Signal transduction in maize and Arabidopsis mesophyll protoplasts.
By Jen Sheen. Plant Physiology, 2001
697 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/eaa429fdf965839f969850913783149c3322e75c
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Citations in the corpus
- Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis (2007, background): “More general information about plant protoplasts can be found in a revie”
- The MYB46 Transcription Factor Is a Direct Target of SND1 and Regulates Secondary Wall Biosynthesis in Arabidopsis (2007, methodology): “duced into Arabidopsis leaf protoplasts by polyethylene glycol‐mediated transfection according to Sheen (2001) .”
- Sugar Sensing and Signaling in Plants Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.010455. (2002, background): “Further characterization of the auxin and cytokinin signaling components (Guilfoyle et al., 1998; Gray and Estelle, 2000; Hwang and Sheen, 2001; Mok and Mok, 2001) should reveal the molecular mechanisms that underlie their interactions with the sugar signal transduction pathway.”
- Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, positive): “Protein localization AtZIP1 and AtZIP2 were cloned into the pSAT1 enhanced green fluorescent protein (eGFP) expression vector in-frame with the C-terminus of eGFP using the KpnI site, and transiently expressed in freshly isolated protoplasts from 3- to 4-week-old Arabidopsis seedlings according to S”
- A simple and effective method for protein subcellular localization using Agrobacterium-mediated transformation of onion epidermal cells (2007, background): “How- ever, the suspension-cultured cells and protoplasts as well as the stable transformation are time-consuming, expensive and need high proficiency of special techniques and great patience (Scott et al. 1999; Sheen 2001).”
- MYB58 and MYB63 Are Transcriptional Activators of the Lignin Biosynthetic Pathway during Secondary Cell Wall Formation in Arabidopsis[C][W] (2009, methodology): “The reporter and effector constructs were cotransfected into Arabidopsis leaf protoplasts (Sheen, 2001).”
- A Battery of Transcription Factors Involved in the Regulation of Secondary Cell Wall Biosynthesis in Arabidopsis (2008, methodology): “The SND1-HER expression construct was introduced into Arabidopsis leaf protoplasts alone or together with the MYB46P:GUS construct (Sheen, 2001).”
- The FAST technique: a simplified Agrobacterium-based transformation method for transient gene expression analysis in seedlings of Arabidopsis and other plant species (2009, background): “Routine transient assays include biolistic bombardment [4], protoplast transfection [5], and Agrobacterium-mediated transient assays [6], each with advantages and disadvantages depending on the research goals.”
- MAP kinase signalling cascade in Arabidopsis innate immunity (2002, methodology): “Early defence gene transcription To dissect the early signal transduction pathways in plant innate immune responses, we first established a leaf cell assay based on flg22 inducible transcription of early response genes in Arabidopsis mesophyll protoplast”
- Mesoporous silica nanoparticles deliver DNA and chemicals into plants. (2007, methodology): “We first investigated the use of MSN on protoplasts (plant cells with the cell wall removed), which are often used as model systems in physiological and cellular process studie”
- An efficient cucumber (Cucumis sativus L.) protoplast isolation and transient expression system (2013, background): “Therein, PEG-mediated protoplast transient expression has high transformation efficiency, so it is widely applied in plant molecular biology studies (Sheen, 2001; Walter et al., 2004).”
- A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes (2011, background): “Arabidopsis, maize [3] and tobacco protoplasts [4], tobacco leaf epidermal cells [5], tobacco BY-2 cells [6] and onion epidermal cells [7] are commonly used for transient assays in gene expression, protein subcellular localization, protein-protein interaction and protein activity studies.”
- Targets of the WRKY53 transcription factor and its role during leaf senescence in Arabidopsis (2004, methodology): “Transient expression analyses were performed with Arabidopsis mesophyll protoplast as described by Sheen (2001).”