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Genome Replication in Thermococcus kodakarensis Independent of Cdc6 and an Origin of Replication
The initiation of DNA replication is typically tightly regulated by proteins that form initiation complexes at specific sequences known as replication origins. In Archaea and Eukaryotes, Cdc6, a near-universally conserved protein binds and facilitates the origin-dependent assembly of the replicative...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663688/ https://www.ncbi.nlm.nih.gov/pubmed/29163389 http://dx.doi.org/10.3389/fmicb.2017.02084 |
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author | Gehring, Alexandra M. Astling, David P. Matsumi, Rie Burkhart, Brett W. Kelman, Zvi Reeve, John N. Jones, Kenneth L. Santangelo, Thomas J. |
author_facet | Gehring, Alexandra M. Astling, David P. Matsumi, Rie Burkhart, Brett W. Kelman, Zvi Reeve, John N. Jones, Kenneth L. Santangelo, Thomas J. |
author_sort | Gehring, Alexandra M. |
collection | PubMed |
description | The initiation of DNA replication is typically tightly regulated by proteins that form initiation complexes at specific sequences known as replication origins. In Archaea and Eukaryotes, Cdc6, a near-universally conserved protein binds and facilitates the origin-dependent assembly of the replicative apparatus. TK1901 encodes Cdc6 in Thermococcus kodakarensis but, as we report here, TK1901 and the presumed origin of replication can be deleted from the genome of this hyperthermophilic Archaeon without any detectable effects on growth, genetic competence or the ability to support autonomous plasmid replication. All regions of the genome were equally represented in the sequences generated by whole genome sequencing of DNA isolated from T. kodakarensis strains with or without TK1901, inconsistent with DNA initiation occurring at one or few origins, and instead suggestive of replication initiating at many sites distributed throughout the genome. We were unable to generate strains lacking the recombination factors, RadA or RadB, consistent with T. kodakarensis cells, that are oligoploid (7–19 genomes per cell), employing a recombination-based mechanism of DNA replication. Deletion of the previously presumed origin region reduced the long-term viability of cultures supporting the possibility that retaining an origin-based mechanism of DNA initiation provides a survival mechanism for stationary phase cells with only one genome. |
format | Online Article Text |
id | pubmed-5663688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56636882017-11-21 Genome Replication in Thermococcus kodakarensis Independent of Cdc6 and an Origin of Replication Gehring, Alexandra M. Astling, David P. Matsumi, Rie Burkhart, Brett W. Kelman, Zvi Reeve, John N. Jones, Kenneth L. Santangelo, Thomas J. Front Microbiol Microbiology The initiation of DNA replication is typically tightly regulated by proteins that form initiation complexes at specific sequences known as replication origins. In Archaea and Eukaryotes, Cdc6, a near-universally conserved protein binds and facilitates the origin-dependent assembly of the replicative apparatus. TK1901 encodes Cdc6 in Thermococcus kodakarensis but, as we report here, TK1901 and the presumed origin of replication can be deleted from the genome of this hyperthermophilic Archaeon without any detectable effects on growth, genetic competence or the ability to support autonomous plasmid replication. All regions of the genome were equally represented in the sequences generated by whole genome sequencing of DNA isolated from T. kodakarensis strains with or without TK1901, inconsistent with DNA initiation occurring at one or few origins, and instead suggestive of replication initiating at many sites distributed throughout the genome. We were unable to generate strains lacking the recombination factors, RadA or RadB, consistent with T. kodakarensis cells, that are oligoploid (7–19 genomes per cell), employing a recombination-based mechanism of DNA replication. Deletion of the previously presumed origin region reduced the long-term viability of cultures supporting the possibility that retaining an origin-based mechanism of DNA initiation provides a survival mechanism for stationary phase cells with only one genome. Frontiers Media S.A. 2017-10-27 /pmc/articles/PMC5663688/ /pubmed/29163389 http://dx.doi.org/10.3389/fmicb.2017.02084 Text en Copyright © 2017 Gehring, Astling, Matsumi, Burkhart, Kelman, Reeve, Jones and Santangelo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Gehring, Alexandra M. Astling, David P. Matsumi, Rie Burkhart, Brett W. Kelman, Zvi Reeve, John N. Jones, Kenneth L. Santangelo, Thomas J. Genome Replication in Thermococcus kodakarensis Independent of Cdc6 and an Origin of Replication |
title | Genome Replication in Thermococcus kodakarensis Independent of Cdc6 and an Origin of Replication |
title_full | Genome Replication in Thermococcus kodakarensis Independent of Cdc6 and an Origin of Replication |
title_fullStr | Genome Replication in Thermococcus kodakarensis Independent of Cdc6 and an Origin of Replication |
title_full_unstemmed | Genome Replication in Thermococcus kodakarensis Independent of Cdc6 and an Origin of Replication |
title_short | Genome Replication in Thermococcus kodakarensis Independent of Cdc6 and an Origin of Replication |
title_sort | genome replication in thermococcus kodakarensis independent of cdc6 and an origin of replication |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663688/ https://www.ncbi.nlm.nih.gov/pubmed/29163389 http://dx.doi.org/10.3389/fmicb.2017.02084 |
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