T-DNA insertional mutagenesis for functional genomics in rice.

By J. Jeon, Sichul Lee, K. Jung, S. Jun, D. Jeong, Jinwon Lee, Chanhong Kim, S. Jang, Shinyoung Lee, Kiyoung Yang and 11 more. The Plant Journal, 2000

739 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/670350e59c9908fb1524f1a7ef512bc8ab4c761e

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Citations in the corpus

Development of Genetic and Genomic Research Resources for Brachypodium distachyon, a New Model System for Grass Crop Research (2008, neutral): “Agrobacterium-mediated transformation of both rice and Arabidopsis produces an average of approximately 1.5 transgenes per line (Feldmann, 1991; Jeon et al., 2000).”
Physiology and molecular biology of stress tolerance in plants (2006, background): “On the other hand, though a database is available for T-DNA tagging lines of rice, it is not saturated, representing less than 10% the number of lines required (Jeon et al., 2000).”
A genomics approach towards salt stress tolerance (2001, background): “[ 22 , 30]). Functional complementation in model organisms such as Synechocystis, yeast, Aspergillus and Arabidopsis mutants presents a second strategy.”
Advances in Transgenic Rice Biotechnology (2007, background): “Earlier, 22,090 transgenic rice plants with the T-DNA integrated in their genome were generated by Jeon et al . (2000a) with the aim of identifying insertional mutants in various genes and for discovering new genes.”
Functional analysis of a cold-responsive rice WRKY gene, OsWRKY71 (2016, methodology): “…tumefaciens LBA4404 strain harboring this vector was grown on AB media supplemented with 10 mg L -1 streptomycin and 50 mg L -1 hygromycin for 3 days at 28 °C, and transgenic calli were obtained via the Agrobacterium-mediated cocultivation method as described previously (Jeon et al. 2000).”
Cloning Vectors for Rice (2009, background): “In addition to its economic importance, rice is a model for the study of monocot species because it is a diploid, its entire genome has been sequenced [8, 18], and it is easy to transform [11, 15].”
Impact of high-temperature stress on rice plant and its traits related to tolerance (2011, background): “The availability of high-density genetic and physical maps, expressed sequence tags (ESTs), genomic sequences and mutant stocks such as T-DNA insertional mutants (Jeon et al. 2000) have established rice as an excellent model plant for the study of heat tolerance among cereals.”
A CRISPR/Cas9 toolkit for multiplex genome editing in plants (2014, background): “For the majority of researchers, transfer DNA (T-DNA) and transposon insertional mutagenesis remain the main sources of mutants of genes of interest in model plants such as the dicot Arabidopsis thaliana and the monocot rice (Oryza sativa) [1,2].”
The Sequence of 1504 Mutants in the Model Rice Variety Kitaake Facilitates Rapid Functional Genomic Studies (2017, background): “Rice mutants have been generated through TDNA insertion (Jeon et al., 2000; Chen et al., 2003; Sallaud et al., 2003; Wu et al., 2003; Hsing et al., 2007), transposon/retrotransposon insertion (Miyao et al.”
Stress-inducible OsP5CS2 gene is essential for salt and cold tolerance in rice (2004, methodology): “[29].”
Rice phenolics efflux transporter 2 (PEZ2) plays an important role in solubilizing apoplasmic iron (2011, positive): “We obtained 50 independent T-DNA mutants from the rice T-DNA insertion sequence database (http:// www.postech.ac.kr/life/pfg/risd/index.html) potentially related to Cd transport on the basis of changes in expression in response to Cd (Ogawa et al. 2009; Jeon et al. 2000; Jeong et al. 2006).”
Agrobacterium-mediated transformation and inbred line development in the model grass Brachypodium distachyon (2006, background): “This data is consistent with that found in other systems where Agrobacterium-mediated transformation results in transgene integration at an average of 1.5 loci per line for Arabidopsis and 1.4 loci for rice (Feldmann 1991; Jeon et al., 2000).”