demonstrated that nuclease hypersensitivity regions of several proto-oncogenic DNA promoters, situated upstream of transcription start sites, contain guanine-rich tracts that form intramolecular G-quadruplexes stabilized by stacked G•G•G•G tetrads in monovalent cation solution. The human c-kit oncogenic promoter, an important target in the treatment of gastrointestinal tumors, contains two such stretches of guanine-rich tracts, designated c-kit1 and c-kit2. Our previous nuclear magnetic resonance (NMR)-based studies reported on the novel G-quadruplex scaffold of the c-kit1 promoter in K(+)-containing solution, where we showed for the first time that even an isolated guanine was involved in G-tetrad formation. These NMR-based studies are now extended to the c-kit2 promoter, which adopts two distinct all-parallel-stranded conformations in slow exchange, one of which forms a monomeric G-quadruplex (form-I) in 20 mM K(+)-containing solution and the other a novel dimeric G-quadruplex (form-II) in 100 mM K(+)-containing solution. The c-kit2 promoter dimeric form-II G-quadruplex adopts an unprecedented all-parallel-stranded topology where individual c-kit2 promoter strands span a pair of three-G-tetrad-layer-containing all-parallel-stranded G-quadruplexes aligned in a 3' to 5'-end orientation, with stacking continuity between G-quadruplexes mediated by a sandwiched A•A non-canonical pair. We propose that strand exchange during recombination events within guanine-rich segments, could potentially be mediated by a synapsis intermediate involving an intergenic parallel-stranded dimeric G-quadruplex. PubMed: 20566478DOI: 10.1093/nar/gkq558 主引用文献が同じPDBエントリー |
| 実験手法 | SOLUTION NMR |
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