Mechanistic Details of the DNA Recognition by the Dnmt1 DNA Methyltransferase
Overview
Affiliations
A recently solved Dnmt1-DNA crystal structure revealed several enzyme-DNA contacts and large structural rearrangements of the DNA at the target site, including the flipping of the non-target strand base of the base pair flanking the CpG site and formation of a non-canonical base pair between the non-target strand Gua and the flanking base pair. Here, we show that the contacts of the enzyme to the target base and the Gua:5mC base pair that are observed in the structure are very important for catalytic activity. The contacts to the non-target strand Gua are not important since its exchange by Ade stimulated activity. Except target base flipping, we could not find evidence that the DNA rearrangements have a functional role.
Cytosine analogues as DNA methyltransferase substrates.
Wojciechowski M, Czapinska H, Krwawicz J, Rafalski D, Bochtler M Nucleic Acids Res. 2024; 52(15):9267-9281.
PMID: 38966999 PMC: 11347137. DOI: 10.1093/nar/gkae568.
Enzymology of Mammalian DNA Methyltransferases.
Jurkowska R, Jeltsch A Adv Exp Med Biol. 2022; 1389:69-110.
PMID: 36350507 DOI: 10.1007/978-3-031-11454-0_4.
Adam S, Anteneh H, Hornisch M, Wagner V, Lu J, Radde N Nat Commun. 2020; 11(1):3723.
PMID: 32709850 PMC: 7381644. DOI: 10.1038/s41467-020-17531-8.
Ming X, Zhang Z, Zou Z, Lv C, Dong Q, He Q Cell Res. 2020; 30(11):980-996.
PMID: 32581343 PMC: 7785024. DOI: 10.1038/s41422-020-0359-9.
Dumesic P, Stoddard C, Catania S, Narlikar G, Madhani H Mol Cell. 2020; 79(1):127-139.e4.
PMID: 32437639 PMC: 7335330. DOI: 10.1016/j.molcel.2020.04.029.