Literature DB >> 19093120

A simple and sensitive high-throughput GFP screening in woody and herbaceous plants.

Jean-Michel Hily1, Zongrang Liu.   

Abstract

Green fluorescent protein (GFP) has been used widely as a powerful bioluminescent reporter, but its visualization by existing methods in tissues or whole plants and its utilization for high-throughput screening remains challenging in many species. Here, we report a fluorescence image analyzer-based method for GFP detection and its utility for high-throughput screening of transformed plants. Of three detection methods tested, the Typhoon fluorescence scanner was able to detect GFP fluorescence in all Arabidopsis thaliana tissues and apple leaves, while regular fluorescence microscopy detected it only in Arabidopsis flowers and siliques but barely in the leaves of either Arabidopsis or apple. The hand-held UV illumination method failed in all tissues of both species. Additionally, the Typhoon imager was able to detect GFP fluorescence in both green and non-green tissues of Arabidopsis seedlings as well as in imbibed seeds, qualifying it as a high-throughput screening tool, which was further demonstrated by screening the seedlings of primary transformed T(0) seeds. Of the 30,000 germinating Arabidopsis seedlings screened, at least 69 GFP-positive lines were identified, accounting for an approximately 0.23% transformation efficiency. About 14,000 seedlings grown in 16 Petri plates could be screened within an hour, making the screening process significantly more efficient and robust than any other existing high-throughput screening method for transgenic plants.

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Year:  2008        PMID: 19093120     DOI: 10.1007/s00299-008-0657-z

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


  50 in total

1.  High-throughput screening for isolation of enhanced green fluorescent protein expressing transformants of filamentous fungus using an image analyzer.

Authors:  Satoshi Suzuki; Hiroko Taketani; Ken-Ichi Kusumoto; Yutaka Kashiwagi
Journal:  J Biosci Bioeng       Date:  2003       Impact factor: 2.894

2.  Green fluorescent protein as a marker to investigate targeting of organellar RNA polymerases of higher plants in vivo.

Authors:  B Hedtke; M Meixner; S Gillandt; E Richter; T Börner; A Weihe
Journal:  Plant J       Date:  1999-03       Impact factor: 6.417

3.  Green fluorescent protein as a marker for gene expression.

Authors:  M Chalfie; Y Tu; G Euskirchen; W W Ward; D C Prasher
Journal:  Science       Date:  1994-02-11       Impact factor: 47.728

4.  Potato virus X amplicons in arabidopsis mediate genetic and epigenetic gene silencing.

Authors:  T Dalmay; A Hamilton; E Mueller; D C Baulcombe
Journal:  Plant Cell       Date:  2000-03       Impact factor: 11.277

5.  Genetic analysis of osmotic and cold stress signal transduction in Arabidopsis: interactions and convergence of abscisic acid-dependent and abscisic acid-independent pathways.

Authors:  M Ishitani; L Xiong; B Stevenson; J K Zhu
Journal:  Plant Cell       Date:  1997-11       Impact factor: 11.277

6.  Removal of a cryptic intron and subcellular localization of green fluorescent protein are required to mark transgenic Arabidopsis plants brightly.

Authors:  J Haseloff; K R Siemering; D C Prasher; S Hodge
Journal:  Proc Natl Acad Sci U S A       Date:  1997-03-18       Impact factor: 11.205

7.  Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana.

Authors:  S J Clough; A F Bent
Journal:  Plant J       Date:  1998-12       Impact factor: 6.417

8.  Use of green fluorescent protein to visualize the early events of symbiosis between Rhizobium meliloti and alfalfa (Medicago sativa).

Authors:  D J Gage; T Bobo; S R Long
Journal:  J Bacteriol       Date:  1996-12       Impact factor: 3.490

9.  An optimal pooling strategy applied to high-throughput screening for rare marker-free transformants.

Authors:  Jinrui Zhang; Qin Xiao; Kexiu Li; Mingjie Chen; Junli Chang; Liting Luo; Yang Li; Yong Liu; Peter R Shewry; Guangyuan He
Journal:  Biotechnol Lett       Date:  2006-08-11       Impact factor: 2.461

10.  Live cell imaging of repetitive DNA sequences via GFP-tagged polydactyl zinc finger proteins.

Authors:  Beatrice I Lindhout; Paul Fransz; Federico Tessadori; Tobias Meckel; Paul J J Hooykaas; Bert J van der Zaal
Journal:  Nucleic Acids Res       Date:  2007-08-17       Impact factor: 16.971

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  5 in total

1.  Analysis of the enhancer-blocking function of the TBS element from Petunia hybrida in transgenic Arabidopsis thaliana and Nicotiana tabacum.

Authors:  Stacy D Singer; Jean-Michel Hily; Kerik D Cox
Journal:  Plant Cell Rep       Date:  2011-06-26       Impact factor: 4.570

2.  Fluorescence-based methods for measuring target interference by CRISPR-Cas systems.

Authors:  Phong T Phan; Michael Schelling; Chaoyou Xue; Dipali G Sashital
Journal:  Methods Enzymol       Date:  2018-12-21       Impact factor: 1.600

3.  Both the constitutive cauliflower mosaic virus 35S and tissue-specific AGAMOUS enhancers activate transcription autonomously in Arabidopsis thaliana.

Authors:  Stacy D Singer; Kerik D Cox; Zongrang Liu
Journal:  Plant Mol Biol       Date:  2010-08-12       Impact factor: 4.076

4.  The sucrose synthase-1 promoter from Citrus sinensis directs expression of the β-glucuronidase reporter gene in phloem tissue and in response to wounding in transgenic plants.

Authors:  Stacy D Singer; Jean-Michel Hily; Kerik D Cox
Journal:  Planta       Date:  2011-05-19       Impact factor: 4.116

5.  A transformation booster sequence (TBS) from Petunia hybrida functions as an enhancer-blocking insulator in Arabidopsis thaliana.

Authors:  Jean-Michel Hily; Stacy D Singer; Yazhou Yang; Zongrang Liu
Journal:  Plant Cell Rep       Date:  2009-04-17       Impact factor: 4.570

  5 in total

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