Literature DB >> 8950269

Relationship between Escherichia coli growth and deletions of CTG.CAG triplet repeats in plasmids.

R P Bowater1, W A Rosche, A Jaworski, R R Sinden, R D Wells.   

Abstract

Instabilities that are intrinsic to natural repetitive DNA sequences produce high frequencies of length changes in vivo. Triplet repeats cloned in plasmids in Escherichia coli undergo expansions and deletions, and this instability is affected by multiple factors. We show that CTG-CAG repeats in plasmids can influence the growth of E. coli, which affects the observed stabilities. At extended growth periods, the observed frequencies of deletions were dramatically increased if the cells passed through stationary phase before subculturing. Deletions were particularly pronounced for a plasmid containing the longest repeat, 525 bp in total, with the CTG sequence as the lagging strand template for replication. Measurements of cell growth showed that the lag phase associated with E. coli growth was increased for cultures containing plasmids with long CTG-CAG repeats, particularly when the CTG-containing strand was the lagging template. High frequencies of deletions were observed because of a growth advantage of cells containing plasmids with deleted triplet repeats. Incubation conditions that reduced the bacterial growth-rate produced a decreased extent of deletions, presumably because they alleviated the growth advantage of cells harboring plasmids with deleted triplet repeats. The experimental observations were simulated by a model in which shorter triplet repeats provided a growth advantage due to a shorter lag phase. We demonstrate that the accumulation of deletions within repeating sequences during growth of E. coli can be prevented, and discuss these findings in relation to the studies of repetitive DNA sequences. These are the first observations to show a direct influence between a plasmid-based DNA sequence or structure and factors controlling bacterial growth.

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Year:  1996        PMID: 8950269     DOI: 10.1006/jmbi.1996.0625

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  18 in total

1.  CpG methylation modifies the genetic stability of cloned repeat sequences.

Authors:  Kerrie Nichol; Christopher E Pearson
Journal:  Genome Res       Date:  2002-08       Impact factor: 9.043

2.  Transcription increases the deletion frequency of long CTG.CAG triplet repeats from plasmids in Escherichia coli.

Authors:  R P Bowater; A Jaworski; J E Larson; P Parniewski; R D Wells
Journal:  Nucleic Acids Res       Date:  1997-07-15       Impact factor: 16.971

3.  E. coli mismatch repair acts downstream of replication fork stalling to stabilize the expanded (GAA.TTC)(n) sequence.

Authors:  Rebecka L Bourn; Paul M Rindler; Laura M Pollard; Sanjay I Bidichandani
Journal:  Mutat Res       Date:  2008-11-13       Impact factor: 2.433

4.  The role of SOS and flap processing in microsatellite instability in Escherichia coli.

Authors:  P Morel; C Reverdy; B Michel; S D Ehrlich; E Cassuto
Journal:  Proc Natl Acad Sci U S A       Date:  1998-08-18       Impact factor: 11.205

5.  Structural analysis of slipped-strand DNA (S-DNA) formed in (CTG)n. (CAG)n repeats from the myotonic dystrophy locus.

Authors:  C E Pearson; Y H Wang; J D Griffith; R R Sinden
Journal:  Nucleic Acids Res       Date:  1998-02-01       Impact factor: 16.971

6.  Conformational energetics of stable and metastable states formed by DNA triplet repeat oligonucleotides: implications for triplet expansion diseases.

Authors:  J Völker; N Makube; G E Plum; H H Klump; K J Breslauer
Journal:  Proc Natl Acad Sci U S A       Date:  2002-11-04       Impact factor: 11.205

Review 7.  Expanded complexity of unstable repeat diseases.

Authors:  Urszula Polak; Elizabeth McIvor; Sharon Y R Dent; Robert D Wells; Marek Napierala
Journal:  Biofactors       Date:  2012-12-11       Impact factor: 6.113

Review 8.  DNA triplet repeat expansion and mismatch repair.

Authors:  Ravi R Iyer; Anna Pluciennik; Marek Napierala; Robert D Wells
Journal:  Annu Rev Biochem       Date:  2015-01-02       Impact factor: 23.643

9.  Potassium bromate, a potent DNA oxidizing agent, exacerbates germline repeat expansion in a fragile X premutation mouse model.

Authors:  Ali Entezam; Adihe Rachel Lokanga; Wei Le; Gloria Hoffman; Karen Usdin
Journal:  Hum Mutat       Date:  2010-05       Impact factor: 4.878

10.  Transcription influences the types of deletion and expansion products in an orientation-dependent manner from GAC*GTC repeats.

Authors:  Liliana H Mochmann; Robert D Wells
Journal:  Nucleic Acids Res       Date:  2004-08-18       Impact factor: 16.971

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