Literature DB >> 15145803

Transcription/replication collisions cause bacterial transcription units to be longer on the leading strand of replication.

Nicolas Omont1, François Képès.   

Abstract

MOTIVATION: The costs of head-on versus codirectional collisions between the replication complex and the much slower transcription complex on the circular bacterial chromosomes are much debated. Although it is established that the number of genes on the leading strand is higher than on the lagging strand of replication, the consequences of collisions on the length of transcription units are unknown.
RESULTS: Here, we show that transcription units are generally longer on the leading strand, in rough proportion to the bias in number of units between the two strands. We propose a statistical physics model, based on the assumption that the proportion of interrupted transcripts for each unit is the major factor contributing to these biases. Its main prediction is that a large replication/transcription speed ratio implies a low leading/lagging bias for transcription unit length and number. This model is validated by an analysis of proven and predicted units in Escherichia coli and Bacillus subtilis. The results are consistent with an equal cost of head-on versus codirectional collisions.

Entities:  

Mesh:

Year:  2004        PMID: 15145803     DOI: 10.1093/bioinformatics/bth317

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  18 in total

Review 1.  What happens when replication and transcription complexes collide?

Authors:  Richard T Pomerantz; Mike O'Donnell
Journal:  Cell Cycle       Date:  2010-07-01       Impact factor: 4.534

2.  Genome-wide coorientation of replication and transcription reduces adverse effects on replication in Bacillus subtilis.

Authors:  Jue D Wang; Melanie B Berkmen; Alan D Grossman
Journal:  Proc Natl Acad Sci U S A       Date:  2007-03-19       Impact factor: 11.205

Review 3.  Mechanisms and evolution of control logic in prokaryotic transcriptional regulation.

Authors:  Sacha A F T van Hijum; Marnix H Medema; Oscar P Kuipers
Journal:  Microbiol Mol Biol Rev       Date:  2009-09       Impact factor: 11.056

Review 4.  Does the Semiconservative Nature of DNA Replication Facilitate Coherent Phenotypic Diversity?

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Journal:  J Bacteriol       Date:  2019-05-22       Impact factor: 3.490

5.  Spatial and Temporal Control of Evolution through Replication-Transcription Conflicts.

Authors:  Houra Merrikh
Journal:  Trends Microbiol       Date:  2017-02-16       Impact factor: 17.079

6.  Hypothesis: nucleoid-associated proteins segregate with a parental DNA strand to generate coherent phenotypic diversity.

Authors:  Yoan Konto-Ghiorghi; Vic Norris
Journal:  Theory Biosci       Date:  2020-10-23       Impact factor: 1.919

7.  Chromosomal periodicity and positional networks of genes in Escherichia coli.

Authors:  Anthony Mathelier; Alessandra Carbone
Journal:  Mol Syst Biol       Date:  2010-05-11       Impact factor: 11.429

Review 8.  Coevolution of the Organization and Structure of Prokaryotic Genomes.

Authors:  Marie Touchon; Eduardo P C Rocha
Journal:  Cold Spring Harb Perspect Biol       Date:  2016-01-04       Impact factor: 10.005

9.  Co-orientation of replication and transcription preserves genome integrity.

Authors:  Anjana Srivatsan; Ashley Tehranchi; David M MacAlpine; Jue D Wang
Journal:  PLoS Genet       Date:  2010-01-15       Impact factor: 5.917

10.  A blueprint for a mutationist theory of replicative strand asymmetries formation.

Authors:  Vladislav V Khrustalev; Eugene V Barkovsky
Journal:  Curr Genomics       Date:  2012-03       Impact factor: 2.236

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