Specificity of Dnmt1 for Methylation of Hemimethylated CpG Sites Resides in Its Catalytic Domain

被引:67
作者
Bashtrykov, Pavel [1 ,2 ]
Jankevicius, Gytis [3 ]
Smarandache, Anita [4 ]
Jurkowska, Renata Z. [1 ,2 ]
Ragozin, Sergey [1 ,2 ]
Jeltsch, Albert [1 ,2 ]
机构
[1] Univ Stuttgart, Inst Biochem, Fac Chem, D-70569 Stuttgart, Germany
[2] Jacobs Univ Bremen, Sch Engn & Sci, D-28759 Bremen, Germany
[3] Jacobs Univ Bremen, Mol Life Sci Program, D-28759 Bremen, Germany
[4] Jacobs Univ Bremen, Biochem & Cell Biol Program, D-28759 Bremen, Germany
来源
CHEMISTRY & BIOLOGY | 2012年 / 19卷 / 05期
关键词
MAINTENANCE DNA METHYLATION; TARGET RECOGNITION; CXXC DOMAIN; METHYLTRANSFERASE; BINDING; COMPLEX; ENZYME;
D O I
10.1016/j.chembiol.2012.03.010
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 maintenance methylation of hemimethylated CpG sites by the DNA methyltransferase Dnmt1 is the molecular basis of the inheritance of DNA methylation patterns. Based on structural data and kinetics obtained with a truncated form of Dnmt1, an autoinhibition model for the specificity of Dnmt1 was proposed in which unmethylated DNA binds to Dnmt1's CXXC domain, which prevents its methylation. We have prepared CXXC domain variants that lost DNA binding. Corresponding full-length Dnmt1 variants did not display a reduction in specificity, indicating that the autoinhibition model does not apply in full-length Dnmt1. Furthermore, we show that the Dnmt1 M1235S variant, which carries an exchange in the catalytic domain of the enzyme, has a marked reduction in specificity, indicating that the recognition of the hemimethylated state of target sites resides within the catalytic domain.
引用
收藏
页码:572 / 578
页数:7
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