Expression and molecular analysis of DsRed and gfp fluorescent genes in tobacco (Nicotiana tabacum L.)

Agrobacterium-mediated transformation of tobacco leaf disks with Agrobacterium tumefaciens (A. t.) strain LBA4404 and two plasmids (pCAMBIA1390-DsRed and pART27 2mgfp5-ER) was used for introducing red fluorescent gene (DsRed), green fluorescent gene (gfp) and corresponding selection genes (hptII for...

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Main Authors: Kati OVEN, Zlata LUTHAR
Format: Article
Language:English
Published: University of Ljubljana Press (Založba Univerze v Ljubljani) 2013-04-01
Series:Acta Agriculturae Slovenica
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Online Access:https://journals.uni-lj.si/aas/article/view/14938
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author Kati OVEN
Zlata LUTHAR
author_facet Kati OVEN
Zlata LUTHAR
author_sort Kati OVEN
collection DOAJ
description Agrobacterium-mediated transformation of tobacco leaf disks with Agrobacterium tumefaciens (A. t.) strain LBA4404 and two plasmids (pCAMBIA1390-DsRed and pART27 2mgfp5-ER) was used for introducing red fluorescent gene (DsRed), green fluorescent gene (gfp) and corresponding selection genes (hptII for resistance to antibiotic hygromycin and nptII for resistance to kanamycin) into leaf discs of tobacco (Nicotiana tabacum L.). Epifluorescent microscopy with the appropriate set of filters did not reveal phenotypic expression of the DsRed gene in 6.9 % of regenerants and the gfp gene in 1.3 % of regenerants that were successfully grown on selective medium. The duplex PCR method also did not confirm the presence of fragments specific to DsRed or gfp genes in these regenerants, while the presence of fragments characteristic of selection genes hptII and nptII was confirmed. A built-in nptII gene mutation, a deletion, was detected in one regenerant. Out of the 139 regenerants generated after the transformation of A. t.-pCAMBIA1390-DsRed, 38 or 25.5 % successfully grew only on non-selective medium; after transformation with A. t.-pART27 2mgfp5-ER 9 or 5.4 % of the 161 generants grew successfully. PCR analysis confirmed in all regenerants the presence of fragments characteristic of both transgenes, which were not expressed or were silenced. The effectiveness of transformation after infection with A. t.-pCAMBIA1390-DsRed was 93.1 %, and 98.7 % after infection with A. t.-pART27 2mgfp5-ER. We established that both fluorescent genes are suitable for setting up a transformation system. The antibiotics hygromycin and kanamycin successfully prevented the growth of untransformed tissues, but the antibiotic timentin successfully prevented the growth of bacteria A. t. after the transformation.
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spelling doaj-art-653fb35ef0134201a9dde42de59cd0a52025-08-20T02:52:55ZengUniversity of Ljubljana Press (Založba Univerze v Ljubljani)Acta Agriculturae Slovenica1854-19412013-04-01101151410.14720/aas.2013.101.1.1493821330Expression and molecular analysis of DsRed and gfp fluorescent genes in tobacco (Nicotiana tabacum L.)Kati OVEN0Zlata LUTHAR1Ljubljanska cesta 8, 1293 Šmarje - Sap, SloveniaDepartment of Agronomy, Biotechnical Faculty, University of Ljubljana, Jamnikarjeva 101, SI-1000 Ljubljana, SloveniaAgrobacterium-mediated transformation of tobacco leaf disks with Agrobacterium tumefaciens (A. t.) strain LBA4404 and two plasmids (pCAMBIA1390-DsRed and pART27 2mgfp5-ER) was used for introducing red fluorescent gene (DsRed), green fluorescent gene (gfp) and corresponding selection genes (hptII for resistance to antibiotic hygromycin and nptII for resistance to kanamycin) into leaf discs of tobacco (Nicotiana tabacum L.). Epifluorescent microscopy with the appropriate set of filters did not reveal phenotypic expression of the DsRed gene in 6.9 % of regenerants and the gfp gene in 1.3 % of regenerants that were successfully grown on selective medium. The duplex PCR method also did not confirm the presence of fragments specific to DsRed or gfp genes in these regenerants, while the presence of fragments characteristic of selection genes hptII and nptII was confirmed. A built-in nptII gene mutation, a deletion, was detected in one regenerant. Out of the 139 regenerants generated after the transformation of A. t.-pCAMBIA1390-DsRed, 38 or 25.5 % successfully grew only on non-selective medium; after transformation with A. t.-pART27 2mgfp5-ER 9 or 5.4 % of the 161 generants grew successfully. PCR analysis confirmed in all regenerants the presence of fragments characteristic of both transgenes, which were not expressed or were silenced. The effectiveness of transformation after infection with A. t.-pCAMBIA1390-DsRed was 93.1 %, and 98.7 % after infection with A. t.-pART27 2mgfp5-ER. We established that both fluorescent genes are suitable for setting up a transformation system. The antibiotics hygromycin and kanamycin successfully prevented the growth of untransformed tissues, but the antibiotic timentin successfully prevented the growth of bacteria A. t. after the transformation.https://journals.uni-lj.si/aas/article/view/14938nicotiana tabacumfluorescent genesselection genestransformationexspression of transgenesdna analysis
spellingShingle Kati OVEN
Zlata LUTHAR
Expression and molecular analysis of DsRed and gfp fluorescent genes in tobacco (Nicotiana tabacum L.)
Acta Agriculturae Slovenica
nicotiana tabacum
fluorescent genes
selection genes
transformation
exspression of transgenes
dna analysis
title Expression and molecular analysis of DsRed and gfp fluorescent genes in tobacco (Nicotiana tabacum L.)
title_full Expression and molecular analysis of DsRed and gfp fluorescent genes in tobacco (Nicotiana tabacum L.)
title_fullStr Expression and molecular analysis of DsRed and gfp fluorescent genes in tobacco (Nicotiana tabacum L.)
title_full_unstemmed Expression and molecular analysis of DsRed and gfp fluorescent genes in tobacco (Nicotiana tabacum L.)
title_short Expression and molecular analysis of DsRed and gfp fluorescent genes in tobacco (Nicotiana tabacum L.)
title_sort expression and molecular analysis of dsred and gfp fluorescent genes in tobacco nicotiana tabacum l
topic nicotiana tabacum
fluorescent genes
selection genes
transformation
exspression of transgenes
dna analysis
url https://journals.uni-lj.si/aas/article/view/14938
work_keys_str_mv AT katioven expressionandmolecularanalysisofdsredandgfpfluorescentgenesintobacconicotianatabacuml
AT zlataluthar expressionandmolecularanalysisofdsredandgfpfluorescentgenesintobacconicotianatabacuml