Arabidopsis CBF3/DREB1A and ABF3 in Transgenic Rice Increased Tolerance to Abiotic Stress without Stunting Growth1[w]

By Se-Jun Oh, S. Song, Youn Shic Kim, Hyun-Jun Jang, S. Kim, Minjeong Kim, Yeon-Ki Kim, B. Nahm, Jukon Kim. Plant Physiology, 2005

671 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/50c4a2125d72d23695f516ed7501f2b3c7efb79f

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Citations in the corpus

Understanding Abiotic Stress Tolerance Mechanisms: Recent Studies on Stress Response in Rice (2007, background): “Nakdong enhanced tolerance to abiotic stress without inhibiting growth or causing phenotypic alterations (Oh et al. 2005).”
Stress-inducible expression of GmDREB1 conferred salt tolerance in transgenic alfalfa (2010, background): “2007), AtDREB1A in rice (Oh et al. 2005) and AhDREB1 in tobacco (Shen et al.”
Genetic engineering and breeding of drought-resistant crops. (2014, background): “Arabidopsis DREB1A, -1B, and -1C and rice OsDREB1A, -1B, -1E, -1F, and -1G driven either by the CaMV35S, ZmUbi, or OsActin1p promoters or by the drought-inducible HVA22P promoter have been transformed in rice or other crops, and the transgenic plants showed increased DT in greenhouse and field trial”
Plant Responses to Simultaneous Biotic and Abiotic Stress: Molecular Mechanisms (2014, background): “Transgenic Arabidopsis overproducing the NAC transcription factor NTL6, which is induced by cold stress, enhance their defense response against pathogen attack by promoting an up-regulation of the PR1 gene [118–124].”
Transcriptional regulatory networks in cellular responses and tolerance to dehydration and cold stresses. (2006, background): “(82) reported that constitutive overexpression of DREB1A using the 35S promoter in transgenic rice resulted in increased stress tolerance to drought and high salinity.”
Drought tolerance improvement in crop plants: An integrated view from breeding to genomics (2008, background): “On the contrary, CBF3/DREB1A in transgenic rice increased drought and salinity tolerance without affecting growth undesirably (Oh et al., 2005).”
Abiotic Stress Responses in Plants: Unraveling the Complexity of Genes and Networks to Survive (2013, background): “Engineered overexpres‐ sion of biosynthetic enzymes for osmoprotectants such as glycine betaine [164,165]; stress induced proteins such as LEA proteins [166-167]; scavengers of reactive oxygen species [168,169]; transcription factors [170, 171] or signal transduction components [172-173] were report”
Role of DREBs in regulation of abiotic stress responses in plants. (2011, background): “genes, thus providing enhanced stress tolerance to plants (Shen et al., 2003a; Oh et al., 2005; Bhatnagar-Mathur et al., 2006; Sakuma et al., 2006a, b; Schramm et al., 2008).”
Understanding regulatory networks and engineering for enhanced drought tolerance in plants. (2006, background): “To compare the stress responses of Arabidopsis and rice, transgenic rice plants were developed that constitutively express CBF3/DREB1A (CBF3) and ABF3, Arabidopsis genes that function in ABA-independent and ABAdependent stress-response pathways, respectively [36].”
Cold stress regulation of gene expression in plants. (2007, background): “Transgenic analyses have shown that overexpression of Arabidopsis CBFs in chilling-sensitive plants such as tomato and rice enhances the chilling tolerance of these plants [73, 74 ].”
The transcriptional regulatory network in the drought response and its crosstalk in abiotic stress responses including drought, cold, and heat (2014, background): “…(Hong et al., 2006), peanut (Bhatnagar-Mathur et al., 2007, Bhatnagar-Mathur et al., 2013), potato (Behnam et al., 2007; Iwaki et al., 2013), rice (Oh et al., 2005; Ito et al., 2006; Datta et al., 2012), soybean (Polizel et al., 2011; de Paiva Rolla et al., 2013), tobacco (Kasuga et al., 2004),…”
Antibiotic resistance plasmids in wastewater treatment plants and their possible dissemination into the environment (2010, background): “Moreover, transgenic rice plants have shown elevated levels of tolerance to drought and high salt stresses, but very low level of tolerance to low temperature stress (Oh et al., 2005).”