Cargando…

High-temperature single-molecule kinetic analysis of thermophilic archaeal MCM helicases

The minichromosome maintenance (MCM) complex is the replicative helicase responsible for unwinding DNA during archaeal and eukaryal genome replication. To mimic long helicase events in the cell, a high-temperature single-molecule assay was designed to quantitatively measure long-range DNA unwinding...

Descripción completa

Detalles Bibliográficos
Autores principales: Schermerhorn, Kelly M., Tanner, Nathan, Kelman, Zvi, Gardner, Andrew F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062978/
https://www.ncbi.nlm.nih.gov/pubmed/27382065
http://dx.doi.org/10.1093/nar/gkw612
_version_ 1782459888151035904
author Schermerhorn, Kelly M.
Tanner, Nathan
Kelman, Zvi
Gardner, Andrew F.
author_facet Schermerhorn, Kelly M.
Tanner, Nathan
Kelman, Zvi
Gardner, Andrew F.
author_sort Schermerhorn, Kelly M.
collection PubMed
description The minichromosome maintenance (MCM) complex is the replicative helicase responsible for unwinding DNA during archaeal and eukaryal genome replication. To mimic long helicase events in the cell, a high-temperature single-molecule assay was designed to quantitatively measure long-range DNA unwinding of individual DNA helicases from the archaeons Methanothermobacter thermautotrophicus (Mth) and Thermococcus sp. 9°N (9°N). Mth encodes a single MCM homolog while 9°N encodes three helicases. 9°N MCM3, the proposed replicative helicase, unwinds DNA at a faster rate compared to 9°N MCM2 and to Mth MCM. However, all three MCM proteins have similar processivities. The implications of these observations for DNA replication in archaea and the differences and similarities among helicases from different microorganisms are discussed. Development of the high-temperature single-molecule assay establishes a system to comprehensively study thermophilic replisomes and evolutionary links between archaeal, eukaryal, and bacterial replication systems.
format Online
Article
Text
id pubmed-5062978
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-50629782016-10-14 High-temperature single-molecule kinetic analysis of thermophilic archaeal MCM helicases Schermerhorn, Kelly M. Tanner, Nathan Kelman, Zvi Gardner, Andrew F. Nucleic Acids Res Genome Integrity, Repair and Replication The minichromosome maintenance (MCM) complex is the replicative helicase responsible for unwinding DNA during archaeal and eukaryal genome replication. To mimic long helicase events in the cell, a high-temperature single-molecule assay was designed to quantitatively measure long-range DNA unwinding of individual DNA helicases from the archaeons Methanothermobacter thermautotrophicus (Mth) and Thermococcus sp. 9°N (9°N). Mth encodes a single MCM homolog while 9°N encodes three helicases. 9°N MCM3, the proposed replicative helicase, unwinds DNA at a faster rate compared to 9°N MCM2 and to Mth MCM. However, all three MCM proteins have similar processivities. The implications of these observations for DNA replication in archaea and the differences and similarities among helicases from different microorganisms are discussed. Development of the high-temperature single-molecule assay establishes a system to comprehensively study thermophilic replisomes and evolutionary links between archaeal, eukaryal, and bacterial replication systems. Oxford University Press 2016-10-14 2016-07-05 /pmc/articles/PMC5062978/ /pubmed/27382065 http://dx.doi.org/10.1093/nar/gkw612 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 Genome Integrity, Repair and Replication
Schermerhorn, Kelly M.
Tanner, Nathan
Kelman, Zvi
Gardner, Andrew F.
High-temperature single-molecule kinetic analysis of thermophilic archaeal MCM helicases
title High-temperature single-molecule kinetic analysis of thermophilic archaeal MCM helicases
title_full High-temperature single-molecule kinetic analysis of thermophilic archaeal MCM helicases
title_fullStr High-temperature single-molecule kinetic analysis of thermophilic archaeal MCM helicases
title_full_unstemmed High-temperature single-molecule kinetic analysis of thermophilic archaeal MCM helicases
title_short High-temperature single-molecule kinetic analysis of thermophilic archaeal MCM helicases
title_sort high-temperature single-molecule kinetic analysis of thermophilic archaeal mcm helicases
topic Genome Integrity, Repair and Replication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062978/
https://www.ncbi.nlm.nih.gov/pubmed/27382065
http://dx.doi.org/10.1093/nar/gkw612
work_keys_str_mv AT schermerhornkellym hightemperaturesinglemoleculekineticanalysisofthermophilicarchaealmcmhelicases
AT tannernathan hightemperaturesinglemoleculekineticanalysisofthermophilicarchaealmcmhelicases
AT kelmanzvi hightemperaturesinglemoleculekineticanalysisofthermophilicarchaealmcmhelicases
AT gardnerandrewf hightemperaturesinglemoleculekineticanalysisofthermophilicarchaealmcmhelicases