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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Polish Botanical Society
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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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