Literature DB >> 11243802

Modulation of transcription reveals a new mechanism of triplet repeat instability in Escherichia coli.

S Schumacher1, I Pinet, M Bichara.   

Abstract

Many human hereditary disease genes are associated with the expansion of triplet repeat sequences. In Escherichia coli (CTG/CAG) triplet repeat sequences are unstable and we have developed a plasmid-based assay enabling us to observe and quantify both expansions and deletions. In this work, we have investigated the role of transcription on the instability of a (CTG/CAG) insert containing 64 repeats. Using this assay, we show that induction of transcription results in a significant increase in the frequency of long deletions and a reduction in the frequency of long expansions. On the other hand, overproduction of transcription repressor molecules leads to an increase in both expansions and deletions. In this latter case, we propose that the increased instability is due to the arrest of replication progression by the interaction of the repressor molecule with its cognate operator and subsequent generations of DNA strand breaks. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11243802     DOI: 10.1006/jmbi.2000.4489

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


  13 in total

1.  Diverse effects of individual mismatch repair components on transcription-induced CAG repeat instability in human cells.

Authors:  Yunfu Lin; John H Wilson
Journal:  DNA Repair (Amst)       Date:  2009-06-03

Review 2.  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

3.  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

4.  Xpa deficiency reduces CAG trinucleotide repeat instability in neuronal tissues in a mouse model of SCA1.

Authors:  Leroy Hubert; Yunfu Lin; Vincent Dion; John H Wilson
Journal:  Hum Mol Genet       Date:  2011-09-15       Impact factor: 6.150

5.  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

6.  Somatic expansion in mouse and human carriers of fragile X premutation alleles.

Authors:  Rachel Adihe Lokanga; Ali Entezam; Daman Kumari; Dmitry Yudkin; Mei Qin; Carolyn Beebe Smith; Karen Usdin
Journal:  Hum Mutat       Date:  2012-10-04       Impact factor: 4.878

7.  Transcription-induced CAG repeat contraction in human cells is mediated in part by transcription-coupled nucleotide excision repair.

Authors:  Yunfu Lin; John H Wilson
Journal:  Mol Cell Biol       Date:  2007-06-25       Impact factor: 4.272

8.  Long CTG tracts from the myotonic dystrophy gene induce deletions and rearrangements during recombination at the APRT locus in CHO cells.

Authors:  James L Meservy; R Geoffrey Sargent; Ravi R Iyer; Fung Chan; Gregory J McKenzie; Robert D Wells; John H Wilson
Journal:  Mol Cell Biol       Date:  2003-05       Impact factor: 4.272

9.  Selectable system for monitoring the instability of CTG/CAG triplet repeats in mammalian cells.

Authors:  Vera Gorbunova; Andrei Seluanov; Vincent Dion; Zoltan Sandor; James L Meservy; John H Wilson
Journal:  Mol Cell Biol       Date:  2003-07       Impact factor: 4.272

10.  Proofreading and secondary structure processing determine the orientation dependence of CAG x CTG trinucleotide repeat instability in Escherichia coli.

Authors:  Rabaab Zahra; John K Blackwood; Jill Sales; David R F Leach
Journal:  Genetics       Date:  2007-03-04       Impact factor: 4.562

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