2KKF

Solution structure of MLL CXXC domain in complex with palindromic CPG DNA

2KKF の概要

• エントリーDOI: 10.2210/pdb2kkf/pdb
• 分子名称: Histone-lysine N-methyltransferase HRX, 5'-D(*CP*CP*CP*TP*GP*CP*GP*CP*AP*GP*GP*G)-3', ZINC ION (3 entities in total)
• 機能のキーワード: protein-dna complex, cxxc domain, mll, cpg dna, chromosomal rearrangement, dna-binding, metal-binding, nucleus, zinc-finger, dna binding protein-dna complex, alternative splicing, apoptosis, bromodomain, chromatin regulator, isopeptide bond, methyltransferase, phosphoprotein, polymorphism, proto-oncogene, s-adenosyl-l-methionine, transcription, transcription regulation, transferase, ubl conjugation, zinc, dna binding protein/dna
• 由来する生物種: Homo sapiens (human); 詳細
• 細胞内の位置: Nucleus. MLL cleavage product N320: Nucleus. MLL cleavage product C180: Nucleus: Q03164
• タンパク質・核酸の鎖数: 3
• 化学式量合計: 14137.57

構造登録者

Cierpicki, T.,Riesbeck, J.E.,Grembecka, J.E.,Lukasik, S.M.,Popovic, R.,Omonkowska, M.,Shultis, D.S.,Zeleznik-Le, N.J.,Bushweller, J.H. (登録日: 2009-06-18, 公開日: 2009-12-08, 最終更新日: 2024-05-22)

主引用文献

Cierpicki, T.,Risner, L.E.,Grembecka, J.,Lukasik, S.M.,Popovic, R.,Omonkowska, M.,Shultis, D.D.,Zeleznik-Le, N.J.,Bushweller, J.H.
Structure of the MLL CXXC domain-DNA complex and its functional role in MLL-AF9 leukemia.
Nat.Struct.Mol.Biol., 17:62-68, 2010

PubMed Abstract: The gene MLL (encoding the protein mixed-lineage leukemia) is the target of chromosomal translocations that cause leukemias with poor prognosis. All leukemogenic MLL fusion proteins retain the CXXC domain, which binds to nonmethylated CpG DNA sites. We present the solution structure of the MLL CXXC domain in complex with DNA, showing how the CXXC domain distinguishes nonmethylated from methylated CpG DNA. On the basis of the structure, we generated point mutations that disrupt DNA binding. Introduction of these mutations into the MLL-AF9 fusion protein resulted in increased DNA methylation of specific CpG nucleotides in Hoxa9, increased H3K9 methylation, decreased expression of Hoxa9-locus transcripts, loss of immortalization potential, and inability to induce leukemia in mice. These results establish that DNA binding by the CXXC domain and protection against DNA methylation is essential for MLL fusion leukemia. They also provide support for viewing this interaction as a potential target for therapeutic intervention.

PubMed: 20010842
DOI: 10.1038/nsmb.1714

実験手法

SOLUTION NMR