The roles of replication-transcription conflict in mutagenesis and evolution of genome organization.

Replication-transcription conflicts promote mutagenesis and give rise to evolutionary signatures, with fundamental importance to genome stability ranging from bacteria to metastatic cancer cells. This review focuses on the interplay between replication-transcription conflicts and the evolution of ge...

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Main Authors: Jeremy W Schroeder, T Sabari Sankar, Jue D Wang, Lyle A Simmons
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-08-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1008987
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spelling doaj-b465f3cc2795484cb30c86c2d7b598f82021-07-04T04:30:59ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042020-08-01168e100898710.1371/journal.pgen.1008987The roles of replication-transcription conflict in mutagenesis and evolution of genome organization.Jeremy W SchroederT Sabari SankarJue D WangLyle A SimmonsReplication-transcription conflicts promote mutagenesis and give rise to evolutionary signatures, with fundamental importance to genome stability ranging from bacteria to metastatic cancer cells. This review focuses on the interplay between replication-transcription conflicts and the evolution of gene directionality. In most bacteria, the majority of genes are encoded on the leading strand of replication such that their transcription is co-directional with the direction of DNA replication fork movement. This gene strand bias arises primarily due to negative selection against deleterious consequences of head-on replication-transcription conflict. However, many genes remain head-on. Can head-on orientation provide some benefit? We combine insights from both mechanistic and evolutionary studies, review published work, and analyze gene expression data to evaluate an emerging model that head-on genes are temporal targets for adaptive mutagenesis during stress. We highlight the alternative explanation that genes in the head-on orientation may simply be the result of genomic inversions and relaxed selection acting on nonessential genes. We seek to clarify how the mechanisms of replication-transcription conflict, in concert with other mutagenic mechanisms, balanced by natural selection, have shaped bacterial genome evolution.https://doi.org/10.1371/journal.pgen.1008987
collection DOAJ
language English
format Article
sources DOAJ
author Jeremy W Schroeder
T Sabari Sankar
Jue D Wang
Lyle A Simmons
spellingShingle Jeremy W Schroeder
T Sabari Sankar
Jue D Wang
Lyle A Simmons
The roles of replication-transcription conflict in mutagenesis and evolution of genome organization.
PLoS Genetics
author_facet Jeremy W Schroeder
T Sabari Sankar
Jue D Wang
Lyle A Simmons
author_sort Jeremy W Schroeder
title The roles of replication-transcription conflict in mutagenesis and evolution of genome organization.
title_short The roles of replication-transcription conflict in mutagenesis and evolution of genome organization.
title_full The roles of replication-transcription conflict in mutagenesis and evolution of genome organization.
title_fullStr The roles of replication-transcription conflict in mutagenesis and evolution of genome organization.
title_full_unstemmed The roles of replication-transcription conflict in mutagenesis and evolution of genome organization.
title_sort roles of replication-transcription conflict in mutagenesis and evolution of genome organization.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2020-08-01
description Replication-transcription conflicts promote mutagenesis and give rise to evolutionary signatures, with fundamental importance to genome stability ranging from bacteria to metastatic cancer cells. This review focuses on the interplay between replication-transcription conflicts and the evolution of gene directionality. In most bacteria, the majority of genes are encoded on the leading strand of replication such that their transcription is co-directional with the direction of DNA replication fork movement. This gene strand bias arises primarily due to negative selection against deleterious consequences of head-on replication-transcription conflict. However, many genes remain head-on. Can head-on orientation provide some benefit? We combine insights from both mechanistic and evolutionary studies, review published work, and analyze gene expression data to evaluate an emerging model that head-on genes are temporal targets for adaptive mutagenesis during stress. We highlight the alternative explanation that genes in the head-on orientation may simply be the result of genomic inversions and relaxed selection acting on nonessential genes. We seek to clarify how the mechanisms of replication-transcription conflict, in concert with other mutagenic mechanisms, balanced by natural selection, have shaped bacterial genome evolution.
url https://doi.org/10.1371/journal.pgen.1008987
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