The lighthouse at the end of the chromosome* [version 1; referees: 3 approved]

Fluorescence microscopy can be used to assess the dynamic localization and intensity of single entities in vitro or in living cells. It has been applied with aplomb to many different cellular processes and has significantly enlightened our understanding of the heterogeneity and complexity of biologi...

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Main Authors: Yahya Benslimane, Lea Harrington
Format: Article
Language:English
Published: F1000 Research Ltd 2015-12-01
Series:F1000Research
Subjects:
Online Access:http://f1000research.com/articles/4-1427/v1
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spelling doaj-2b79a7b1899a4044a91770fc13b338482020-11-25T02:54:40ZengF1000 Research LtdF1000Research2046-14022015-12-01410.12688/f1000research.6664.17160The lighthouse at the end of the chromosome* [version 1; referees: 3 approved]Yahya Benslimane0Lea Harrington1Department of Molecular Biology, University of Montreal, Institute for Research in Immunology and Cancer, Montreal, Quebec, CanadaDepartment of Medicine, University of Montreal, Institute for Research in Immunology and Cancer, Montreal, Quebec, CanadaFluorescence microscopy can be used to assess the dynamic localization and intensity of single entities in vitro or in living cells. It has been applied with aplomb to many different cellular processes and has significantly enlightened our understanding of the heterogeneity and complexity of biological systems. Recently, high-resolution fluorescence microscopy has been brought to bear on telomeres, leading to new insights into telomere spatial organization and accessibility, and into the mechanistic nuances of telomere elongation. We provide a snapshot of some of these recent advances with a focus on mammalian systems, and show how three-dimensional, time-lapse microscopy and single-molecule fluorescence shine a new light on the end of the chromosome.http://f1000research.com/articles/4-1427/v1Experimental Biophysical MethodsNuclear Structure & FunctionProtein FoldingStructure: Transcription & Translation
collection DOAJ
language English
format Article
sources DOAJ
author Yahya Benslimane
Lea Harrington
spellingShingle Yahya Benslimane
Lea Harrington
The lighthouse at the end of the chromosome* [version 1; referees: 3 approved]
F1000Research
Experimental Biophysical Methods
Nuclear Structure & Function
Protein Folding
Structure: Transcription & Translation
author_facet Yahya Benslimane
Lea Harrington
author_sort Yahya Benslimane
title The lighthouse at the end of the chromosome* [version 1; referees: 3 approved]
title_short The lighthouse at the end of the chromosome* [version 1; referees: 3 approved]
title_full The lighthouse at the end of the chromosome* [version 1; referees: 3 approved]
title_fullStr The lighthouse at the end of the chromosome* [version 1; referees: 3 approved]
title_full_unstemmed The lighthouse at the end of the chromosome* [version 1; referees: 3 approved]
title_sort lighthouse at the end of the chromosome* [version 1; referees: 3 approved]
publisher F1000 Research Ltd
series F1000Research
issn 2046-1402
publishDate 2015-12-01
description Fluorescence microscopy can be used to assess the dynamic localization and intensity of single entities in vitro or in living cells. It has been applied with aplomb to many different cellular processes and has significantly enlightened our understanding of the heterogeneity and complexity of biological systems. Recently, high-resolution fluorescence microscopy has been brought to bear on telomeres, leading to new insights into telomere spatial organization and accessibility, and into the mechanistic nuances of telomere elongation. We provide a snapshot of some of these recent advances with a focus on mammalian systems, and show how three-dimensional, time-lapse microscopy and single-molecule fluorescence shine a new light on the end of the chromosome.
topic Experimental Biophysical Methods
Nuclear Structure & Function
Protein Folding
Structure: Transcription & Translation
url http://f1000research.com/articles/4-1427/v1
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