Literature DB >> 31379009

Half-Intercalation Stabilizes Slipped Mispairing and Explains Genome Vulnerability to Frameshift Mutagenesis by Endogenous "Molecular Bookmarks".

Andrei Kuzminov1.   

Abstract

Some 60 years ago chemicals that intercalate between base pairs of duplex DNA were found to amplify frameshift mutagenesis. Surprisingly, the robust induction of frameshifts by intercalators still lacks a mechanistic model, leaving this classic phenomenon annoyingly intractable. A promising idea of asymmetric half-intercalation-stabilizing frameshift intermediates during DNA synthesis has never been developed into a model. Instead, researchers of frameshift mutagenesis embraced the powerful slipped-mispairing concept that unexpectedly struggled with the role of intercalators in frameshifting. It is proposed that the slipped mispairing and the half-intercalation ideas are two sides of the same coin. Further, existing findings are reviewed to test predictions of the combined "half-intercalation into the slipped-mispairing intermediate" model against accumulated knowledge. The existence of potential endogenous intercalators and the phenomenon of "DNA bookmarks" reveal ample possibilities for natural frameshift mutagenisis in the cell. From this alarming perspective, it is discussed how the cell could prevent genome deterioration from frameshift mutagenesis.
© 2019 WILEY Periodicals, Inc.

Entities:  

Keywords:  1 base pair (bp) indels; DNA synthesis; acridines; asymmetric intercalations; ethidium bromide; strand slippage

Mesh:

Substances:

Year:  2019        PMID: 31379009      PMCID: PMC6707839          DOI: 10.1002/bies.201900062

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  96 in total

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Authors:  L S LERMAN
Journal:  Proc Natl Acad Sci U S A       Date:  1963-01-15       Impact factor: 11.205

2.  Fidelity of Escherichia coli DNA polymerase III holoenzyme. The effects of beta, gamma complex processivity proteins and epsilon proofreading exonuclease on nucleotide misincorporation efficiencies.

Authors:  L B Bloom; X Chen; D K Fygenson; J Turner; M O'Donnell; M F Goodman
Journal:  J Biol Chem       Date:  1997-10-31       Impact factor: 5.157

Review 3.  Frameshift mutations.

Authors:  J R Roth
Journal:  Annu Rev Genet       Date:  1974       Impact factor: 16.830

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Authors:  G G Revich; L S Ripley
Journal:  J Mol Biol       Date:  1990-01-05       Impact factor: 5.469

5.  Frameshift mutagenesis of lambda prophage by 9-aminoacridine, proflavin and ICR-191.

Authors:  T R Skopek; F Hutchinson
Journal:  Mol Gen Genet       Date:  1984

6.  Binding of 9-aminoacridine to deoxydinucleoside phosphates of defined sequence: preferences and stereochemistry.

Authors:  P R Young; N R Kallenbach
Journal:  J Mol Biol       Date:  1981-02-05       Impact factor: 5.469

7.  Action of intercalating agents on the activity of DNA polymerase I.

Authors:  R Böhner; U Hagen
Journal:  Biochim Biophys Acta       Date:  1977-12-02

8.  Binding of 9-aminoacridine to bulged-base DNA oligomers from a frame-shift hot spot.

Authors:  S A Woodson; D M Crothers
Journal:  Biochemistry       Date:  1988-12-13       Impact factor: 3.162

9.  Neocarzinostatin chromophore. Assignment of spectral properties and structural requirements for binding to DNA.

Authors:  M A Napier; I H Goldberg
Journal:  Mol Pharmacol       Date:  1983-03       Impact factor: 4.436

10.  Mutagen-nucleic acid intercalative binding: structure of a 9-aminoacridine: 5-iodocytidylyl(3'-5')guanosine crystalline complex.

Authors:  T D Sakore; S C Jain; C C Tsai; H M Sobell
Journal:  Proc Natl Acad Sci U S A       Date:  1977-01       Impact factor: 11.205

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