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
相关论文
共 23 条
[1]   Solution structure of the nonmethyl-CpG-binding CXXC domain of the leukaemia-associated MLL histone methyltransferase [J].
Allen, Mark D. ;
Grummitt, Charles G. ;
Hilcenko, Christine ;
Min, Sandra Young ;
Tonkin, Louise M. ;
Johnson, Christopher M. ;
Freund, Stefan M. ;
Bycroft, Mark ;
Warren, Alan J. .
EMBO JOURNAL, 2006, 25 (19) :4503-4512
[2]   The DNMT1 target recognition domain resides in the N terminus [J].
Araujo, FD ;
Croteau, S ;
Slack, AD ;
Milutinovic, S ;
Bigey, P ;
Price, GB ;
Zannis-Hajopoulos, M ;
Szyf, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (10) :6930-6936
[3]   Binding to nonmethylated CpG DNA is essential for target recognition, transactivation, and myeloid transformation by an MLL oncoprotein [J].
Ayton, PM ;
Chen, EH ;
Cleary, ML .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (23) :10470-10478
[4]   The activity of the murine DNA methyltransferase Dnmt1 is controlled by interaction of the catalytic domain with the N-terminal part of the enzyme leading to an allosteric activation of the enzyme after binding to methylated DNA [J].
Fatemi, M ;
Hermann, A ;
Pradhan, S ;
Jeltsch, A .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 309 (05) :1189-1199
[5]   Epigenetic Reprogramming in Plant and Animal Development [J].
Feng, Suhua ;
Jacobsen, Steven E. ;
Reik, Wolf .
SCIENCE, 2010, 330 (6004) :622-627
[6]   Different Binding Properties and Function of CXXC Zinc Finger Domains in Dnmt1 and Tet1 [J].
Frauer, Carina ;
Rottach, Andrea ;
Meilinger, Daniela ;
Bultmann, Sebastian ;
Fellinger, Karin ;
Hasenoeder, Stefan ;
Wang, Mengxi ;
Qin, Weihua ;
Soeding, Johannes ;
Spada, Fabio ;
Leonhardt, Heinrich .
PLOS ONE, 2011, 6 (02)
[7]   Molecular enzymology of the catalytic domains of the Dnmt3a and Dnmt3b DNA methyltransferases [J].
Gowher, H ;
Jeltsch, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) :20409-20414
[8]   Accuracy of DNA methylation pattern preservation by the Dnmt1 methyltransferase [J].
Goyal, R ;
Reinhardt, R ;
Jeltsch, A .
NUCLEIC ACIDS RESEARCH, 2006, 34 (04) :1182-1188
[9]   The Dnmt1 DNA-(cytosine-C5)-methyltransferase methylates DNA processively with high preference for hemimethylated target sites [J].
Hermann, A ;
Goyal, R ;
Jeltsch, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (46) :48350-48359
[10]   Structure and substrate recognition of the Escherichia coli DNA adenine methyltransferase [J].
Horton, JR ;
Liebert, K ;
Bekes, M ;
Jeltsch, A ;
Cheng, XD .
JOURNAL OF MOLECULAR BIOLOGY, 2006, 358 (02) :559-570