Cargando…

Direct quantification of the translocation activities of Saccharomyces cerevisiae Pif1 helicase

Saccharomyces cerevisiae Pif1 (ScPif1) is known as an ATP-dependent DNA helicase that plays critical roles in a number of important biological processes such as DNA replication, telomere maintenance and genome stability maintenance. Besides its DNA helicase activity, ScPif1 is also known as a single...

Descripción completa

Detalles Bibliográficos
Autores principales: Lu, Chen, Le, Shimin, Chen, Jin, Byrd, Alicia K, Rhodes, Daniela, Raney, Kevin D, Yan, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698741/
https://www.ncbi.nlm.nih.gov/pubmed/31216020
http://dx.doi.org/10.1093/nar/gkz541
_version_ 1783444605723738112
author Lu, Chen
Le, Shimin
Chen, Jin
Byrd, Alicia K
Rhodes, Daniela
Raney, Kevin D
Yan, Jie
author_facet Lu, Chen
Le, Shimin
Chen, Jin
Byrd, Alicia K
Rhodes, Daniela
Raney, Kevin D
Yan, Jie
author_sort Lu, Chen
collection PubMed
description Saccharomyces cerevisiae Pif1 (ScPif1) is known as an ATP-dependent DNA helicase that plays critical roles in a number of important biological processes such as DNA replication, telomere maintenance and genome stability maintenance. Besides its DNA helicase activity, ScPif1 is also known as a single-stranded DNA (ssDNA) translocase, while how ScPif1 translocates on ssDNA is unclear. Here, by measuring the translocation activity of individual ScPif1 molecules on ssDNA extended by mechanical force, we identified two distinct types of ssDNA translocation. In one type, ScPif1 moves along the ssDNA track with a rate of ∼140 nt/s in 100 μM ATP, whereas in the other type, ScPif1 is immobilized to a fixed location of ssDNA and generates ssDNA loops against force. Between the two, the mobile translocation is the major form at nanomolar ScPif1 concentrations although patrolling becomes more frequent at micromolar concentrations. Together, our results suggest that ScPif1 translocates on extended ssDNA in two distinct modes, primarily in a ‘mobile’ manner.
format Online
Article
Text
id pubmed-6698741
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-66987412019-08-22 Direct quantification of the translocation activities of Saccharomyces cerevisiae Pif1 helicase Lu, Chen Le, Shimin Chen, Jin Byrd, Alicia K Rhodes, Daniela Raney, Kevin D Yan, Jie Nucleic Acids Res Molecular Biology Saccharomyces cerevisiae Pif1 (ScPif1) is known as an ATP-dependent DNA helicase that plays critical roles in a number of important biological processes such as DNA replication, telomere maintenance and genome stability maintenance. Besides its DNA helicase activity, ScPif1 is also known as a single-stranded DNA (ssDNA) translocase, while how ScPif1 translocates on ssDNA is unclear. Here, by measuring the translocation activity of individual ScPif1 molecules on ssDNA extended by mechanical force, we identified two distinct types of ssDNA translocation. In one type, ScPif1 moves along the ssDNA track with a rate of ∼140 nt/s in 100 μM ATP, whereas in the other type, ScPif1 is immobilized to a fixed location of ssDNA and generates ssDNA loops against force. Between the two, the mobile translocation is the major form at nanomolar ScPif1 concentrations although patrolling becomes more frequent at micromolar concentrations. Together, our results suggest that ScPif1 translocates on extended ssDNA in two distinct modes, primarily in a ‘mobile’ manner. Oxford University Press 2019-08-22 2019-06-19 /pmc/articles/PMC6698741/ /pubmed/31216020 http://dx.doi.org/10.1093/nar/gkz541 Text en © The Author(s) 2019. 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 Non-Commercial 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
Lu, Chen
Le, Shimin
Chen, Jin
Byrd, Alicia K
Rhodes, Daniela
Raney, Kevin D
Yan, Jie
Direct quantification of the translocation activities of Saccharomyces cerevisiae Pif1 helicase
title Direct quantification of the translocation activities of Saccharomyces cerevisiae Pif1 helicase
title_full Direct quantification of the translocation activities of Saccharomyces cerevisiae Pif1 helicase
title_fullStr Direct quantification of the translocation activities of Saccharomyces cerevisiae Pif1 helicase
title_full_unstemmed Direct quantification of the translocation activities of Saccharomyces cerevisiae Pif1 helicase
title_short Direct quantification of the translocation activities of Saccharomyces cerevisiae Pif1 helicase
title_sort direct quantification of the translocation activities of saccharomyces cerevisiae pif1 helicase
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698741/
https://www.ncbi.nlm.nih.gov/pubmed/31216020
http://dx.doi.org/10.1093/nar/gkz541
work_keys_str_mv AT luchen directquantificationofthetranslocationactivitiesofsaccharomycescerevisiaepif1helicase
AT leshimin directquantificationofthetranslocationactivitiesofsaccharomycescerevisiaepif1helicase
AT chenjin directquantificationofthetranslocationactivitiesofsaccharomycescerevisiaepif1helicase
AT byrdaliciak directquantificationofthetranslocationactivitiesofsaccharomycescerevisiaepif1helicase
AT rhodesdaniela directquantificationofthetranslocationactivitiesofsaccharomycescerevisiaepif1helicase
AT raneykevind directquantificationofthetranslocationactivitiesofsaccharomycescerevisiaepif1helicase
AT yanjie directquantificationofthetranslocationactivitiesofsaccharomycescerevisiaepif1helicase