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Atomic force microscopy of DNA in solution and DNA modelling show that structural properties specify the eukaryotic replication initiation site
The replication origins (ORIs) of Schizosaccharomyces pombe, like those in most eukaryotes, are long chromosomal regions localized within A+T-rich domains. Although there is no consensus sequence, the interacting proteins are strongly conserved, suggesting that DNA structure is important for ORI fun...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175326/ https://www.ncbi.nlm.nih.gov/pubmed/17933778 http://dx.doi.org/10.1093/nar/gkm733 |
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author | Marilley, Monique Milani, Pascale Thimonier, Jean Rocca-Serra, José Baldacci, Giuseppe |
author_facet | Marilley, Monique Milani, Pascale Thimonier, Jean Rocca-Serra, José Baldacci, Giuseppe |
author_sort | Marilley, Monique |
collection | PubMed |
description | The replication origins (ORIs) of Schizosaccharomyces pombe, like those in most eukaryotes, are long chromosomal regions localized within A+T-rich domains. Although there is no consensus sequence, the interacting proteins are strongly conserved, suggesting that DNA structure is important for ORI function. We used atomic force microscopy in solution and DNA modelling to study the structural properties of the Spars1 origin. We show that this segment is the least stable of the surrounding DNA (9 kb), and contains regions of intrinsically bent elements (strongly curved and inherently supercoiled DNAs). The pORC-binding site co-maps with a superhelical DNA region, where the spatial arrangement of adenine/thymine stretches may provide the binding substrate. The replication initiation site (RIP) is located within a strongly curved DNA region. On pORC unwinding, this site shifts towards the apex of the curvature, thus potentiating DNA melting there. Our model is entirely consistent with the sequence variability, large size and A+T-richness of ORIs, and also accounts for the multistep nature of the initiation process, the specificity of pORC-binding site(s), and the specific location of RIP. We show that the particular DNA features and dynamic properties identified in Spars1 are present in other eukaryotic origins. |
format | Text |
id | pubmed-2175326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21753262008-01-07 Atomic force microscopy of DNA in solution and DNA modelling show that structural properties specify the eukaryotic replication initiation site Marilley, Monique Milani, Pascale Thimonier, Jean Rocca-Serra, José Baldacci, Giuseppe Nucleic Acids Res Structural Biology The replication origins (ORIs) of Schizosaccharomyces pombe, like those in most eukaryotes, are long chromosomal regions localized within A+T-rich domains. Although there is no consensus sequence, the interacting proteins are strongly conserved, suggesting that DNA structure is important for ORI function. We used atomic force microscopy in solution and DNA modelling to study the structural properties of the Spars1 origin. We show that this segment is the least stable of the surrounding DNA (9 kb), and contains regions of intrinsically bent elements (strongly curved and inherently supercoiled DNAs). The pORC-binding site co-maps with a superhelical DNA region, where the spatial arrangement of adenine/thymine stretches may provide the binding substrate. The replication initiation site (RIP) is located within a strongly curved DNA region. On pORC unwinding, this site shifts towards the apex of the curvature, thus potentiating DNA melting there. Our model is entirely consistent with the sequence variability, large size and A+T-richness of ORIs, and also accounts for the multistep nature of the initiation process, the specificity of pORC-binding site(s), and the specific location of RIP. We show that the particular DNA features and dynamic properties identified in Spars1 are present in other eukaryotic origins. Oxford University Press 2007-11 2007-10-11 /pmc/articles/PMC2175326/ /pubmed/17933778 http://dx.doi.org/10.1093/nar/gkm733 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Structural Biology Marilley, Monique Milani, Pascale Thimonier, Jean Rocca-Serra, José Baldacci, Giuseppe Atomic force microscopy of DNA in solution and DNA modelling show that structural properties specify the eukaryotic replication initiation site |
title | Atomic force microscopy of DNA in solution and DNA modelling show that structural properties specify the eukaryotic replication initiation site |
title_full | Atomic force microscopy of DNA in solution and DNA modelling show that structural properties specify the eukaryotic replication initiation site |
title_fullStr | Atomic force microscopy of DNA in solution and DNA modelling show that structural properties specify the eukaryotic replication initiation site |
title_full_unstemmed | Atomic force microscopy of DNA in solution and DNA modelling show that structural properties specify the eukaryotic replication initiation site |
title_short | Atomic force microscopy of DNA in solution and DNA modelling show that structural properties specify the eukaryotic replication initiation site |
title_sort | atomic force microscopy of dna in solution and dna modelling show that structural properties specify the eukaryotic replication initiation site |
topic | Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175326/ https://www.ncbi.nlm.nih.gov/pubmed/17933778 http://dx.doi.org/10.1093/nar/gkm733 |
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