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Updated: May 31, 2026

In Vitro Directed Evolution of a Restriction Endonuclease with More Stringent Specificity
Published on: March 25, 2020
The MspJI family of modification-dependent restriction endonucleases for epigenetic studies
Devora Cohen-Karni1, Derrick Xu, Lynne Apone
1Molecular Biology, Cell Biology, and Biochemistry Program, Boston University, Boston, MA 02215, USA.
Abstract:
MspJI is a novel modification-dependent restriction endonuclease that cleaves at a fixed distance away from the modification site. Here, we present the biochemical characterization of several MspJI homologs, including FspEI, LpnPI, AspBHI, RlaI, and SgrTI. All of the enzymes specifically recognize cytosine C5 modification (methylation or hydroxymethylation) in DNA and cleave at a constant distance (N(12)/N(16)) away from the modified cytosine. Each displays its own sequence context preference, favoring different nucleotides flanking the modified cytosine. By cleaving on both sides of fully modified CpG sites, they allow the extraction of 32-base long fragments around the modified sites from the genomic DNA. These enzymes provide powerful tools for direct interrogation of the epigenome. For example, we show that RlaI, an enzyme that prefers (m)CWG but not (m)CpG sites, generates digestion patterns that differ between plant and mammalian genomic DNA, highlighting the difference between their epigenomic patterns. In addition, we demonstrate that deep sequencing of the digested DNA fragments generated from these enzymes provides a feasible method to map the modified sites in the genome. Altogether, the MspJI family of enzymes represent appealing tools of choice for method development in DNA epigenetic studies.
Insights
MspJI enzymes recognize DNA modifications and cut DNA at a fixed distance, enabling epigenome analysis. These novel tools facilitate mapping modified sites for DNA epigenetic studies.
Area of Science:
- Molecular Biology
- Epigenetics
- Biochemistry
Background:
- MspJI is a restriction enzyme that cleaves DNA based on modification status.
- Understanding DNA modifications is crucial for epigenomic research.
Purpose of the Study:
- To biochemically characterize MspJI homologs.
- To evaluate their utility in epigenome analysis and mapping modified DNA sites.
Main Methods:
- Biochemical characterization of MspJI homologs (FspEI, LpnPI, AspBHI, RlaI, SgrTI).
- DNA cleavage assays at specific distances from cytosine C5 modifications.
- Deep sequencing of digested DNA fragments.
Main Results:
- All characterized enzymes recognize cytosine C5 modifications (methylation/hydroxymethylation).
- Enzymes cleave DNA at a constant distance (N12/N16) from modified cytosines with sequence context preferences.
- Cleavage around CpG sites allows extraction of 32-base fragments for epigenome interrogation.
- RlaI distinguishes plant and mammalian DNA epigenomic patterns.
- Deep sequencing enables genome-wide mapping of modified DNA sites.
Conclusions:
- The MspJI family of enzymes are valuable tools for DNA epigenetics.
- These enzymes facilitate direct interrogation and mapping of the epigenome.
- They offer novel methods for DNA epigenetic studies and research.
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