Chromatin dynamics during interphase explored by single-particle tracking

Our view of the structure and function of the interphase nucleus has changed drastically in recent years. It is now widely accepted that the nucleus is a well organized and highly compartmentalized organelle and that this organization is intimately related to nuclear function. In this context, chrom...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Levi, V., Gratton, E.
Formato: Artículo publishedVersion
Lenguaje:Inglés
Publicado: 2008
Materias:
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_09673849_v16_n3_p439_Levi
Aporte de:
id paperaa:paper_09673849_v16_n3_p439_Levi
record_format dspace
spelling paperaa:paper_09673849_v16_n3_p439_Levi2023-06-12T16:48:48Z Chromatin dynamics during interphase explored by single-particle tracking Chromosome Res. 2008;16(3):439-449 Levi, V. Gratton, E. Chromatin dynamics Single-particle tracking Two-photon microscopy green fluorescent protein polymer repressor protein cell nucleus chromatin gene control gene locus genetic organization human interphase nonhuman operator gene photon priority journal review Animals CHO Cells Chromatin Cricetinae Cricetulus Green Fluorescent Proteins Interphase Microscopy, Fluorescence, Multiphoton Recombinant Proteins Bacteria (microorganisms) Our view of the structure and function of the interphase nucleus has changed drastically in recent years. It is now widely accepted that the nucleus is a well organized and highly compartmentalized organelle and that this organization is intimately related to nuclear function. In this context, chromatin-initially considered a randomly entangled polymer-has also been shown to be structurally organized in interphase and its organization was found to be very important to gene regulation. Relevant and not completely answered questions are how chromatin organization is achieved and what mechanisms are responsible for changes in the positions of chromatin loci in the nucleus. A significant advance in the field resulted from tagging chromosome sites with bacterial operator sequences, and visualizing these tags using green fluorescent protein fused with the appropriate repressor protein. Simultaneously, fluorescence imaging techniques evolved significantly during recent years, allowing observation of the time evolution of processes in living specimens. In this context, the motion of the tagged locus was observed and analyzed to extract quantitative information regarding its dynamics. This review focuses on recent advances in our understanding of chromatin dynamics in interphase with the emphasis placed on the information obtained from single-particle tracking (SPT) experiments. We introduce the basis of SPT methods and trajectory analysis, and summarize what has been learnt by using this new technology in the context of chromatin dynamics. Finally, we briefly describe a method of SPT in a two-photon excitation microscope that has several advantages over methods based on conventional microscopy and review the information obtained using this novel approach to study chromatin dynamics. © 2008 Springer. Fil:Levi, V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2008 info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion application/pdf eng info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_09673849_v16_n3_p439_Levi
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
language Inglés
orig_language_str_mv eng
topic Chromatin dynamics
Single-particle tracking
Two-photon microscopy
green fluorescent protein
polymer
repressor protein
cell nucleus
chromatin
gene control
gene locus
genetic organization
human
interphase
nonhuman
operator gene
photon
priority journal
review
Animals
CHO Cells
Chromatin
Cricetinae
Cricetulus
Green Fluorescent Proteins
Interphase
Microscopy, Fluorescence, Multiphoton
Recombinant Proteins
Bacteria (microorganisms)
spellingShingle Chromatin dynamics
Single-particle tracking
Two-photon microscopy
green fluorescent protein
polymer
repressor protein
cell nucleus
chromatin
gene control
gene locus
genetic organization
human
interphase
nonhuman
operator gene
photon
priority journal
review
Animals
CHO Cells
Chromatin
Cricetinae
Cricetulus
Green Fluorescent Proteins
Interphase
Microscopy, Fluorescence, Multiphoton
Recombinant Proteins
Bacteria (microorganisms)
Levi, V.
Gratton, E.
Chromatin dynamics during interphase explored by single-particle tracking
topic_facet Chromatin dynamics
Single-particle tracking
Two-photon microscopy
green fluorescent protein
polymer
repressor protein
cell nucleus
chromatin
gene control
gene locus
genetic organization
human
interphase
nonhuman
operator gene
photon
priority journal
review
Animals
CHO Cells
Chromatin
Cricetinae
Cricetulus
Green Fluorescent Proteins
Interphase
Microscopy, Fluorescence, Multiphoton
Recombinant Proteins
Bacteria (microorganisms)
description Our view of the structure and function of the interphase nucleus has changed drastically in recent years. It is now widely accepted that the nucleus is a well organized and highly compartmentalized organelle and that this organization is intimately related to nuclear function. In this context, chromatin-initially considered a randomly entangled polymer-has also been shown to be structurally organized in interphase and its organization was found to be very important to gene regulation. Relevant and not completely answered questions are how chromatin organization is achieved and what mechanisms are responsible for changes in the positions of chromatin loci in the nucleus. A significant advance in the field resulted from tagging chromosome sites with bacterial operator sequences, and visualizing these tags using green fluorescent protein fused with the appropriate repressor protein. Simultaneously, fluorescence imaging techniques evolved significantly during recent years, allowing observation of the time evolution of processes in living specimens. In this context, the motion of the tagged locus was observed and analyzed to extract quantitative information regarding its dynamics. This review focuses on recent advances in our understanding of chromatin dynamics in interphase with the emphasis placed on the information obtained from single-particle tracking (SPT) experiments. We introduce the basis of SPT methods and trajectory analysis, and summarize what has been learnt by using this new technology in the context of chromatin dynamics. Finally, we briefly describe a method of SPT in a two-photon excitation microscope that has several advantages over methods based on conventional microscopy and review the information obtained using this novel approach to study chromatin dynamics. © 2008 Springer.
format Artículo
Artículo
publishedVersion
author Levi, V.
Gratton, E.
author_facet Levi, V.
Gratton, E.
author_sort Levi, V.
title Chromatin dynamics during interphase explored by single-particle tracking
title_short Chromatin dynamics during interphase explored by single-particle tracking
title_full Chromatin dynamics during interphase explored by single-particle tracking
title_fullStr Chromatin dynamics during interphase explored by single-particle tracking
title_full_unstemmed Chromatin dynamics during interphase explored by single-particle tracking
title_sort chromatin dynamics during interphase explored by single-particle tracking
publishDate 2008
url http://hdl.handle.net/20.500.12110/paper_09673849_v16_n3_p439_Levi
work_keys_str_mv AT leviv chromatindynamicsduringinterphaseexploredbysingleparticletracking
AT grattone chromatindynamicsduringinterphaseexploredbysingleparticletracking
_version_ 1769810035977748480