Literature DB >> 26733364

Conformational Insights into the Mechanism of Acetylaminofluorene-dG-Induced Frameshift Mutations in the NarI Mutational Hotspot.

Lifang Xu1, Bongsup P Cho1.   

Abstract

Frameshift mutagenesis encompasses the gain or loss of DNA base pairs, resulting in altered genetic outcomes. The NarI restriction site sequence 5'-G1G2CG3CX-3' in Escherichia coli is a well-known mutational hotspot, in which lesioning of acetylaminofluorene (AAF) at G3* induces a greater -2 deletion frequency than that at other guanine sites. Its mutational efficiency is modulated by the nature of the nucleotide in the X position (C ∼ A > G ≫ T). Here, we conducted a series of polymerase-free solution experiments that examine the conformational and thermodynamic basis underlying the propensity of adducted G3 to form a slipped mutagenic intermediate (SMI) and its sequence dependence during translesion synthesis (TLS). Instability of the AAF-dG3:dC pair at the replication fork promoted slippage to form a G*C bulge-out SMI structure, consisting of S- ("lesion stacked") and B-SMI ("lesion exposed") conformations, with conformational rigidity increasing as a function of primer elongation. We found greater stability of the S- compared to the B-SMI conformer throughout TLS. The dependence of their population ratios was determined by the 3'-next flanking base X at fully elongated bulge structures, with 59% B/41% S and 86% B/14% S for the dC and dT series, respectively. These results indicate the importance of direct interactions of the hydrophobic AAF lesion with the 3'-next flanking base pair and its stacking fit within the -2 bulge structure. A detailed conformational understanding of the SMI structures and their sequence dependence may provide a useful model for DNA polymerase complexes.

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Year:  2016        PMID: 26733364      PMCID: PMC6775635          DOI: 10.1021/acs.chemrestox.5b00484

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  55 in total

1.  Probing the thermodynamics of aminofluorene-induced translesion DNA synthesis by differential scanning calorimetry.

Authors:  Fengting Liang; Bongsup P Cho
Journal:  J Am Chem Soc       Date:  2007-09-15       Impact factor: 15.419

2.  Mutagenic specificity of (acetylamino)fluorene-derived DNA adducts in mammalian cells.

Authors:  S Shibutani; N Suzuki; A P Grollman
Journal:  Biochemistry       Date:  1998-09-01       Impact factor: 3.162

Review 3.  Mutagenic specificity of chemical carcinogens as determined by studies of single DNA adducts.

Authors:  A P Grollman; S Shibutani
Journal:  IARC Sci Publ       Date:  1994

4.  Accommodation of an N-(deoxyguanosin-8-yl)-2-acetylaminofluorene adduct in the active site of human DNA polymerase iota: Hoogsteen or Watson-Crick base pairing?

Authors:  Kerry Donny-Clark; Robert Shapiro; Suse Broyde
Journal:  Biochemistry       Date:  2009-01-13       Impact factor: 3.162

5.  Observing translesion synthesis of an aromatic amine DNA adduct by a high-fidelity DNA polymerase.

Authors:  Gerald W Hsu; James R Kiefer; Dominique Burnouf; Olivier J Becherel; Robert P P Fuchs; Lorena S Beese
Journal:  J Biol Chem       Date:  2004-09-22       Impact factor: 5.157

6.  Mechanistic Basis for the Bypass of a Bulky DNA Adduct Catalyzed by a Y-Family DNA Polymerase.

Authors:  Rajan Vyas; Georgia Efthimiopoulos; E John Tokarsky; Chanchal K Malik; Ashis K Basu; Zucai Suo
Journal:  J Am Chem Soc       Date:  2015-09-11       Impact factor: 15.419

7.  NMR data show that the carcinogen N-2-acetylaminofluorene stabilises an intermediate of -2 frameshift mutagenesis in a region of high mutation frequency.

Authors:  C Milhé; R P Fuchs; J F Lefèvre
Journal:  Eur J Biochem       Date:  1996-01-15

Review 8.  Nitroaromatic compounds: Environmental toxicity, carcinogenicity, mutagenicity, therapy and mechanism.

Authors:  Peter Kovacic; Ratnasamy Somanathan
Journal:  J Appl Toxicol       Date:  2014-02-16       Impact factor: 3.446

9.  Conformational and thermodynamic properties modulate the nucleotide excision repair of 2-aminofluorene and 2-acetylaminofluorene dG adducts in the NarI sequence.

Authors:  Vipin Jain; Benjamin Hilton; Satyakam Patnaik; Yue Zou; M Paul Chiarelli; Bongsup P Cho
Journal:  Nucleic Acids Res       Date:  2012-01-12       Impact factor: 16.971

10.  Conformational insights into the lesion and sequence effects for arylamine-induced translesion DNA synthesis: 19F NMR, surface plasmon resonance, and primer kinetic studies.

Authors:  Vipin Jain; Vaidyanathan G Vaidyanathan; Satyakam Patnaik; Sathyaraj Gopal; Bongsup P Cho
Journal:  Biochemistry       Date:  2014-06-10       Impact factor: 3.162

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  2 in total

1.  Switch-on effect on conformation-specific arylamine-DNA adduct by cyclometalated Ir(III) complexes.

Authors:  David Dayanidhi Paul Elisa; Vaidyanathan Vaidyanathan Ganesan
Journal:  J Biol Inorg Chem       Date:  2020-02-12       Impact factor: 3.358

2.  DNA base sequence effects on bulky lesion-induced conformational heterogeneity during DNA replication.

Authors:  Ang Cai; Katie A Wilson; Satyakam Patnaik; Stacey D Wetmore; Bongsup P Cho
Journal:  Nucleic Acids Res       Date:  2018-07-06       Impact factor: 16.971

  2 in total

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