Human DNMT1 transition state structure

Proc Natl Acad Sci U S A. 2016 Mar 15;113(11):2916-21. doi: 10.1073/pnas.1522491113. Epub 2016 Feb 29.

Abstract

Human DNA methyltransferase 1 (DNMT1) maintains the epigenetic state of DNA by replicating CpG methylation signatures from parent to daughter strands, producing heritable methylation patterns through cell divisions. The proposed catalytic mechanism of DNMT1 involves nucleophilic attack of Cys(1226) to cytosine (Cyt) C6, methyl transfer from S-adenosyl-l-methionine (SAM) to Cyt C5, and proton abstraction from C5 to form methylated CpG in DNA. Here, we report the subangstrom geometric and electrostatic structure of the major transition state (TS) of the reaction catalyzed by human DNMT1. Experimental kinetic isotope effects were used to guide quantum mechanical calculations to solve the TS structure. Methyl transfer occurs after Cys(1226) attack to Cyt C6, and the methyl transfer step is chemically rate-limiting for DNMT1. Electrostatic potential maps were compared for the TS and ground states, providing the electronic basis for interactions between the protein and reactants at the TS. Understanding the TS of DNMT1 demonstrates the possibility of using similar analysis to gain subangstrom geometric insight into the complex reactions of epigenetic modifications.

Keywords: 5-methylcytosine; CpG methylation; DNA methyltransferase; S-adenosyl-l-methionine; transition state.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding, Competitive
  • Carbon Isotopes / chemistry
  • Carbon Radioisotopes / chemistry
  • Catalysis
  • Cysteine / chemistry
  • Cytosine / chemistry
  • Cytosine / metabolism
  • DNA (Cytosine-5-)-Methyltransferase 1
  • DNA (Cytosine-5-)-Methyltransferases / chemistry*
  • DNA (Cytosine-5-)-Methyltransferases / metabolism
  • DNA Methylation
  • Deuterium / chemistry
  • Humans
  • Kinetics
  • Models, Molecular
  • Protein Structure, Tertiary
  • Recombinant Fusion Proteins / chemistry
  • Recombinant Fusion Proteins / metabolism
  • S-Adenosylhomocysteine / metabolism
  • Tritium / chemistry

Substances

  • Carbon Isotopes
  • Carbon Radioisotopes
  • Recombinant Fusion Proteins
  • Tritium
  • Cytosine
  • S-Adenosylhomocysteine
  • Deuterium
  • DNA (Cytosine-5-)-Methyltransferase 1
  • DNA (Cytosine-5-)-Methyltransferases
  • DNMT1 protein, human
  • Cysteine