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Archaeal Hel308 suppresses recombination through a catalytic switch that controls DNA annealing

Hel308 helicases promote genome stability in archaea and are conserved in metazoans, where they are known as HELQ. Their helicase mechanism is well characterised, but it is unclear how they specifically contribute to genome stability in archaea. We show here that a highly conserved motif of Hel308/H...

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Autores principales: Lever, Rebecca J, Simmons, Emily, Gamble-Milner, Rebecca, Buckley, Ryan J, Harrison, Catherine, Parkes, Ashley J, Mitchell, Laura, Gausden, Jacob A, Škulj, Sanja, Bertoša, Branimir, Bolt, Edward L, Allers, Thorsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484726/
https://www.ncbi.nlm.nih.gov/pubmed/37409572
http://dx.doi.org/10.1093/nar/gkad572
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author Lever, Rebecca J
Simmons, Emily
Gamble-Milner, Rebecca
Buckley, Ryan J
Harrison, Catherine
Parkes, Ashley J
Mitchell, Laura
Gausden, Jacob A
Škulj, Sanja
Bertoša, Branimir
Bolt, Edward L
Allers, Thorsten
author_facet Lever, Rebecca J
Simmons, Emily
Gamble-Milner, Rebecca
Buckley, Ryan J
Harrison, Catherine
Parkes, Ashley J
Mitchell, Laura
Gausden, Jacob A
Škulj, Sanja
Bertoša, Branimir
Bolt, Edward L
Allers, Thorsten
author_sort Lever, Rebecca J
collection PubMed
description Hel308 helicases promote genome stability in archaea and are conserved in metazoans, where they are known as HELQ. Their helicase mechanism is well characterised, but it is unclear how they specifically contribute to genome stability in archaea. We show here that a highly conserved motif of Hel308/HELQ helicases (motif IVa, F/YHHAGL) modulates both DNA unwinding and a newly identified strand annealing function of archaeal Hel308. A single amino acid substitution in motif IVa results in hyper-active DNA helicase and annealase activities of purified Hel308 in vitro. All-atom molecular dynamics simulations using Hel308 crystal structures provided a molecular basis for these differences between mutant and wild type Hel308. In archaeal cells, the same mutation results in 160000-fold increased recombination, exclusively as gene conversion (non-crossover) events. However, crossover recombination is unaffected by the motif IVa mutation, as is cell viability or DNA damage sensitivity. By contrast, cells lacking Hel308 show impaired growth, increased sensitivity to DNA cross-linking agents, and only moderately increased recombination. Our data reveal that archaeal Hel308 suppresses recombination and promotes DNA repair, and that motif IVa in the RecA2 domain acts as a catalytic switch to modulate the separable recombination and repair activities of Hel308.
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spelling pubmed-104847262023-09-09 Archaeal Hel308 suppresses recombination through a catalytic switch that controls DNA annealing Lever, Rebecca J Simmons, Emily Gamble-Milner, Rebecca Buckley, Ryan J Harrison, Catherine Parkes, Ashley J Mitchell, Laura Gausden, Jacob A Škulj, Sanja Bertoša, Branimir Bolt, Edward L Allers, Thorsten Nucleic Acids Res Genome Integrity, Repair and Replication Hel308 helicases promote genome stability in archaea and are conserved in metazoans, where they are known as HELQ. Their helicase mechanism is well characterised, but it is unclear how they specifically contribute to genome stability in archaea. We show here that a highly conserved motif of Hel308/HELQ helicases (motif IVa, F/YHHAGL) modulates both DNA unwinding and a newly identified strand annealing function of archaeal Hel308. A single amino acid substitution in motif IVa results in hyper-active DNA helicase and annealase activities of purified Hel308 in vitro. All-atom molecular dynamics simulations using Hel308 crystal structures provided a molecular basis for these differences between mutant and wild type Hel308. In archaeal cells, the same mutation results in 160000-fold increased recombination, exclusively as gene conversion (non-crossover) events. However, crossover recombination is unaffected by the motif IVa mutation, as is cell viability or DNA damage sensitivity. By contrast, cells lacking Hel308 show impaired growth, increased sensitivity to DNA cross-linking agents, and only moderately increased recombination. Our data reveal that archaeal Hel308 suppresses recombination and promotes DNA repair, and that motif IVa in the RecA2 domain acts as a catalytic switch to modulate the separable recombination and repair activities of Hel308. Oxford University Press 2023-07-06 /pmc/articles/PMC10484726/ /pubmed/37409572 http://dx.doi.org/10.1093/nar/gkad572 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genome Integrity, Repair and Replication
Lever, Rebecca J
Simmons, Emily
Gamble-Milner, Rebecca
Buckley, Ryan J
Harrison, Catherine
Parkes, Ashley J
Mitchell, Laura
Gausden, Jacob A
Škulj, Sanja
Bertoša, Branimir
Bolt, Edward L
Allers, Thorsten
Archaeal Hel308 suppresses recombination through a catalytic switch that controls DNA annealing
title Archaeal Hel308 suppresses recombination through a catalytic switch that controls DNA annealing
title_full Archaeal Hel308 suppresses recombination through a catalytic switch that controls DNA annealing
title_fullStr Archaeal Hel308 suppresses recombination through a catalytic switch that controls DNA annealing
title_full_unstemmed Archaeal Hel308 suppresses recombination through a catalytic switch that controls DNA annealing
title_short Archaeal Hel308 suppresses recombination through a catalytic switch that controls DNA annealing
title_sort archaeal hel308 suppresses recombination through a catalytic switch that controls dna annealing
topic Genome Integrity, Repair and Replication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484726/
https://www.ncbi.nlm.nih.gov/pubmed/37409572
http://dx.doi.org/10.1093/nar/gkad572
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