6C1V
MBD2 in complex with double-stranded DNA
6C1V の概要
エントリーDOI | 10.2210/pdb6c1v/pdb |
分子名称 | Methyl-CpG-binding domain protein 2, 12-mer DNA, UNKNOWN ATOM OR ION, ... (5 entities in total) |
機能のキーワード | mbd, dna-binding, structural genomics, structural genomics consortium, sgc, dna binding protein-dna complex, dna binding protein/dna |
由来する生物種 | Homo sapiens (Human) 詳細 |
細胞内の位置 | Nucleus : Q9UBB5 |
タンパク質・核酸の鎖数 | 8 |
化学式量合計 | 327089.17 |
構造登録者 | Lei, M.,Tempel, W.,Arrowsmith, C.H.,Bountra, C.,Edwards, A.M.,Min, J.,Structural Genomics Consortium (SGC) (登録日: 2018-01-05, 公開日: 2018-02-14, 最終更新日: 2024-04-03) |
主引用文献 | Liu, K.,Xu, C.,Lei, M.,Yang, A.,Loppnau, P.,Hughes, T.R.,Min, J. Structural basis for the ability of MBD domains to bind methyl-CG and TG sites in DNA. J. Biol. Chem., 293:7344-7354, 2018 Cited by PubMed Abstract: Cytosine methylation is a well-characterized epigenetic mark and occurs at both CG and non-CG sites in DNA. Both methylated CG (mCG)- and mCH (H = A, C, or T)-containing DNAs, especially mCAC-containing DNAs, are recognized by methyl-CpG-binding protein 2 (MeCP2) to regulate gene expression in neuron development. However, the molecular mechanism involved in the binding of methyl-CpG-binding domain (MBD) of MeCP2 to these different DNA motifs is unclear. Here, we systematically characterized the DNA-binding selectivities of the MBD domains in MeCP2 and MBD1-4 with isothermal titration calorimetry-based binding assays, mutagenesis studies, and X-ray crystallography. We found that the MBD domains of MeCP2 and MBD1-4 bind mCG-containing DNAs independently of the sequence identity outside the mCG dinucleotide. Moreover, some MBD domains bound to both methylated and unmethylated CA dinucleotide-containing DNAs, with a preference for the CAC sequence motif. We also found that the MBD domains bind to mCA or nonmethylated CA DNA by recognizing the complementary TG dinucleotide, which is consistent with an overlooked ligand of MeCP2, the matrix/scaffold attachment regions (MARs/SARs) with a consensus sequence of 5'-GGTGT-3' that was identified in early 1990s. Our results also explain why MeCP2 exhibits similar binding affinity to both mCA- and hmCA-containing dsDNAs. In summary, our results suggest that in addition to mCG sites, unmethylated CA or TG sites also serve as DNA-binding sites for MeCP2 and other MBD-containing proteins. This discovery expands the genome-wide activity of MBD-containing proteins in gene regulation. PubMed: 29567833DOI: 10.1074/jbc.RA118.001785 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.3 Å) |
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