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pH-sensitivity of YFP provides an intracellular indicator of programmed cell death
BACKGROUND: Programmed cell death (PCD) is an essential process for the life cycle of all multicellular organisms. In higher plants however, relatively little is known about the cascade of genes and signalling molecules responsible for the initiation and execution of PCD. To aid with the discovery a...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009963/ https://www.ncbi.nlm.nih.gov/pubmed/21118545 http://dx.doi.org/10.1186/1746-4811-6-27 |
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author | Young, Bennett Wightman, Raymond Blanvillain, Robert Purcel, Sydney B Gallois, Patrick |
author_facet | Young, Bennett Wightman, Raymond Blanvillain, Robert Purcel, Sydney B Gallois, Patrick |
author_sort | Young, Bennett |
collection | PubMed |
description | BACKGROUND: Programmed cell death (PCD) is an essential process for the life cycle of all multicellular organisms. In higher plants however, relatively little is known about the cascade of genes and signalling molecules responsible for the initiation and execution of PCD. To aid with the discovery and analysis of plant PCD regulators, we have designed a novel cell death assay based on low cytosolic pH as a marker of PCD. RESULTS: The acidification that occurs in the cytosol during plant PCD was monitored by way of the extinction of YFP fluorescence at low pH. This fluorescence was recovered experimentally when bringing the intracellular pH back to 7, demonstrating that there was no protein degradation of YFP. Because it uses YFP, the assay is none-destructive, does not interfere with the PCD process and allows time-lapse studies to be carried out. In addition, changes of sub-cellular localisation can be visualised during PCD using the protein of interest fused to RFP. Coupled to a transient expression system, this pH-based assay can be used to functionally analyse genes involved in PCD, using point mutations or co-expressing PCD regulators. Transfecting mBAX and AtBI-1in onion epidermal cells showed that the pH shift is downstream of PCD suppression by AtBI-1. In addition, this method can be used to score PCD in tissues of stably transformed transgenic lines. As proof of principle, we show the example of YFP extinction during xylogenesis in Arabidopsis. This demonstrates that the assay is applicable to PCD studies in a variety of tissues. CONCLUSIONS: The observation that YFP fluorescence is lost during the plant PCD process provides a new tool to study the genetic regulation and cell biology of the process. In addition, plant cell biologists should make a note of this effect of PCD on YFP fluorescence to avoid misinterpretation of their data and to select a pH insensitive reporter if appropriate. This method represents an efficient and streamlined tool expected to bring insights on the process leading to the pH shift occurring during PCD. |
format | Text |
id | pubmed-3009963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30099632010-12-25 pH-sensitivity of YFP provides an intracellular indicator of programmed cell death Young, Bennett Wightman, Raymond Blanvillain, Robert Purcel, Sydney B Gallois, Patrick Plant Methods Methodology BACKGROUND: Programmed cell death (PCD) is an essential process for the life cycle of all multicellular organisms. In higher plants however, relatively little is known about the cascade of genes and signalling molecules responsible for the initiation and execution of PCD. To aid with the discovery and analysis of plant PCD regulators, we have designed a novel cell death assay based on low cytosolic pH as a marker of PCD. RESULTS: The acidification that occurs in the cytosol during plant PCD was monitored by way of the extinction of YFP fluorescence at low pH. This fluorescence was recovered experimentally when bringing the intracellular pH back to 7, demonstrating that there was no protein degradation of YFP. Because it uses YFP, the assay is none-destructive, does not interfere with the PCD process and allows time-lapse studies to be carried out. In addition, changes of sub-cellular localisation can be visualised during PCD using the protein of interest fused to RFP. Coupled to a transient expression system, this pH-based assay can be used to functionally analyse genes involved in PCD, using point mutations or co-expressing PCD regulators. Transfecting mBAX and AtBI-1in onion epidermal cells showed that the pH shift is downstream of PCD suppression by AtBI-1. In addition, this method can be used to score PCD in tissues of stably transformed transgenic lines. As proof of principle, we show the example of YFP extinction during xylogenesis in Arabidopsis. This demonstrates that the assay is applicable to PCD studies in a variety of tissues. CONCLUSIONS: The observation that YFP fluorescence is lost during the plant PCD process provides a new tool to study the genetic regulation and cell biology of the process. In addition, plant cell biologists should make a note of this effect of PCD on YFP fluorescence to avoid misinterpretation of their data and to select a pH insensitive reporter if appropriate. This method represents an efficient and streamlined tool expected to bring insights on the process leading to the pH shift occurring during PCD. BioMed Central 2010-11-30 /pmc/articles/PMC3009963/ /pubmed/21118545 http://dx.doi.org/10.1186/1746-4811-6-27 Text en Copyright ©2010 Young et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Young, Bennett Wightman, Raymond Blanvillain, Robert Purcel, Sydney B Gallois, Patrick pH-sensitivity of YFP provides an intracellular indicator of programmed cell death |
title | pH-sensitivity of YFP provides an intracellular indicator of programmed cell death |
title_full | pH-sensitivity of YFP provides an intracellular indicator of programmed cell death |
title_fullStr | pH-sensitivity of YFP provides an intracellular indicator of programmed cell death |
title_full_unstemmed | pH-sensitivity of YFP provides an intracellular indicator of programmed cell death |
title_short | pH-sensitivity of YFP provides an intracellular indicator of programmed cell death |
title_sort | ph-sensitivity of yfp provides an intracellular indicator of programmed cell death |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009963/ https://www.ncbi.nlm.nih.gov/pubmed/21118545 http://dx.doi.org/10.1186/1746-4811-6-27 |
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