pGreen: a versatile and flexible binary Ti vector for Agrobacterium-mediated plant transformation
By R. Hellens, E. Edwards, Nicola Leyland, S. Bean, P. Mullineaux. Plant Molecular Biology, 2000
1,668 citations recorded by the source corpus.
Subfields: Biotechnology, Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/14bcdf24b7b4b2c501a0c9ec90bda7cdd1ce32aa
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In Biotechnology
In Molecular Biology
- Kazuko Yamaguchi-Shinozaki
- Kazuo Shinozaki
- K. Nakashima
- Jir□í Friml
- M. Fujita
- Motoaki Seki
- K. Maruyama
- Yusuke Ito
In Plant Science
- Kazuko Yamaguchi-Shinozaki
- Kazuo Shinozaki
- K. Nakashima
- M. Fujita
- Jir□í Friml
- Motoaki Seki
- K. Maruyama
- Lam-Son Phan Tran
Citations in the corpus
- A CRISPR/Cas9 toolkit for multiplex genome editing in plants (2014, methodology): “The pGreen binary vectors were constructed based on a previously reported strategy [41].”
- NAC Transcription Factors, NST1 and NST3, Are Key Regulators of the Formation of Secondary Walls in Woody Tissues of Arabidopsis[W][OA] (2007, background): “These genes and 35S:NST3 were constructed from modified vectors derived from pGreenII0029 (Hellens et al., 2000) and p35SSRDXG (Mitsuda et al., 2006).”
- Rapid, combinatorial analysis of membrane compartments in intact plants with a multicolor marker set. (2009, methodology): “Construction of pNIGEL host vectors pNIGEL vectors are based on the pGREENII vector series (Hellens et al., 2000; http://www.pgreen.ac.uk).”
- Targets of the WRKY53 transcription factor and its role during leaf senescence in Arabidopsis (2004, methodology): “…cDNA fragment that contained the full coding sequence and the 3¢-untranslated region of AtWRKY53 or part of WRKY53 cDNA (position nt 580–880) in sense and antisense orientation separated by an intron into the PRT-W cassette and into pGreen 0229 binary vector, respectively (Hellens et al., 2000).”
- Transient expression vectors for functional genomics, quantification of promoter activity and RNA silencing in plants (2005, methodology): “The PCR products were digested with appropriate restriction enzymes and these two digested PCR products were used in a 3-way ligation to HindIII-BamHI cut pNOS-7 [24] to produce the NOShpLUC cassette.”
- Antagonistic Interaction between Abscisic Acid and Jasmonate-Ethylene Signaling Pathways Modulates Defense Gene Expression and Disease Resistance in Arabidopsis (2004, methodology): “…vector (Hellens et al., 2000) and ligation of the band corresponding to the double 35S promoter/terminator cassette into the pGreenII vector (Hellens et al., 2000) previously linearized by digestion with HindIII, blunt ended using Klenow enzyme, and dephosphorylated using shrimp alkaline…”
- Type 2C protein phosphatases directly regulate abscisic acid-activated protein kinases in Arabidopsis (2009, methodology): “In this study, a series of vector plasmids, such as pGBKT7 and pGADT7 (Clontech), pGEX6P (GE Healthcare), and the pGreen series (30), were converted to Gateway destination vectors.”
- Red colouration in apple fruit is due to the activity of the MYB transcription factor, MdMYB10 (2007, methodology): “…(MP90) transformed with the reporter cassette with 450 ll each of two other Agrobacterium cultures transformed with cassettes containing a MYB TF gene fused to the 35S promoter and a bHLH TF gene in either pART27 (Gleave, 1992) or pGreenII 62- SK binary vectors (Figure S4) (Hellens et al., 2000).”
- The Balance between the MIR164A and CUC2 Genes Controls Leaf Margin Serration in Arabidopsis[W] (2006, methodology): “The various constructs used to complement the mir164a-4 mutant were generated by amplifying several fragments of the MIR164A gene by PCR and reconstructing the gene in the pGreenII0229 binary vector (Hellens et al., 2000).”
- SCARECROW is involved in positioning the stem cell niche in the Arabidopsis root meristem. (2003, neutral): “promoter in the 35S cassette (Hellens et al. 2000).”