Enzymatic properties of recombinant Dnmt3a DNA methyltransferase from mouse: the enzyme modifies DNA in a non-processive manner and also methylates non-CpG [correction of non-CpA] sites
- PMID: 11399089
- DOI: 10.1006/jmbi.2001.4710
Enzymatic properties of recombinant Dnmt3a DNA methyltransferase from mouse: the enzyme modifies DNA in a non-processive manner and also methylates non-CpG [correction of non-CpA] sites
Erratum in
- J Mol Biol 2001 Jul 20;310(4):951
Abstract
We present the first in vitro study investigating the catalytic properties of a mammalian de novo DNA methyltransferase. Dnmt3a from mouse was cloned and expressed in Escherichia coli. It was shown to be catalytically active in E. coli cells in vivo. The methylation activity of the purified protein was highest at pH 7.0 and 30 mM KCl. Our data show that recombinant Dnmt3a protein is indeed a de novo methyltransferase, as it catalyzes the transfer of methyl groups to unmethylated substrates with similar efficiency as to hemimethylated substrates. With oligonucleotide substrates, the catalytic activity of Dnmt3a is similar to that of Dnmt1: the K(m) values for the unmethylated and hemimethylated oligonucleotide substrates are 2.5 microM, and the k(cat) values are 0.05 h(-1) and 0.07 h(-1), respectively. The enzyme catalyzes the methylation of DNA in a distributive manner, suggesting that Dnmt3a and Dnmt1 may cooperate during de novo methylation of DNA. Further, we investigated the methylation activity of Dnmt3a at non-canonical sites. Even though the enzyme shows maximum activity at CpG sites, with oligonucleotide substrates, a high methylation activity was also found at CpA sites, which are modified only twofold slower than CpG sites. Therefore, the specificity of Dnmt3a is completely different from that of the maintenance methyltransferase Dnmt1, which shows a 40 to 50-fold preference for hemimethylated over unmethylated CpG sites and has almost no methylation activity at non-CpG sites.
Copyright 2001 Academic Press.
Similar articles
-
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 Mol Biol. 2001 Jun 22;309(5):1189-99. doi: 10.1006/jmbi.2001.4709. J Mol Biol. 2001. PMID: 11399088
-
Murine DNA cytosine-C5 methyltransferase: pre-steady- and steady-state kinetic analysis with regulatory DNA sequences.Biochemistry. 1996 Jun 11;35(23):7308-15. doi: 10.1021/bi9600512. Biochemistry. 1996. PMID: 8652507
-
De novo CpG island methylation in human cancer cells.Cancer Res. 2006 Jan 15;66(2):682-92. doi: 10.1158/0008-5472.CAN-05-1980. Cancer Res. 2006. PMID: 16423997
-
Regulation of expression and activity of DNA (cytosine-5) methyltransferases in mammalian cells.Prog Mol Biol Transl Sci. 2011;101:311-33. doi: 10.1016/B978-0-12-387685-0.00009-3. Prog Mol Biol Transl Sci. 2011. PMID: 21507356 Review.
-
Structure and function of mammalian DNA methyltransferases.Chembiochem. 2011 Jan 24;12(2):206-22. doi: 10.1002/cbic.201000195. Epub 2010 Nov 29. Chembiochem. 2011. PMID: 21243710 Review.
Cited by
-
Distribution, recognition and regulation of non-CpG methylation in the adult mammalian brain.Nat Neurosci. 2014 Feb;17(2):215-22. doi: 10.1038/nn.3607. Epub 2013 Dec 22. Nat Neurosci. 2014. PMID: 24362762 Free PMC article.
-
Distinctive Klf4 mutants determine preference for DNA methylation status.Nucleic Acids Res. 2016 Dec 1;44(21):10177-10185. doi: 10.1093/nar/gkw774. Epub 2016 Sep 4. Nucleic Acids Res. 2016. PMID: 27596594 Free PMC article.
-
Complex DNA sequence readout mechanisms of the DNMT3B DNA methyltransferase.Nucleic Acids Res. 2020 Nov 18;48(20):11495-11509. doi: 10.1093/nar/gkaa938. Nucleic Acids Res. 2020. PMID: 33105482 Free PMC article.
-
DNA methylation and demethylation in mammals.J Biol Chem. 2011 May 27;286(21):18347-53. doi: 10.1074/jbc.R110.205286. Epub 2011 Mar 24. J Biol Chem. 2011. PMID: 21454628 Free PMC article. Review.
-
Epigenetics: New Insights into Mammary Gland Biology.Genes (Basel). 2021 Feb 5;12(2):231. doi: 10.3390/genes12020231. Genes (Basel). 2021. PMID: 33562534 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Miscellaneous