A high-throughput method for detection of DNA in chloroplasts using flow cytometry

<p>Abstract</p> <p>Background</p> <p>The amount of DNA in the chloroplasts of some plant species has been shown recently to decline dramatically during leaf development. A high-throughput method of DNA detection in chloroplasts is now needed in order to facilitate the f...

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Main Authors: Oldenburg Delene J, Rowan Beth A, Bendich Arnold J
Format: Article
Language:English
Published: BMC 2007-03-01
Series:Plant Methods
Online Access:http://www.plantmethods.com/content/3/1/5
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spelling doaj-0f7eeaeca4d940c3bbb0c2ce2a530e572020-11-25T00:33:43ZengBMCPlant Methods1746-48112007-03-0131510.1186/1746-4811-3-5A high-throughput method for detection of DNA in chloroplasts using flow cytometryOldenburg Delene JRowan Beth ABendich Arnold J<p>Abstract</p> <p>Background</p> <p>The amount of DNA in the chloroplasts of some plant species has been shown recently to decline dramatically during leaf development. A high-throughput method of DNA detection in chloroplasts is now needed in order to facilitate the further investigation of this process using large numbers of tissue samples.</p> <p>Results</p> <p>The DNA-binding fluorophores 4',6-diamidino-2-phenylindole (DAPI), SYBR Green I (SG), SYTO 42, and SYTO 45 were assessed for their utility in flow cytometric analysis of DNA in Arabidopsis chloroplasts. Fluorescence microscopy and real-time quantitative PCR (qPCR) were used to validate flow cytometry data. We found neither DAPI nor SYTO 45 suitable for flow cytometric analysis of chloroplast DNA (cpDNA) content, but did find changes in cpDNA content during development by flow cytometry using SG and SYTO 42. The latter dye provided more sensitive detection, and the results were similar to those from the fluorescence microscopic analysis. Differences in SYTO 42 fluorescence were found to correlate with differences in cpDNA content as determined by qPCR using three primer sets widely spaced across the chloroplast genome, suggesting that the whole genome undergoes copy number reduction during development, rather than selective reduction/degradation of subgenomic regions.</p> <p>Conclusion</p> <p>Flow cytometric analysis of chloroplasts stained with SYTO 42 is a high-throughput method suitable for determining changes in cpDNA content during development and for sorting chloroplasts on the basis of DNA content.</p> http://www.plantmethods.com/content/3/1/5
collection DOAJ
language English
format Article
sources DOAJ
author Oldenburg Delene J
Rowan Beth A
Bendich Arnold J
spellingShingle Oldenburg Delene J
Rowan Beth A
Bendich Arnold J
A high-throughput method for detection of DNA in chloroplasts using flow cytometry
Plant Methods
author_facet Oldenburg Delene J
Rowan Beth A
Bendich Arnold J
author_sort Oldenburg Delene J
title A high-throughput method for detection of DNA in chloroplasts using flow cytometry
title_short A high-throughput method for detection of DNA in chloroplasts using flow cytometry
title_full A high-throughput method for detection of DNA in chloroplasts using flow cytometry
title_fullStr A high-throughput method for detection of DNA in chloroplasts using flow cytometry
title_full_unstemmed A high-throughput method for detection of DNA in chloroplasts using flow cytometry
title_sort high-throughput method for detection of dna in chloroplasts using flow cytometry
publisher BMC
series Plant Methods
issn 1746-4811
publishDate 2007-03-01
description <p>Abstract</p> <p>Background</p> <p>The amount of DNA in the chloroplasts of some plant species has been shown recently to decline dramatically during leaf development. A high-throughput method of DNA detection in chloroplasts is now needed in order to facilitate the further investigation of this process using large numbers of tissue samples.</p> <p>Results</p> <p>The DNA-binding fluorophores 4',6-diamidino-2-phenylindole (DAPI), SYBR Green I (SG), SYTO 42, and SYTO 45 were assessed for their utility in flow cytometric analysis of DNA in Arabidopsis chloroplasts. Fluorescence microscopy and real-time quantitative PCR (qPCR) were used to validate flow cytometry data. We found neither DAPI nor SYTO 45 suitable for flow cytometric analysis of chloroplast DNA (cpDNA) content, but did find changes in cpDNA content during development by flow cytometry using SG and SYTO 42. The latter dye provided more sensitive detection, and the results were similar to those from the fluorescence microscopic analysis. Differences in SYTO 42 fluorescence were found to correlate with differences in cpDNA content as determined by qPCR using three primer sets widely spaced across the chloroplast genome, suggesting that the whole genome undergoes copy number reduction during development, rather than selective reduction/degradation of subgenomic regions.</p> <p>Conclusion</p> <p>Flow cytometric analysis of chloroplasts stained with SYTO 42 is a high-throughput method suitable for determining changes in cpDNA content during development and for sorting chloroplasts on the basis of DNA content.</p>
url http://www.plantmethods.com/content/3/1/5
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