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Strength in numbers: quantitative single‐molecule RNA detection assays
Gene expression is a fundamental process that underlies development, homeostasis, and behavior of organisms. The fact that it relies on nucleic acid intermediates, which can specifically interact with complementary probes, provides an excellent opportunity for studying the multiple steps—transcripti...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5024021/ https://www.ncbi.nlm.nih.gov/pubmed/25645249 http://dx.doi.org/10.1002/wdev.170 |
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author | Gaspar, Imre Ephrussi, Anne |
author_facet | Gaspar, Imre Ephrussi, Anne |
author_sort | Gaspar, Imre |
collection | PubMed |
description | Gene expression is a fundamental process that underlies development, homeostasis, and behavior of organisms. The fact that it relies on nucleic acid intermediates, which can specifically interact with complementary probes, provides an excellent opportunity for studying the multiple steps—transcription, RNA processing, transport, translation, degradation, and so forth—through which gene function manifests. Over the past three decades, the toolbox of nucleic acid science has expanded tremendously, making high‐precision in situ detection of DNA and RNA possible. This has revealed that many—probably the vast majority of—transcripts are distributed within the cytoplasm or the nucleus in a nonrandom fashion. With the development of microscopy techniques we have learned not only about the qualitative localization of these molecules but also about their absolute numbers with great precision. Single‐molecule techniques for nucleic acid detection have been transforming our views of biology with elementary power: cells are not average members of their population but are highly distinct individuals with greatly and suddenly changing gene expression, and this behavior of theirs can be measured, modeled, and thus predicted and, finally, comprehended. WIREs Dev Biol 2015, 4:135–150. doi: 10.1002/wdev.170 For further resources related to this article, please visit the WIREs website. Conflict of interest: The authors have declared no conflicts of interest for this article. |
format | Online Article Text |
id | pubmed-5024021 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50240212016-09-23 Strength in numbers: quantitative single‐molecule RNA detection assays Gaspar, Imre Ephrussi, Anne Wiley Interdiscip Rev Dev Biol Advanced Reviews Gene expression is a fundamental process that underlies development, homeostasis, and behavior of organisms. The fact that it relies on nucleic acid intermediates, which can specifically interact with complementary probes, provides an excellent opportunity for studying the multiple steps—transcription, RNA processing, transport, translation, degradation, and so forth—through which gene function manifests. Over the past three decades, the toolbox of nucleic acid science has expanded tremendously, making high‐precision in situ detection of DNA and RNA possible. This has revealed that many—probably the vast majority of—transcripts are distributed within the cytoplasm or the nucleus in a nonrandom fashion. With the development of microscopy techniques we have learned not only about the qualitative localization of these molecules but also about their absolute numbers with great precision. Single‐molecule techniques for nucleic acid detection have been transforming our views of biology with elementary power: cells are not average members of their population but are highly distinct individuals with greatly and suddenly changing gene expression, and this behavior of theirs can be measured, modeled, and thus predicted and, finally, comprehended. WIREs Dev Biol 2015, 4:135–150. doi: 10.1002/wdev.170 For further resources related to this article, please visit the WIREs website. Conflict of interest: The authors have declared no conflicts of interest for this article. John Wiley & Sons, Inc. 2015-01-21 2015 /pmc/articles/PMC5024021/ /pubmed/25645249 http://dx.doi.org/10.1002/wdev.170 Text en © 2015 The Authors. WIREs Developmental Biology published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Advanced Reviews Gaspar, Imre Ephrussi, Anne Strength in numbers: quantitative single‐molecule RNA detection assays |
title | Strength in numbers: quantitative single‐molecule RNA detection assays |
title_full | Strength in numbers: quantitative single‐molecule RNA detection assays |
title_fullStr | Strength in numbers: quantitative single‐molecule RNA detection assays |
title_full_unstemmed | Strength in numbers: quantitative single‐molecule RNA detection assays |
title_short | Strength in numbers: quantitative single‐molecule RNA detection assays |
title_sort | strength in numbers: quantitative single‐molecule rna detection assays |
topic | Advanced Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5024021/ https://www.ncbi.nlm.nih.gov/pubmed/25645249 http://dx.doi.org/10.1002/wdev.170 |
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