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Advanced fluorescence microscopy methods for the real-time study of transcription and chromatin dynamics

In this contribution we provide an overview of the recent advances allowed by the use of fluorescence microscopy methods in the study of transcriptional processes and their interplay with the chromatin architecture in living cells. Although the use of fluorophores to label nucleic acids dates back a...

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Detalles Bibliográficos
Autores principales: Annibale, Paolo, Gratton, Enrico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214231/
https://www.ncbi.nlm.nih.gov/pubmed/25764219
http://dx.doi.org/10.4161/trns.28425
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author Annibale, Paolo
Gratton, Enrico
author_facet Annibale, Paolo
Gratton, Enrico
author_sort Annibale, Paolo
collection PubMed
description In this contribution we provide an overview of the recent advances allowed by the use of fluorescence microscopy methods in the study of transcriptional processes and their interplay with the chromatin architecture in living cells. Although the use of fluorophores to label nucleic acids dates back at least to about half a century ago,(1) two recent breakthroughs have effectively opened the way to use fluorescence routinely for specific and quantitative probing of chromatin organization and transcriptional activity in living cells: namely, the possibility of labeling first the chromatin loci and then the mRNA synthesized from a gene using fluorescent proteins. In this contribution we focus on methods that can probe rapid dynamic processes by analyzing fast fluorescence fluctuations.
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spelling pubmed-42142312015-09-27 Advanced fluorescence microscopy methods for the real-time study of transcription and chromatin dynamics Annibale, Paolo Gratton, Enrico Transcription Review In this contribution we provide an overview of the recent advances allowed by the use of fluorescence microscopy methods in the study of transcriptional processes and their interplay with the chromatin architecture in living cells. Although the use of fluorophores to label nucleic acids dates back at least to about half a century ago,(1) two recent breakthroughs have effectively opened the way to use fluorescence routinely for specific and quantitative probing of chromatin organization and transcriptional activity in living cells: namely, the possibility of labeling first the chromatin loci and then the mRNA synthesized from a gene using fluorescent proteins. In this contribution we focus on methods that can probe rapid dynamic processes by analyzing fast fluorescence fluctuations. Landes Bioscience 2014-03-12 /pmc/articles/PMC4214231/ /pubmed/25764219 http://dx.doi.org/10.4161/trns.28425 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
Annibale, Paolo
Gratton, Enrico
Advanced fluorescence microscopy methods for the real-time study of transcription and chromatin dynamics
title Advanced fluorescence microscopy methods for the real-time study of transcription and chromatin dynamics
title_full Advanced fluorescence microscopy methods for the real-time study of transcription and chromatin dynamics
title_fullStr Advanced fluorescence microscopy methods for the real-time study of transcription and chromatin dynamics
title_full_unstemmed Advanced fluorescence microscopy methods for the real-time study of transcription and chromatin dynamics
title_short Advanced fluorescence microscopy methods for the real-time study of transcription and chromatin dynamics
title_sort advanced fluorescence microscopy methods for the real-time study of transcription and chromatin dynamics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214231/
https://www.ncbi.nlm.nih.gov/pubmed/25764219
http://dx.doi.org/10.4161/trns.28425
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