Structural Basis for the Versatile and Methylation-Dependent Binding of CTCF to DNA

被引:183
作者
Hashimoto, Hideharu [1 ]
Wang, Dongxue [1 ]
Horton, John R. [1 ,2 ]
Zhang, Xing [1 ,2 ]
Corces, Victor G. [3 ]
Cheng, Xiaodong [1 ,2 ]
机构
[1] Emory Univ, Sch Med, Dept Biochem, 1510 Clifton Rd NE, Atlanta, GA 30322 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Houston, TX 77030 USA
[3] Emory Univ, Dept Biol, 1510 Clifton Rd NE, Atlanta, GA 30322 USA
关键词
ZINC FINGERS; CRYSTAL-STRUCTURE; CPG METHYLATION; RECOGNITION; GENOME; COMPLEX; SITES; CHROMATIN; INSULATION; MAP;
D O I
10.1016/j.molcel.2017.05.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The multidomain CCCTC-binding factor (CTCF), containing a tandem array of 11 zinc fingers (ZFs), modulates the three-dimensional organization of chromatin. We crystallized the human CTCF DNA-binding domain in complex with a known CTCF-binding site. While ZF2 does not make sequence-specific contacts, each finger of ZF3-7 contacts three bases of the 15-bp consensus sequence. Each conserved nucleotide makes base-specific hydrogen bonds with a particular residue. Most of the variable base pairs within the core sequence also engage in interactions with the protein. These interactions compensate for deviations from the consensus sequence, allowing CTCF to adapt to sequence variations. CTCF is sensitive to cytosine methylation at position 2, but insensitive at position 12 of the 15-bp core sequence. These differences can be rationalized structurally. Although included in crystallizations, ZF10 and ZF11 are not visible, while ZF8 and ZF9 span the backbone of the DNA duplex, conferring no sequence specificity but adding to overall binding stability.
引用
收藏
页码:711 / +
页数:13
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