In vivo labelling of Anagallis arvensis L. cells with green fluorescent protein

A few methods only enable to follow the fate of plant cells in vivo. One of the most promising is using the Green Fluorescent Protein (GFP). In our preliminary study we set up the experimental system enabling labelling of Anagallis arvensis cells with this marker. We prepared an expression plasmid c...

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Main Authors: Marcin Łukaszewicz, Dorota Kwiatkowska
Format: Article
Language:English
Published: Polish Botanical Society 2014-01-01
Series:Acta Societatis Botanicorum Poloniae
Subjects:
Online Access:https://pbsociety.org.pl/journals/index.php/asbp/article/view/710
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spelling doaj-abe9a998de304841991edf12b69236972020-11-25T03:44:11ZengPolish Botanical SocietyActa Societatis Botanicorum Poloniae2083-94802014-01-01692859110.5586/asbp.2000.010497In vivo labelling of Anagallis arvensis L. cells with green fluorescent proteinMarcin Łukaszewicz0Dorota Kwiatkowska1Wrocław UniversityWrocław UniversityA few methods only enable to follow the fate of plant cells in vivo. One of the most promising is using the Green Fluorescent Protein (GFP). In our preliminary study we set up the experimental system enabling labelling of Anagallis arvensis cells with this marker. We prepared an expression plasmid containing red-shifted gfp with optimised translation start site context, under the control of CaMV 35S transcription promoter. The construct was introduced into A. arvensis cells by particle bombardment. We developed two methods of material preparation for this transformation: in vitro cultured stem internodes with regenerating adventitious shoots (the earliest stages of regeneration); and shoot tips with temporarily exposed apices. The reflected light fluorescence microscope Olympus with the set of filters U-MNB designed for fluorescein detection enables the observation of GFP fluorescence. Both ordinary epidermal cells and stomata guard cells were transformed. Their fluorescence was observed for up to 14 days. Artefacts (autofluorescence of glandular trichomes and faint green glowing of meristematic tissue) could be overcome by the optimisation of the filter set.https://pbsociety.org.pl/journals/index.php/asbp/article/view/710gfp gene markerbiolistic transformationcell labellingAnagallis arvensis
collection DOAJ
language English
format Article
sources DOAJ
author Marcin Łukaszewicz
Dorota Kwiatkowska
spellingShingle Marcin Łukaszewicz
Dorota Kwiatkowska
In vivo labelling of Anagallis arvensis L. cells with green fluorescent protein
Acta Societatis Botanicorum Poloniae
gfp gene marker
biolistic transformation
cell labelling
Anagallis arvensis
author_facet Marcin Łukaszewicz
Dorota Kwiatkowska
author_sort Marcin Łukaszewicz
title In vivo labelling of Anagallis arvensis L. cells with green fluorescent protein
title_short In vivo labelling of Anagallis arvensis L. cells with green fluorescent protein
title_full In vivo labelling of Anagallis arvensis L. cells with green fluorescent protein
title_fullStr In vivo labelling of Anagallis arvensis L. cells with green fluorescent protein
title_full_unstemmed In vivo labelling of Anagallis arvensis L. cells with green fluorescent protein
title_sort in vivo labelling of anagallis arvensis l. cells with green fluorescent protein
publisher Polish Botanical Society
series Acta Societatis Botanicorum Poloniae
issn 2083-9480
publishDate 2014-01-01
description A few methods only enable to follow the fate of plant cells in vivo. One of the most promising is using the Green Fluorescent Protein (GFP). In our preliminary study we set up the experimental system enabling labelling of Anagallis arvensis cells with this marker. We prepared an expression plasmid containing red-shifted gfp with optimised translation start site context, under the control of CaMV 35S transcription promoter. The construct was introduced into A. arvensis cells by particle bombardment. We developed two methods of material preparation for this transformation: in vitro cultured stem internodes with regenerating adventitious shoots (the earliest stages of regeneration); and shoot tips with temporarily exposed apices. The reflected light fluorescence microscope Olympus with the set of filters U-MNB designed for fluorescein detection enables the observation of GFP fluorescence. Both ordinary epidermal cells and stomata guard cells were transformed. Their fluorescence was observed for up to 14 days. Artefacts (autofluorescence of glandular trichomes and faint green glowing of meristematic tissue) could be overcome by the optimisation of the filter set.
topic gfp gene marker
biolistic transformation
cell labelling
Anagallis arvensis
url https://pbsociety.org.pl/journals/index.php/asbp/article/view/710
work_keys_str_mv AT marcinłukaszewicz invivolabellingofanagallisarvensislcellswithgreenfluorescentprotein
AT dorotakwiatkowska invivolabellingofanagallisarvensislcellswithgreenfluorescentprotein
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