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The Borrelia burgdorferi telomere resolvase, ResT, possesses ATP-dependent DNA unwinding activity

Spirochetes of the genus Borrelia possess unusual genomes harboring multiple linear and circular replicons. The linear replicons are terminated by covalently closed hairpin (hp) telomeres. Hairpin telomeres are formed from replicated intermediates by the telomere resolvase, ResT, in a phosphoryl tra...

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Autores principales: Huang, Shu Hui, Cozart, McKayla R., Hart, Madison A., Kobryn, Kerri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388405/
https://www.ncbi.nlm.nih.gov/pubmed/28180323
http://dx.doi.org/10.1093/nar/gkw1243
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author Huang, Shu Hui
Cozart, McKayla R.
Hart, Madison A.
Kobryn, Kerri
author_facet Huang, Shu Hui
Cozart, McKayla R.
Hart, Madison A.
Kobryn, Kerri
author_sort Huang, Shu Hui
collection PubMed
description Spirochetes of the genus Borrelia possess unusual genomes harboring multiple linear and circular replicons. The linear replicons are terminated by covalently closed hairpin (hp) telomeres. Hairpin telomeres are formed from replicated intermediates by the telomere resolvase, ResT, in a phosphoryl transfer reaction with mechanistic similarities to those promoted by type 1B topoisomerases and tyrosine recombinases. There is growing evidence that ResT is multifunctional. Upon ResT depletion DNA replication unexpectedly ceases. Additionally, ResT possesses RecO-like biochemical activities being able to promote single-strand annealing on both free ssDNA and ssDNA complexed with cognate single-stranded DNA binding protein. We report here that ResT possesses DNA-dependent ATPase activity that promotes DNA unwinding with a 3΄-5΄ polarity. ResT can unwind a variety of substrates including synthetic replication forks and D-loops. We demonstrate that ResT's twin activities of DNA unwinding and annealing can drive regression of a model replication fork. These properties are similar to those of the RecQ helicase of the RecF pathway involved in DNA gap repair. We propose that ResT's combination of activities implicates it in replication and recombination processes operating on the linear chromosome and plasmids of Borrelia burgdorferi.
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spelling pubmed-53884052017-04-18 The Borrelia burgdorferi telomere resolvase, ResT, possesses ATP-dependent DNA unwinding activity Huang, Shu Hui Cozart, McKayla R. Hart, Madison A. Kobryn, Kerri Nucleic Acids Res Molecular Biology Spirochetes of the genus Borrelia possess unusual genomes harboring multiple linear and circular replicons. The linear replicons are terminated by covalently closed hairpin (hp) telomeres. Hairpin telomeres are formed from replicated intermediates by the telomere resolvase, ResT, in a phosphoryl transfer reaction with mechanistic similarities to those promoted by type 1B topoisomerases and tyrosine recombinases. There is growing evidence that ResT is multifunctional. Upon ResT depletion DNA replication unexpectedly ceases. Additionally, ResT possesses RecO-like biochemical activities being able to promote single-strand annealing on both free ssDNA and ssDNA complexed with cognate single-stranded DNA binding protein. We report here that ResT possesses DNA-dependent ATPase activity that promotes DNA unwinding with a 3΄-5΄ polarity. ResT can unwind a variety of substrates including synthetic replication forks and D-loops. We demonstrate that ResT's twin activities of DNA unwinding and annealing can drive regression of a model replication fork. These properties are similar to those of the RecQ helicase of the RecF pathway involved in DNA gap repair. We propose that ResT's combination of activities implicates it in replication and recombination processes operating on the linear chromosome and plasmids of Borrelia burgdorferi. Oxford University Press 2017-02-17 2016-12-09 /pmc/articles/PMC5388405/ /pubmed/28180323 http://dx.doi.org/10.1093/nar/gkw1243 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Molecular Biology
Huang, Shu Hui
Cozart, McKayla R.
Hart, Madison A.
Kobryn, Kerri
The Borrelia burgdorferi telomere resolvase, ResT, possesses ATP-dependent DNA unwinding activity
title The Borrelia burgdorferi telomere resolvase, ResT, possesses ATP-dependent DNA unwinding activity
title_full The Borrelia burgdorferi telomere resolvase, ResT, possesses ATP-dependent DNA unwinding activity
title_fullStr The Borrelia burgdorferi telomere resolvase, ResT, possesses ATP-dependent DNA unwinding activity
title_full_unstemmed The Borrelia burgdorferi telomere resolvase, ResT, possesses ATP-dependent DNA unwinding activity
title_short The Borrelia burgdorferi telomere resolvase, ResT, possesses ATP-dependent DNA unwinding activity
title_sort borrelia burgdorferi telomere resolvase, rest, possesses atp-dependent dna unwinding activity
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388405/
https://www.ncbi.nlm.nih.gov/pubmed/28180323
http://dx.doi.org/10.1093/nar/gkw1243
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