Structure-specific binding of MeCP2 to four-way junction DNA through its methyl CpG-binding domain

TC Galvao, JO Thomas - Nucleic acids research, 2005 - academic.oup.com
TC Galvao, JO Thomas
Nucleic acids research, 2005academic.oup.com
MeCP2, whose methylated DNA-binding domain (MBD) binds preferentially to DNA
containing 5Me-CpG relative to linear unmethylated DNA, also binds preferentially, and with
similar affinity, to unmethylated four-way DNA junctions through the MBD. The Arg133Cys
(R133C) mutation in the MBD, a Rett syndrome mutation that abolishes binding to
methylated DNA, leads to only a slight reduction in the affinity of the MBD for four-way
junctions, suggesting distinct but partially overlapping modes of binding to junction and …
Abstract
MeCP2, whose methylated DNA-binding domain (MBD) binds preferentially to DNA containing 5Me-CpG relative to linear unmethylated DNA, also binds preferentially, and with similar affinity, to unmethylated four-way DNA junctions through the MBD. The Arg133Cys (R133C) mutation in the MBD, a Rett syndrome mutation that abolishes binding to methylated DNA, leads to only a slight reduction in the affinity of the MBD for four-way junctions, suggesting distinct but partially overlapping modes of binding to junction and methylated DNA. Binding to unmethylated DNA junctions is likely to involve a subset of the interactions that occur with methylated DNA. High-affinity, methylation-independent binding to four-way junctions is consistent with additional roles for MeCP2 in chromatin, beyond recognition of 5Me-CpG.
Oxford University Press