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Identification of a basal system for unwinding a bacterial chromosome origin
Genome duplication is essential for cell proliferation, and DNA synthesis is generally initiated by dedicated replication proteins at specific loci termed origins. In bacteria, the master initiator DnaA binds the chromosome origin (oriC) and unwinds the DNA duplex to permit helicase loading. However...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669920/ https://www.ncbi.nlm.nih.gov/pubmed/31267560 http://dx.doi.org/10.15252/embj.2019101649 |
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author | Richardson, Tomas T Stevens, Daniel Pelliciari, Simone Harran, Omar Sperlea, Theodor Murray, Heath |
author_facet | Richardson, Tomas T Stevens, Daniel Pelliciari, Simone Harran, Omar Sperlea, Theodor Murray, Heath |
author_sort | Richardson, Tomas T |
collection | PubMed |
description | Genome duplication is essential for cell proliferation, and DNA synthesis is generally initiated by dedicated replication proteins at specific loci termed origins. In bacteria, the master initiator DnaA binds the chromosome origin (oriC) and unwinds the DNA duplex to permit helicase loading. However, despite decades of research it remained unclear how the information encoded within oriC guides DnaA‐dependent strand separation. To address this fundamental question, we took a systematic genetic approach in vivo and identified the core set of essential sequence elements within the Bacillus subtilis chromosome origin unwinding region. Using this information, we then show in vitro that the minimal replication origin sequence elements are necessary and sufficient to promote the mechanical functions of DNA duplex unwinding by DnaA. Because the basal DNA unwinding system characterized here appears to be conserved throughout the bacterial domain, this discovery provides a framework for understanding oriC architecture, activity, regulation and diversity. |
format | Online Article Text |
id | pubmed-6669920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66699202019-08-06 Identification of a basal system for unwinding a bacterial chromosome origin Richardson, Tomas T Stevens, Daniel Pelliciari, Simone Harran, Omar Sperlea, Theodor Murray, Heath EMBO J Articles Genome duplication is essential for cell proliferation, and DNA synthesis is generally initiated by dedicated replication proteins at specific loci termed origins. In bacteria, the master initiator DnaA binds the chromosome origin (oriC) and unwinds the DNA duplex to permit helicase loading. However, despite decades of research it remained unclear how the information encoded within oriC guides DnaA‐dependent strand separation. To address this fundamental question, we took a systematic genetic approach in vivo and identified the core set of essential sequence elements within the Bacillus subtilis chromosome origin unwinding region. Using this information, we then show in vitro that the minimal replication origin sequence elements are necessary and sufficient to promote the mechanical functions of DNA duplex unwinding by DnaA. Because the basal DNA unwinding system characterized here appears to be conserved throughout the bacterial domain, this discovery provides a framework for understanding oriC architecture, activity, regulation and diversity. John Wiley and Sons Inc. 2019-06-27 2019-08-01 /pmc/articles/PMC6669920/ /pubmed/31267560 http://dx.doi.org/10.15252/embj.2019101649 Text en © 2019 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Richardson, Tomas T Stevens, Daniel Pelliciari, Simone Harran, Omar Sperlea, Theodor Murray, Heath Identification of a basal system for unwinding a bacterial chromosome origin |
title | Identification of a basal system for unwinding a bacterial chromosome origin |
title_full | Identification of a basal system for unwinding a bacterial chromosome origin |
title_fullStr | Identification of a basal system for unwinding a bacterial chromosome origin |
title_full_unstemmed | Identification of a basal system for unwinding a bacterial chromosome origin |
title_short | Identification of a basal system for unwinding a bacterial chromosome origin |
title_sort | identification of a basal system for unwinding a bacterial chromosome origin |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669920/ https://www.ncbi.nlm.nih.gov/pubmed/31267560 http://dx.doi.org/10.15252/embj.2019101649 |
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