Literature DB >> 17768628

Sample topography and position within plant body influence the detection of the intensity of green fluorescent protein fluorescence in the leaves of transgenic tobacco plants.

Marek Hraska1, Veronika Hermanová, Slavomír Rakouský, Vladislav Curn.   

Abstract

The effect of the type of leaf tissue selected for the study of green fluorescent protein (GFP) fluorescence intensity was investigated here using the T(1) generation of transgenic tobacco expressing the m-gfp5-ER gene. The fluorescence of GFP was detected by fluorescence binocular microscope coupled with the CCD camera and quantified by means of image analyses using the Lucia((R)) software. Mean brightness values from various leaf tissues were compared. First, an original data revealing the significant differences in the fluorescence intensity between the abaxial and adaxial surfaces are given. Stronger signal was detected on the abaxial side. Subsequently, the effect of the tissue location within the leaf surface was investigated and higher fluorescence was detected on the samples detached from leaf tips. Finally, the effect of the physiological age of leaves was studied using the in vitro clonally propagated plants. Leaves from the analogous positions within the plant body of three clones were investigated. The decrease in the fluorescence towards the plant top (youngest leaves) was observed in all studied plants. Surprisingly, the variability of the fluorescence within the clones of studied genotype was high enough to conclude, that the fluorescence of each individual is unique and affected by particular genotype and environment. Our study showed that the origin of leaf tissue selected for the GFP quantification is crucial and that the fluctuations in the fluorescence intensity should be taken into account when comparing the GFP fluorescence patterns of different plants. Moreover, the degree of fluorescence variability seems to be individually affected.

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Year:  2007        PMID: 17768628     DOI: 10.1007/s00299-007-0431-7

Source DB:  PubMed          Journal:  Plant Cell Rep        ISSN: 0721-7714            Impact factor:   4.570


  7 in total

1.  Developmental and tissue-specific expression of CaMV 35S promoter in cotton as revealed by GFP.

Authors:  Ganesan Sunilkumar; LeAnne Mohr; Emily Lopata-Finch; Chandrakanth Emani; Keerti S Rathore
Journal:  Plant Mol Biol       Date:  2002-10       Impact factor: 4.076

2.  Regulated genes in transgenic plants.

Authors:  P N Benfey; N H Chua
Journal:  Science       Date:  1989-04-14       Impact factor: 47.728

3.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

4.  The dark side of green fluorescent protein.

Authors:  Xin Zhou; Raul Carranco; Stanislav Vitha; Timothy C Hall
Journal:  New Phytol       Date:  2005-11       Impact factor: 10.151

5.  Endosperm-specific expression of green fluorescent protein driven by the hordein promoter is stably inherited in transgenic barley (Hordeum vulgare) plants.

Authors:  Myeong-Je Cho; Hae-Woon Choi; Wen Jiang; Chi D Ha; Peggy G Lemaux
Journal:  Physiol Plant       Date:  2002-05       Impact factor: 4.500

6.  A simple and general method for transferring genes into plants.

Authors: 
Journal:  Science       Date:  1985-03-08       Impact factor: 47.728

7.  Spatial and temporal patterns of green fluorescent protein (GFP) fluorescence during leaf canopy development in transgenic oilseed rape, Brassica napus L.

Authors:  M D Halfhill; R J Millwood; T W Rufty; A K Weissinger; C N Stewart
Journal:  Plant Cell Rep       Date:  2003-09-04       Impact factor: 4.570

  7 in total
  3 in total

1.  Effect of ploidy increase on transgene expression: example from Citrus diploid cybrid and allotetraploid somatic hybrid expressing the EGFP gene.

Authors:  Shi-Xiao Xu; Xiao-Dong Cai; Bin Tan; Ding-Li Li; Wen-Wu Guo
Journal:  Protoplasma       Date:  2010-08-24       Impact factor: 3.356

2.  ER disruption and GFP degradation during non-regenerable transformation of flax with Agrobacterium tumefaciens.

Authors:  Juraj Bleho; Bohuš Obert; Tomáš Takáč; Beáta Petrovská; Claudia Heym; Diedrik Menzel; Jozef Samaj
Journal:  Protoplasma       Date:  2011-01-26       Impact factor: 3.356

3.  An epifluorescent attachment improves whole-plant digital photography of Arabidopsis thaliana expressing red-shifted green fluorescent protein.

Authors:  Stokes S Baker; Cleo B Vidican; David S Cameron; Haittam G Greib; Christine C Jarocki; Andres W Setaputri; Christopher H Spicuzza; Aaron A Burr; Meriam A Waqas; Danzell A Tolbert
Journal:  AoB Plants       Date:  2012-03-06       Impact factor: 3.276

  3 in total

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