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Published on: March 5, 2018
Forming a chromium-based interstrand DNA crosslink: Implications for carcinogenicity.
Silas Brown1, Sydney Marchi1, C Sumner Thomas1
1Department of Chemistry and Biochemistry, The University of Alabama, Tuscaloosa, AL 35487-0336, USA.
Chromate reduction forms DNA lesions. Researchers elucidated a binuclear chromium(III) assembly bridging DNA strands, suggesting chromate-induced interstrand crosslinks may be organic, not inorganic.
Area of Science:
- Environmental Science
- Biochemistry
- Toxicology
Background:
- Chromate reduction generates Cr(III)-DNA lesions, including binary adducts, interstrand crosslinks, and ternary adducts.
- While binary adduct structures are known, interstrand crosslink and ternary adduct structures remain uncharacterized.
- Understanding these structures is crucial for assessing chromate's genotoxicity.
Purpose of the Study:
- To elucidate the structure of Cr(III)-mediated DNA interstrand crosslinks.
- To investigate the binding of Cr(III) to a specific oligonucleotide sequence (5'-CG site).
Main Methods:
- Analysis of Chromium(III) binding to a synthetic oligonucleotide duplex containing a 5'-CG site.
- Structural elucidation of the resulting Cr(III)-DNA complex.
Main Results:
- A novel oxide- or hydroxide-bridged binuclear Cr(III) assembly bridging two DNA strands was identified.
- One Cr(III) ion coordinated to the N-7 atom of a guanine residue.
- The complex formed a hydrogen bond between another guanine and a Cr(III)-bound aquo ligand, without involving the phosphate backbone.
Conclusions:
- The identified Cr-O(H)-Cr bridged complex structure differs significantly from previously reported Cr-induced interstrand crosslinks.
- This suggests that Cr-induced interstrand crosslinks resulting from chromate reduction may possess an organic structure.
- Further research is needed to fully characterize the diverse mechanisms of chromate-DNA interaction.
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