Literature DB >> 28842872

Measuring In Vivo Supercoil Dynamics and Transcription Elongation Rates in Bacterial Chromosomes.

N Patrick Higgins1.   

Abstract

DNA gyrase is the only topoisomerase that can catalytically introduce negative supercoils into covalently closed DNA. The enzyme plays a critical role in many phases of DNA biochemistry. There are only a few methods that allow one to measure supercoiling in chromosomal DNA and analyze the role of gyrase in transcription and its interaction with the other three bacterial topoisomerases. Here, we provide molecular tools for measuring supercoil density in the chromosome and for connecting the dots between transcription and DNA topology.

Entities:  

Keywords:  Chromosome; Gyrase; Resolvase; Salmonella; Supercoiling; Transcription

Mesh:

Substances:

Year:  2017        PMID: 28842872     DOI: 10.1007/978-1-4939-7098-8_2

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  3 in total

1.  FEDS: a Novel Fluorescence-Based High-Throughput Method for Measuring DNA Supercoiling In Vivo.

Authors:  Alexandre Duprey; Eduardo A Groisman
Journal:  mBio       Date:  2020-07-28       Impact factor: 7.867

2.  DNA supercoiling differences in bacteria result from disparate DNA gyrase activation by polyamines.

Authors:  Alexandre Duprey; Eduardo A Groisman
Journal:  PLoS Genet       Date:  2020-10-30       Impact factor: 5.917

3.  High-resolution, genome-wide mapping of positive supercoiling in chromosomes.

Authors:  Monica S Guo; Ryo Kawamura; Megan L Littlehale; John F Marko; Michael T Laub
Journal:  Elife       Date:  2021-07-19       Impact factor: 8.140

  3 in total

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