Literature DB >> 8528289

Green-fluorescent protein as a new vital marker in plant cells.

J Sheen1, S Hwang, Y Niwa, H Kobayashi, D W Galbraith.   

Abstract

The green-fluorescent protein (GFP) from jellyfish Aequorea victoria has been used as a convenient new vital marker in various heterologous systems. However, it has been problematic to express GFP in higher eukaryotes, especially in higher plants. This paper reports that either a strong constitutive or a heat-shock promoter can direct the expression of GFP which is easily detectable in maize mesophyll protoplasts. In this single-cell system, bright green fluorescence emitted from GFP is visible when excited with UV or blue light even in the presence of blue fluorescence from the vacuole or the red chlorophyll autofluorescence from chloroplasts using a fluorescence microscope. No exogenous substrate, co-factor, or other gene product is required. GFP is very stable in plant cells and shows little photobleaching. Viable cells can be obtained after fluorescence-activated cell sorting based on GFP. The paper further reports that GFP can be detected in intact tissues after delivering the constructs into Arabidopsis leaf and root by microprojectile bombardment. The successful detection of GFP in plant cells relies on the use of a universal transcription enhancer from maize or the translation enhancer from tobacco mosaic virus (TMV) to boost the expression. This new reporter could be used to monitor gene expression, signal transduction, co-transfection, transformation, protein trafficking and localization, protein-protein interaction, cell separation and purification, and cell lineage in higher plants.

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Year:  1995        PMID: 8528289     DOI: 10.1046/j.1365-313x.1995.08050777.x

Source DB:  PubMed          Journal:  Plant J        ISSN: 0960-7412            Impact factor:   6.417


  85 in total

Review 1.  Plant transformation technology. Developments and applications.

Authors:  C A Newell
Journal:  Mol Biotechnol       Date:  2000-09       Impact factor: 2.695

2.  Use of green fluorescent protein-conjugated beta-actin as a novel molecular marker for in vitro tumor cell chemotaxis assay.

Authors:  L Hodgson; W Qiu; C Dong; A J Henderson
Journal:  Biotechnol Prog       Date:  2000 Nov-Dec

Review 3.  Green fluorescent protein is lighting up fungal biology.

Authors:  J M Lorang; R P Tuori; J P Martinez; T L Sawyer; R S Redman; J A Rollins; T J Wolpert; K B Johnson; R J Rodriguez; M B Dickman; L M Ciuffetti
Journal:  Appl Environ Microbiol       Date:  2001-05       Impact factor: 4.792

4.  Functional analysis of two maize cDNAs encoding T7-like RNA polymerases.

Authors:  C C Chang; J Sheen; M Bligny; Y Niwa; S Lerbs-Mache; D B Stern
Journal:  Plant Cell       Date:  1999-05       Impact factor: 11.277

5.  Cotransformation of Trichoderma harzianum with beta-glucuronidase and green fluorescent protein genes provides a useful tool for monitoring fungal growth and activity in natural soils.

Authors:  Y S Bae; G R Knudsen
Journal:  Appl Environ Microbiol       Date:  2000-02       Impact factor: 4.792

6.  High molecular weight RNAs and small interfering RNAs induce systemic posttranscriptional gene silencing in plants.

Authors:  Ulrich Klahre; Patrice Crété; Sabrina A Leuenberger; Victor A Iglesias; Frederick Meins
Journal:  Proc Natl Acad Sci U S A       Date:  2002-08-14       Impact factor: 11.205

7.  Jellyfish green fluorescent protein as a useful reporter for transient expression and stable transformation in Medicago sativa L.

Authors:  M Bellucci; F De Marchis; R Mannucci; S Arcioni
Journal:  Plant Cell Rep       Date:  2003-08-22       Impact factor: 4.570

8.  Autophosphorylation and subcellular localization dynamics of a salt- and water deficit-induced calcium-dependent protein kinase from ice plant.

Authors:  E Wassim Chehab; O Rahul Patharkar; Adrian D Hegeman; Tahar Taybi; John C Cushman
Journal:  Plant Physiol       Date:  2004-07-09       Impact factor: 8.340

9.  Generation of T-DNA tagging lines with a bidirectional gene trap vector and the establishment of an insertion-site database.

Authors:  Choong-Hwan Ryu; Jung-Hwa You; Hong-Gyu Kang; Junghe Hur; Young-Hea Kim; Min-Jung Han; Kyungsook An; Byoung-Chull Chung; Choon-Hwan Lee; Gynheung An
Journal:  Plant Mol Biol       Date:  2004-03       Impact factor: 4.076

10.  An improved protocol for Agrobacterium-mediated transformation of Antirrhinum majus L.

Authors:  M-L Cui; T Handa; H Ezura
Journal:  Mol Genet Genomics       Date:  2003-09-26       Impact factor: 3.291

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