Literature DB >> 16351098

Spectroscopic characterization of interstrand carbinolamine cross-links formed in the 5'-CpG-3' sequence by the acrolein-derived gamma-OH-1,N2-propano-2'-deoxyguanosine DNA adduct.

Young-Jin Cho1, Hye-Young Kim, Hai Huang, Alvira Slutsky, Irina G Minko, Hao Wang, Lubomir V Nechev, Ivan D Kozekov, Albena Kozekova, Pamela Tamura, Jaison Jacob, Markus Voehler, Thomas M Harris, R Stephen Lloyd, Carmelo J Rizzo, Michael P Stone.   

Abstract

The interstrand N2,N2-dG DNA cross-linking chemistry of the acrolein-derived gamma-OH-1,N2-propanodeoxyguanosine (gamma-OH-PdG) adduct in the 5'-CpG-3' sequence was monitored within a dodecamer duplex by NMR spectroscopy, in situ, using a series of site-specific 13C- and 15N-edited experiments. At equilibrium 40% of the DNA was cross-linked, with the carbinolamine form of the cross-link predominating. The cross-link existed in equilibrium with the non-crosslinked N2-(3-oxo-propyl)-dG aldehyde and its geminal diol hydrate. The ratio of aldehyde/diol increased at higher temperatures. The 1,N2-dG cyclic adduct was not detected. Molecular modeling suggested that the carbinolamine linkage should be capable of maintaining Watson-Crick hydrogen bonding at both of the tandem C x G base pairs. In contrast, dehydration of the carbinolamine cross-link to an imine (Schiff base) cross-link, or cyclization of the latter to form a pyrimidopurinone cross-link, was predicted to require disruption of Watson-Crick hydrogen bonding at one or both of the tandem cross-linked C x G base pairs. When the gamma-OH-PdG adduct contained within the 5'-CpG-3' sequence was instead annealed into duplex DNA opposite T, a mixture of the 1,N2-dG cyclic adduct, the aldehyde, and the diol, but no cross-link, was observed. With this mismatched duplex, reaction with the tetrapeptide KWKK formed DNA-peptide cross-links efficiently. When annealed opposite dA, gamma-OH-PdG remained as the 1,N2-dG cyclic adduct although transient epimerization was detected by trapping with the peptide KWKK. The results provide a rationale for the stability of interstrand cross-links formed by acrolein and perhaps other alpha,beta-unsaturated aldehydes. These sequence-specific carbinolamine cross-links are anticipated to interfere with DNA replication and contribute to acrolein-mediated genotoxicity.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16351098      PMCID: PMC2631571          DOI: 10.1021/ja053897e

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  56 in total

1.  Detection of an interchain carbinolamine cross-link formed in a CpG sequence by the acrolein DNA adduct gamma-OH-1,N( 2)-propano-2'-deoxyguanosine.

Authors:  Hye-Young H Kim; Markus Voehler; Thomas M Harris; Michael P Stone
Journal:  J Am Chem Soc       Date:  2002-08-14       Impact factor: 15.419

2.  Kinetic and thermodynamic analysis of the hydrolytic ring-opening of the malondialdehyde-deoxyguanosine adduct, 3-(2'-deoxy-beta-D-erythro-pentofuranosyl)- pyrimido[1,2-alpha]purin-10(3H)-one.

Authors:  James N Riggins; J Scott Daniels; Carol A Rouzer; Lawrence J Marnett
Journal:  J Am Chem Soc       Date:  2004-07-07       Impact factor: 15.419

3.  Genotoxic mechanism for the major acrolein-derived deoxyguanosine adduct in human cells.

Authors:  In-Young Yang; Francis Johnson; Arthur P Grollman; Masaaki Moriya
Journal:  Chem Res Toxicol       Date:  2002-02       Impact factor: 3.739

4.  Mutagenesis by acrolein-derived propanodeoxyguanosine adducts in human cells.

Authors:  In-Young Yang; Grace Chan; Holly Miller; Yanhe Huang; Maria Cecilia Torres; Francis Johnson; Masaaki Moriya
Journal:  Biochemistry       Date:  2002-11-19       Impact factor: 3.162

5.  Site-specific mutagenesis by a propanodeoxyguanosine adduct carried on an M13 genome.

Authors:  P C Burcham; L J Marnett
Journal:  J Biol Chem       Date:  1994-11-18       Impact factor: 5.157

6.  Site-specific synthesis and reactivity of oligonucleotides containing stereochemically defined 1,N2-deoxyguanosine adducts of the lipid peroxidation product trans-4-hydroxynonenal.

Authors:  Hao Wang; Ivan D Kozekov; Thomas M Harris; Carmelo J Rizzo
Journal:  J Am Chem Soc       Date:  2003-05-14       Impact factor: 15.419

7.  Stereoselective tetrapyrido[2,1-a]isoindolone synthesis via carbanionic and radical intermediates: a model study for the Tacaman alkaloid D/E ring fusion.

Authors:  Roger Hunter; Philip Richards
Journal:  Org Biomol Chem       Date:  2003-07-07       Impact factor: 3.876

8.  DNA interchain cross-links formed by acrolein and crotonaldehyde.

Authors:  Ivan D Kozekov; Lubomir V Nechev; M Scott Moseley; Constance M Harris; Carmelo J Rizzo; Michael P Stone; Thomas M Harris
Journal:  J Am Chem Soc       Date:  2003-01-08       Impact factor: 15.419

9.  Comparative evaluation of the bioreactivity and mutagenic spectra of acrolein-derived alpha-HOPdG and gamma-HOPdG regioisomeric deoxyguanosine adducts.

Authors:  Ana M Sanchez; Irina G Minko; Andrew J Kurtz; Manorama Kanuri; Masaaki Moriya; R Stephen Lloyd
Journal:  Chem Res Toxicol       Date:  2003-08       Impact factor: 3.739

10.  1,N2-deoxyguanosine adducts of acrolein, crotonaldehyde, and trans-4-hydroxynonenal cross-link to peptides via Schiff base linkage.

Authors:  Andrew J Kurtz; R Stephen Lloyd
Journal:  J Biol Chem       Date:  2002-12-26       Impact factor: 5.157

View more
  27 in total

1.  Site-specific synthesis of oligonucleotides containing malondialdehyde adducts of deoxyguanosine and deoxyadenosine via a postsynthetic modification strategy.

Authors:  Hao Wang; Ivan D Kozekov; Albena Kozekova; Pamela J Tamura; Lawrence J Marnett; Thomas M Harris; Carmelo J Rizzo
Journal:  Chem Res Toxicol       Date:  2006-11       Impact factor: 3.739

2.  Unraveling the aflatoxin-FAPY conundrum: structural basis for differential replicative processing of isomeric forms of the formamidopyrimidine-type DNA adduct of aflatoxin B1.

Authors:  Kyle L Brown; James Z Deng; Rajkumar S Iyer; Lalitha G Iyer; Markus W Voehler; Michael P Stone; Constance M Harris; Thomas M Harris
Journal:  J Am Chem Soc       Date:  2006-11-29       Impact factor: 15.419

3.  Multinuclear NMR and kinetic analysis of DNA interstrand cross-link formation.

Authors:  Hui Ding; Ananya Majumdar; Joel R Tolman; Marc M Greenberg
Journal:  J Am Chem Soc       Date:  2008-12-31       Impact factor: 15.419

Review 4.  An overview of chemical processes that damage cellular DNA: spontaneous hydrolysis, alkylation, and reactions with radicals.

Authors:  Kent S Gates
Journal:  Chem Res Toxicol       Date:  2009-11       Impact factor: 3.739

Review 5.  Chemistry and structural biology of DNA damage and biological consequences.

Authors:  Michael P Stone; Hai Huang; Kyle L Brown; Ganesh Shanmugam
Journal:  Chem Biodivers       Date:  2011-09       Impact factor: 2.408

6.  Minor groove orientation of the KWKK peptide tethered via the N-terminal amine to the acrolein-derived 1,N2-gamma-hydroxypropanodeoxyguanosine lesion with a trimethylene linkage.

Authors:  Hai Huang; Ivan D Kozekov; Albena Kozekova; Carmelo J Rizzo; Amanda K McCullough; R Stephen Lloyd; Michael P Stone
Journal:  Biochemistry       Date:  2010-07-27       Impact factor: 3.162

7.  Stereospecific formation of the (R)-gamma-hydroxytrimethylene interstrand N2-dG:N2-dG cross-link arising from the gamma-OH-1,N2-propano-2'-deoxyguanosine adduct in the 5'-CpG-3' DNA sequence.

Authors:  Hai Huang; Hye-Young Kim; Ivan D Kozekov; Young-Jin Cho; Hao Wang; Albena Kozekova; Thomas M Harris; Carmelo J Rizzo; Michael P Stone
Journal:  J Am Chem Soc       Date:  2009-06-24       Impact factor: 15.419

8.  Stereospecific formation of interstrand carbinolamine DNA cross-links by crotonaldehyde- and acetaldehyde-derived alpha-CH3-gamma-OH-1,N2-propano-2'-deoxyguanosine adducts in the 5'-CpG-3' sequence.

Authors:  Young-Jin Cho; Hao Wang; Ivan D Kozekov; Andrew J Kurtz; Jaison Jacob; Markus Voehler; Jarrod Smith; Thomas M Harris; R Stephen Lloyd; Carmelo J Rizzo; Michael P Stone
Journal:  Chem Res Toxicol       Date:  2006-02       Impact factor: 3.739

9.  Interstrand DNA cross-links induced by alpha,beta-unsaturated aldehydes derived from lipid peroxidation and environmental sources.

Authors:  Michael P Stone; Young-Jin Cho; Hai Huang; Hye-Young Kim; Ivan D Kozekov; Albena Kozekova; Hao Wang; Irina G Minko; R Stephen Lloyd; Thomas M Harris; Carmelo J Rizzo
Journal:  Acc Chem Res       Date:  2008-05-24       Impact factor: 22.384

10.  Differential base stacking interactions induced by trimethylene interstrand DNA cross-links in the 5'-CpG-3' and 5'-GpC-3' sequence contexts.

Authors:  Hai Huang; Patricia A Dooley; Constance M Harris; Thomas M Harris; Michael P Stone
Journal:  Chem Res Toxicol       Date:  2009-11       Impact factor: 3.739

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.