Cargando…

DNA cleavage site selection by Type III restriction enzymes provides evidence for head-on protein collisions following 1D bidirectional motion

DNA cleavage by the Type III Restriction–Modification enzymes requires communication in 1D between two distant indirectly-repeated recognitions sites, yet results in non-specific dsDNA cleavage close to only one of the two sites. To test a recently proposed ATP-triggered DNA sliding model, we addres...

Descripción completa

Detalles Bibliográficos
Autores principales: Schwarz, Friedrich W., van Aelst, Kara, Tóth, Júlia, Seidel, Ralf, Szczelkun, Mark D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185417/
https://www.ncbi.nlm.nih.gov/pubmed/21724613
http://dx.doi.org/10.1093/nar/gkr502
_version_ 1782213209455853568
author Schwarz, Friedrich W.
van Aelst, Kara
Tóth, Júlia
Seidel, Ralf
Szczelkun, Mark D.
author_facet Schwarz, Friedrich W.
van Aelst, Kara
Tóth, Júlia
Seidel, Ralf
Szczelkun, Mark D.
author_sort Schwarz, Friedrich W.
collection PubMed
description DNA cleavage by the Type III Restriction–Modification enzymes requires communication in 1D between two distant indirectly-repeated recognitions sites, yet results in non-specific dsDNA cleavage close to only one of the two sites. To test a recently proposed ATP-triggered DNA sliding model, we addressed why one site is selected over another during cleavage. We examined the relative cleavage of a pair of identical sites on DNA substrates with different distances to a free or protein blocked end, and on a DNA substrate using different relative concentrations of protein. Under these conditions a bias can be induced in the cleavage of one site over the other. Monte-Carlo simulations based on the sliding model reproduce the experimentally observed behaviour. This suggests that cleavage site selection simply reflects the dynamics of the preceding stochastic enzyme events that are consistent with bidirectional motion in 1D and DNA cleavage following head-on protein collision.
format Online
Article
Text
id pubmed-3185417
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-31854172011-10-04 DNA cleavage site selection by Type III restriction enzymes provides evidence for head-on protein collisions following 1D bidirectional motion Schwarz, Friedrich W. van Aelst, Kara Tóth, Júlia Seidel, Ralf Szczelkun, Mark D. Nucleic Acids Res Nucleic Acid Enzymes DNA cleavage by the Type III Restriction–Modification enzymes requires communication in 1D between two distant indirectly-repeated recognitions sites, yet results in non-specific dsDNA cleavage close to only one of the two sites. To test a recently proposed ATP-triggered DNA sliding model, we addressed why one site is selected over another during cleavage. We examined the relative cleavage of a pair of identical sites on DNA substrates with different distances to a free or protein blocked end, and on a DNA substrate using different relative concentrations of protein. Under these conditions a bias can be induced in the cleavage of one site over the other. Monte-Carlo simulations based on the sliding model reproduce the experimentally observed behaviour. This suggests that cleavage site selection simply reflects the dynamics of the preceding stochastic enzyme events that are consistent with bidirectional motion in 1D and DNA cleavage following head-on protein collision. Oxford University Press 2011-10 2011-06-30 /pmc/articles/PMC3185417/ /pubmed/21724613 http://dx.doi.org/10.1093/nar/gkr502 Text en © The Author(s) 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Nucleic Acid Enzymes
Schwarz, Friedrich W.
van Aelst, Kara
Tóth, Júlia
Seidel, Ralf
Szczelkun, Mark D.
DNA cleavage site selection by Type III restriction enzymes provides evidence for head-on protein collisions following 1D bidirectional motion
title DNA cleavage site selection by Type III restriction enzymes provides evidence for head-on protein collisions following 1D bidirectional motion
title_full DNA cleavage site selection by Type III restriction enzymes provides evidence for head-on protein collisions following 1D bidirectional motion
title_fullStr DNA cleavage site selection by Type III restriction enzymes provides evidence for head-on protein collisions following 1D bidirectional motion
title_full_unstemmed DNA cleavage site selection by Type III restriction enzymes provides evidence for head-on protein collisions following 1D bidirectional motion
title_short DNA cleavage site selection by Type III restriction enzymes provides evidence for head-on protein collisions following 1D bidirectional motion
title_sort dna cleavage site selection by type iii restriction enzymes provides evidence for head-on protein collisions following 1d bidirectional motion
topic Nucleic Acid Enzymes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185417/
https://www.ncbi.nlm.nih.gov/pubmed/21724613
http://dx.doi.org/10.1093/nar/gkr502
work_keys_str_mv AT schwarzfriedrichw dnacleavagesiteselectionbytypeiiirestrictionenzymesprovidesevidenceforheadonproteincollisionsfollowing1dbidirectionalmotion
AT vanaelstkara dnacleavagesiteselectionbytypeiiirestrictionenzymesprovidesevidenceforheadonproteincollisionsfollowing1dbidirectionalmotion
AT tothjulia dnacleavagesiteselectionbytypeiiirestrictionenzymesprovidesevidenceforheadonproteincollisionsfollowing1dbidirectionalmotion
AT seidelralf dnacleavagesiteselectionbytypeiiirestrictionenzymesprovidesevidenceforheadonproteincollisionsfollowing1dbidirectionalmotion
AT szczelkunmarkd dnacleavagesiteselectionbytypeiiirestrictionenzymesprovidesevidenceforheadonproteincollisionsfollowing1dbidirectionalmotion