Cargando…
Measurement of replication structures at the nanometer scale using super-resolution light microscopy
DNA replication, similar to other cellular processes, occurs within dynamic macromolecular structures. Any comprehensive understanding ultimately requires quantitative data to establish and test models of genome duplication. We used two different super-resolution light microscopy techniques to direc...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811013/ https://www.ncbi.nlm.nih.gov/pubmed/19864256 http://dx.doi.org/10.1093/nar/gkp901 |
_version_ | 1782176719335063552 |
---|---|
author | Baddeley, D. Chagin, V. O. Schermelleh, L. Martin, S. Pombo, A. Carlton, P. M. Gahl, A. Domaing, P. Birk, U. Leonhardt, H. Cremer, C. Cardoso, M. C. |
author_facet | Baddeley, D. Chagin, V. O. Schermelleh, L. Martin, S. Pombo, A. Carlton, P. M. Gahl, A. Domaing, P. Birk, U. Leonhardt, H. Cremer, C. Cardoso, M. C. |
author_sort | Baddeley, D. |
collection | PubMed |
description | DNA replication, similar to other cellular processes, occurs within dynamic macromolecular structures. Any comprehensive understanding ultimately requires quantitative data to establish and test models of genome duplication. We used two different super-resolution light microscopy techniques to directly measure and compare the size and numbers of replication foci in mammalian cells. This analysis showed that replication foci vary in size from 210 nm down to 40 nm. Remarkably, spatially modulated illumination (SMI) and 3D-structured illumination microscopy (3D-SIM) both showed an average size of 125 nm that was conserved throughout S-phase and independent of the labeling method, suggesting a basic unit of genome duplication. Interestingly, the improved optical 3D resolution identified 3- to 5-fold more distinct replication foci than previously reported. These results show that optical nanoscopy techniques enable accurate measurements of cellular structures at a level previously achieved only by electron microscopy and highlight the possibility of high-throughput, multispectral 3D analyses. |
format | Text |
id | pubmed-2811013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28110132010-01-26 Measurement of replication structures at the nanometer scale using super-resolution light microscopy Baddeley, D. Chagin, V. O. Schermelleh, L. Martin, S. Pombo, A. Carlton, P. M. Gahl, A. Domaing, P. Birk, U. Leonhardt, H. Cremer, C. Cardoso, M. C. Nucleic Acids Res Methods Online DNA replication, similar to other cellular processes, occurs within dynamic macromolecular structures. Any comprehensive understanding ultimately requires quantitative data to establish and test models of genome duplication. We used two different super-resolution light microscopy techniques to directly measure and compare the size and numbers of replication foci in mammalian cells. This analysis showed that replication foci vary in size from 210 nm down to 40 nm. Remarkably, spatially modulated illumination (SMI) and 3D-structured illumination microscopy (3D-SIM) both showed an average size of 125 nm that was conserved throughout S-phase and independent of the labeling method, suggesting a basic unit of genome duplication. Interestingly, the improved optical 3D resolution identified 3- to 5-fold more distinct replication foci than previously reported. These results show that optical nanoscopy techniques enable accurate measurements of cellular structures at a level previously achieved only by electron microscopy and highlight the possibility of high-throughput, multispectral 3D analyses. Oxford University Press 2010-01 2009-10-28 /pmc/articles/PMC2811013/ /pubmed/19864256 http://dx.doi.org/10.1093/nar/gkp901 Text en © The Author(s) 2009. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5/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/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Baddeley, D. Chagin, V. O. Schermelleh, L. Martin, S. Pombo, A. Carlton, P. M. Gahl, A. Domaing, P. Birk, U. Leonhardt, H. Cremer, C. Cardoso, M. C. Measurement of replication structures at the nanometer scale using super-resolution light microscopy |
title | Measurement of replication structures at the nanometer scale using super-resolution light microscopy |
title_full | Measurement of replication structures at the nanometer scale using super-resolution light microscopy |
title_fullStr | Measurement of replication structures at the nanometer scale using super-resolution light microscopy |
title_full_unstemmed | Measurement of replication structures at the nanometer scale using super-resolution light microscopy |
title_short | Measurement of replication structures at the nanometer scale using super-resolution light microscopy |
title_sort | measurement of replication structures at the nanometer scale using super-resolution light microscopy |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811013/ https://www.ncbi.nlm.nih.gov/pubmed/19864256 http://dx.doi.org/10.1093/nar/gkp901 |
work_keys_str_mv | AT baddeleyd measurementofreplicationstructuresatthenanometerscaleusingsuperresolutionlightmicroscopy AT chaginvo measurementofreplicationstructuresatthenanometerscaleusingsuperresolutionlightmicroscopy AT schermellehl measurementofreplicationstructuresatthenanometerscaleusingsuperresolutionlightmicroscopy AT martins measurementofreplicationstructuresatthenanometerscaleusingsuperresolutionlightmicroscopy AT pomboa measurementofreplicationstructuresatthenanometerscaleusingsuperresolutionlightmicroscopy AT carltonpm measurementofreplicationstructuresatthenanometerscaleusingsuperresolutionlightmicroscopy AT gahla measurementofreplicationstructuresatthenanometerscaleusingsuperresolutionlightmicroscopy AT domaingp measurementofreplicationstructuresatthenanometerscaleusingsuperresolutionlightmicroscopy AT birku measurementofreplicationstructuresatthenanometerscaleusingsuperresolutionlightmicroscopy AT leonhardth measurementofreplicationstructuresatthenanometerscaleusingsuperresolutionlightmicroscopy AT cremerc measurementofreplicationstructuresatthenanometerscaleusingsuperresolutionlightmicroscopy AT cardosomc measurementofreplicationstructuresatthenanometerscaleusingsuperresolutionlightmicroscopy |