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Iterative Optimization of DNA Duplexes for Crystallization of SeqA-DNA Complexes
Published on: November 1, 2012
Bending of DNA duplexes with mutation motifs
Michal Růžička1,2, Přemysl Souček1, Petr Kulhánek1,3
1CEITEC - Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
Abstract:
Mutations can be induced by environmental factors but also arise spontaneously during DNA replication or due to deamination of methylated cytosines at CpG dinucleotides. Sites where mutations occur with higher frequency than would be expected by chance are termed hotspots while sites that contain mutations rarely are termed coldspots. Mutations are permanently scanned and repaired by repair systems. Among them, the mismatch repair targets base pair mismatches, which are discriminated from canonical base pairs by probing altered elasticity of DNA. Using biased molecular dynamics simulations, we investigated the elasticity of coldspots and hotspots motifs detected in human genes associated with inherited disorders, and also of motifs with Czech population hotspots and de novo mutations. Main attention was paid to mutations leading to G/T and A+/C pairs. We observed that hotspots without CpG/CpHpG sequences are less flexible than coldspots, which indicates that flexible sequences are more effectively repaired. In contrary, hotspots with CpG/CpHpG sequences exhibited increased flexibility as coldspots. Their mutability is more likely related to spontaneous deamination of methylated cytosines leading to C > T mutations, which are primarily targeted by base excision repair. We corroborated conclusions based on computer simulations by measuring melting curves of hotspots and coldspots containing G/T mismatch.
Insights
DNA mutation hotspots are less flexible than coldspots, suggesting better repair of flexible sequences. However, CpG-containing hotspots show increased flexibility, linked to deamination and repair by base excision repair systems.
Area of Science:
- Molecular Biology
- Genetics
- Biophysics
Background:
- Mutations arise spontaneously or from environmental factors, with hotspots and coldspots exhibiting differential mutation frequencies.
- DNA repair systems, including mismatch repair, constantly scan and fix DNA alterations.
- Altered DNA elasticity is a key factor in discriminating mismatched base pairs.
Purpose of the Study:
- Investigate the elasticity of DNA coldspots and hotspots associated with inherited disorders and de novo mutations.
- Analyze the mechanical properties of G/T and A+/C mutation sites.
- Correlate DNA elasticity with mutation frequency and repair mechanisms.
Main Methods:
- Biased molecular dynamics simulations to assess DNA elasticity.
- Analysis of mutation hotspots and coldspots in human genes.
- Melting curve analysis of G/T mismatch-containing sequences.
Main Results:
- Non-CpG/CpHpG hotspots were less flexible than coldspots, indicating efficient repair of flexible sequences.
- CpG/CpHpG hotspots displayed increased flexibility, similar to coldspots.
- Increased flexibility in CpG hotspots suggests mutability is linked to methylated cytosine deamination and base excision repair.
Conclusions:
- DNA sequence flexibility influences mutation repair efficiency.
- CpG dinucleotides within hotspots contribute to increased flexibility and specific mutation pathways (C > T).
- Molecular dynamics simulations and experimental melting curves provide insights into mutation mechanisms.
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