Back to Search
Start Over
Caulobacter crescentus Cell Cycle-Regulated DNA Methyltransferase Uses a Novel Mechanism for Substrate Recognition.
- Source :
-
Biochemistry [Biochemistry] 2017 Aug 01; Vol. 56 (30), pp. 3913-3922. Date of Electronic Publication: 2017 Jul 18. - Publication Year :
- 2017
-
Abstract
- Caulobacter crescentus relies on DNA methylation by the cell cycle-regulated methyltransferase (CcrM) in addition to key transcription factors to control the cell cycle and direct cellular differentiation. CcrM is shown here to efficiently methylate its cognate recognition site 5'-GANTC-3' in single-stranded and hemimethylated double-stranded DNA. We report the K <subscript>m</subscript> , k <subscript>cat</subscript> , k <subscript>methylation</subscript> , and K <subscript>d</subscript> for single-stranded and hemimethylated substrates, revealing discrimination of 10 <superscript>7</superscript> -fold for noncognate sequences. The enzyme also shows a similar discrimination against single-stranded RNA. Two independent assays clearly show that CcrM is highly processive with single-stranded and hemimethylated DNA. Collectively, the data provide evidence that CcrM and other DNA-modifying enzymes may use a new mechanism to recognize DNA in a key epigenetic process.
- Subjects :
- Caulobacter crescentus cytology
Cell Cycle
Coenzymes metabolism
DNA chemistry
DNA, Single-Stranded chemistry
Electrophoretic Mobility Shift Assay
Fluoresceins analysis
Fluorescent Dyes analysis
Kinetics
Nucleotide Motifs
RNA chemistry
RNA metabolism
Recombinant Fusion Proteins metabolism
Recombinant Proteins metabolism
S-Adenosylmethionine metabolism
Site-Specific DNA-Methyltransferase (Adenine-Specific) genetics
Substrate Specificity
Thermodynamics
Tritium
Caulobacter crescentus enzymology
DNA metabolism
DNA Methylation
DNA, Single-Stranded metabolism
Site-Specific DNA-Methyltransferase (Adenine-Specific) metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4995
- Volume :
- 56
- Issue :
- 30
- Database :
- MEDLINE
- Journal :
- Biochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 28661661
- Full Text :
- https://doi.org/10.1021/acs.biochem.7b00378