Home LiteratureArticle Details
PMID: 11148050 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Non-oxidative mechanisms are responsible for the induction of mutagenesis by reduction of Cr(VI) with cysteine: role of ternary DNA adducts in Cr(III)-dependent mutagenesis.

Biochemistry ·Vol. 40 ·No. 2 ·2001-01-16 ·Pages 549-60

Zhitkovich A, Song Y, Quievryn G, Voitkun V

Abstract

Intracellular reduction of carcinogenic Cr(VI) generates Cr-DNA adducts formed through the coordination of Cr(III) to DNA phosphates (phosphotriester-type adduct). Here, we examined the role of Cr(III)-DNA adducts in mutagenesis induced by metabolism of Cr(VI) with cysteine. Reduction of Cr(VI) caused a strong oxidation of 2', 7'-dichlorofluoroscin (DCFH) and extensive Cr-DNA binding but no DNA breakage. Cr-DNA adducts induced unwinding of supercoiled plasmids and structural distortions in the DNA helix as detected by decreased ethidium bromide binding. Propagation of Cr-treated pSP189 plasmids in human fibroblasts led to a dose-dependent formation of the supF mutants and inhibition of replication. Blocking of Cr(III)-DNA binding by occupation of DNA phosphates with Mg(2+) or by sequestration of Cr(III) by inorganic phosphate or EDTA eliminated mutagenic responses and restored a normal yield of replicated plasmids. Dissociation of Cr(III) from DNA by a phosphate-based reversal procedure returned mutation frequency to background levels. The mutagenic responses at the different phases of the reduction reaction were unrelated to the amount of reduced Cr(VI) but reflected the number and the spectrum of Cr(III)-DNA adducts that were formed. Ternary cysteine-Cr(III)-DNA adducts were approximately 4-5 times more mutagenic than binary Cr(III)-DNA adducts. Although intermediate reaction products (CrV/IV, thiyl radicals) were capable of oxidizing DCFH, they were insufficiently reactive to damage DNA. Single-base substitutions at G/C pairs were the predominant type of Cr-induced mutations. The majority of mutations occurred at the sites where G had adjacent purine in the 3' or 5' position. Overall, our results present the first evidence that Cr(III)-DNA adducts play the dominant role in the mutagenicity caused by the metabolism of Cr(VI) by a biological reducing agent.

MeSH Terms
Base Sequence Carcinogens, Environmental/chemistry,metabolism Cell Line, Transformed Chromium/chemistry,metabolism Cysteine/chemistry,metabolism DNA Adducts/biosynthesis,chemistry,metabolism DNA Damage DNA Mutational Analysis Fluoresceins/metabolism Genes, Suppressor Genetic Vectors/chemistry,metabolism Humans Molecular Sequence Data Morpholines/metabolism Mutagenesis Oxidation-Reduction RNA, Transfer/chemistry,genetics Reducing Agents/chemistry,metabolism
Chemicals
Carcinogens, Environmental DNA Adducts Fluoresceins Morpholines Reducing Agents supF tRNA Chromium 2',7'-dichlorodihydrofluorescein chromium hexavalent ion morpholinopropane sulfonic acid RNA, Transfer Cysteine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Zhitkovich A
Brown University, Department of Pathology and Laboratory Medicine, Providence, Rhode Island 02912, USA. [email protected]
Song Y
Quievryn G
Voitkun V
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
2001-01-16
Pages
549-60
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIEHS NIH HHS · R01 ES008786 · United States
NIEHS NIH HHS · ES 08786 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]