Literature DB >> 1865910

Preferential DNA secondary structure mutagenesis in the lagging strand of replication in E. coli.

T Q Trinh1, R R Sinden.   

Abstract

When present in single-stranded DNA, palindromic or quasi-palindromic sequences have the potential to form complex secondary structures, including hairpins, which may facilitate interstrand misalignment of direct repeats and be responsible for diverse types of replication-based mutations, including deletions, additions, frameshifts and duplications. In regions of palindromic symmetry, specific deletion events may involve the formation of a hairpin or other DNA secondary structures which can stabilize the misalignment of direct repeats. One model suggests that these deletions occur during DNA replication by slippage of the template strand and misalignment with the progeny strand. The concurrent DNA replication model, involving an asymmetric dimeric DNA polymerase III complex which replicates the leading and lagging strands, has significant implications for mutagenesis. The intermittent looping of the lagging strand template, and the fact that the lagging strand template may contain a region of single-stranded DNA the length of an Okazaki fragment, provides an opportunity for DNA secondary-structure formation and misalignment. Here we report our design of a palindromic fragment to create an 'asymmetric palindromic insert' in the chloramphenicol acetyltransferase gene of plasmid pBR325. The frequency with which the insert was deleted in Escherichia coli depends on the orientation of the gene in the plasmid. Our results suggest that replication-dependent deletion between direct repeats may occur preferentially in the lagging strand.

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Year:  1991        PMID: 1865910     DOI: 10.1038/352544a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  95 in total

1.  Palindromes as substrates for multiple pathways of recombination in Escherichia coli.

Authors:  G A Cromie; C B Millar; K H Schmidt; D R Leach
Journal:  Genetics       Date:  2000-02       Impact factor: 4.562

2.  The roles of mutS, sbcCD and recA in the propagation of TGG repeats in Escherichia coli.

Authors:  X Pan; D R Leach
Journal:  Nucleic Acids Res       Date:  2000-08-15       Impact factor: 16.971

3.  Instability of repetitive DNA sequences: the role of replication in multiple mechanisms.

Authors:  M Bzymek; S T Lovett
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

4.  Evidence for two mechanisms of palindrome-stimulated deletion in Escherichia coli: single-strand annealing and replication slipped mispairing.

Authors:  M Bzymek; S T Lovett
Journal:  Genetics       Date:  2001-06       Impact factor: 4.562

5.  A 160-bp palindrome is a Rad50.Rad32-dependent mitotic recombination hotspot in Schizosaccharomyces pombe.

Authors:  Joseph A Farah; Edgar Hartsuiker; Ken-Ichi Mizuno; Kunihiro Ohta; Gerald R Smith
Journal:  Genetics       Date:  2002-05       Impact factor: 4.562

Review 6.  Role of inverted DNA repeats in transcriptional and post-transcriptional gene silencing.

Authors:  M W Muskens; A P Vissers; J N Mol; J M Kooter
Journal:  Plant Mol Biol       Date:  2000-06       Impact factor: 4.076

7.  Cloning and characterization of the region III flagellar operons of the four Shigella subgroups: genetic defects that cause loss of flagella of Shigella boydii and Shigella sonnei.

Authors:  A A Al Mamun; A Tominaga; M Enomoto
Journal:  J Bacteriol       Date:  1997-07       Impact factor: 3.490

8.  In vitro expansion of mammalian telomere repeats by DNA polymerase alpha-primase.

Authors:  K Nozawa; M Suzuki; M Takemura; S Yoshida
Journal:  Nucleic Acids Res       Date:  2000-08-15       Impact factor: 16.971

9.  Chemotherapeutic deletion of CTG repeats in lymphoblast cells from DM1 patients.

Authors:  Vera I Hashem; Malgorzata J Pytlos; Elzbieta A Klysik; Kuniko Tsuji; Mehrdad Khajavi; Merhdad Khajav; Tetsuo Ashizawa; Richard R Sinden
Journal:  Nucleic Acids Res       Date:  2004-12-01       Impact factor: 16.971

10.  C1 inhibitor gene sequence facilitates frameshift mutations.

Authors:  J J Bissler; Q S Meng; T Emery
Journal:  Mol Med       Date:  1998-12       Impact factor: 6.354

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