Abstract:We previously reported that transgenic rice (Oryza sativa L.) lines overexpressing OsWRKY11 showed significant desiccation tolerance, as indicated by their slower water loss in detached leaves. Here we examined the contents of sucrose, glucose, fructose and raffinose. Raffinose was shown to accumulate at a significantly higher level in the transgenic plants overexpressing OsWRKY11. Microarray analysis of gene expression profile indicated that the gene expression of Os07g0209100 encoding raffinose synthase and … Show more
“…Overexpression of WRKY in rice induced expression of galactinol synthase and raffinose synthase genes and also improved drought tolerance [62]. Raffinose may play a protectant role in drying resurrection plants [64].…”
Section: Transcription Factors and The Aba Induction Pathway For Desimentioning
confidence: 99%
“…WRKY transcription factors (TFs) bind to the W box, TTGAC(C/T), in promoters of specific genes to activate their expression [62]. The WRKY TFs occur in developing seed and are key agents in the ABA regulatory pathways that respond to environmental stresses, senescence, dormancy and germination of seeds.…”
Section: Transcription Factors and The Aba Induction Pathway For Desimentioning
Abstract:The majority of flowering-plant species can survive complete air-dryness in their seed and/or pollen. Relatively few species ('resurrection plants') express this desiccation tolerance in their foliage. Knowledge of the regulation of desiccation tolerance in resurrection plant foliage is reviewed. Elucidation of the regulatory mechanism in resurrection grasses may lead to identification of genes that can improve stress tolerance and yield of major crop species. Well-hydrated leaves of resurrection plants are desiccation-sensitive and the leaves become desiccation tolerant as they are drying. Such drought-induction of desiccation tolerance involves changes in gene-expression causing extensive changes in the complement of proteins and the transition to a highly-stable quiescent state lasting months to years. These changes in gene-expression are regulated by several interacting phytohormones, of which drought-induced abscisic acid (ABA) is particularly important in some species. Treatment with only ABA induces desiccation tolerance in vegetative tissue of Borya constricta Churchill. and Craterostigma plantagineum Hochstetter. but not in the resurrection grass Sporobolus stapfianus Gandoger. Suppression of drought-induced senescence is also important for survival of drying. Further research is needed on the triggering of the induction of desiccation tolerance, on the transition between phases of protein synthesis and on the role of the phytohormone, strigolactone and other potential xylem-messengers during drying and rehydration.
“…Overexpression of WRKY in rice induced expression of galactinol synthase and raffinose synthase genes and also improved drought tolerance [62]. Raffinose may play a protectant role in drying resurrection plants [64].…”
Section: Transcription Factors and The Aba Induction Pathway For Desimentioning
confidence: 99%
“…WRKY transcription factors (TFs) bind to the W box, TTGAC(C/T), in promoters of specific genes to activate their expression [62]. The WRKY TFs occur in developing seed and are key agents in the ABA regulatory pathways that respond to environmental stresses, senescence, dormancy and germination of seeds.…”
Section: Transcription Factors and The Aba Induction Pathway For Desimentioning
Abstract:The majority of flowering-plant species can survive complete air-dryness in their seed and/or pollen. Relatively few species ('resurrection plants') express this desiccation tolerance in their foliage. Knowledge of the regulation of desiccation tolerance in resurrection plant foliage is reviewed. Elucidation of the regulatory mechanism in resurrection grasses may lead to identification of genes that can improve stress tolerance and yield of major crop species. Well-hydrated leaves of resurrection plants are desiccation-sensitive and the leaves become desiccation tolerant as they are drying. Such drought-induction of desiccation tolerance involves changes in gene-expression causing extensive changes in the complement of proteins and the transition to a highly-stable quiescent state lasting months to years. These changes in gene-expression are regulated by several interacting phytohormones, of which drought-induced abscisic acid (ABA) is particularly important in some species. Treatment with only ABA induces desiccation tolerance in vegetative tissue of Borya constricta Churchill. and Craterostigma plantagineum Hochstetter. but not in the resurrection grass Sporobolus stapfianus Gandoger. Suppression of drought-induced senescence is also important for survival of drying. Further research is needed on the triggering of the induction of desiccation tolerance, on the transition between phases of protein synthesis and on the role of the phytohormone, strigolactone and other potential xylem-messengers during drying and rehydration.
“…There have been many studies showing that the expression of genes related to biosynthesis of galactinol and raffinose is involved in several stresses, and expression specificity of the GolS genes to different stresses has also been reported in Arabidopsis. In rice, accumulation of raffinose in seedlings overexpressing OsWRKY11, which is related to heat shock and drought stress, was reported (Wu et al, 2009). It has also been reported that raffinose content in cold-tolerant rice was slightly increased by chilling treatment at 13/10 • C for 4 days (Morsy et al, 2007) and that the expression of a GolS homologous gene was induced in rice seedlings exposed to a Abbreviations: AGA, alkaline ␣-galactosidase; GolS, galactinol synthase; ORF, open reading frame; RFO, raffinose oligosaccharide; RS, raffinose synthase; SIP, seed imbibition protein.…”
“…The accumulation of galactinol and raffinose in vegetative tissues of different plant species occurs under cold, heat, drought and osmotic stresses (ElSayed et al 2014;Pastorczyk et al 2014). The concentrations of accumulated galactinol and/or raffinose can be sufficiently high to confirm the osmoprotective role of both galactosides (Sun et al 2013;Wang et al 2012a;Wu et al 2009). However, in dehydrated seedlings of wheat (Bogdan and Zagdańska 2006), winter vetch (Vicia villosa Roth) (Lahuta and Górecki 2011) and pea , the concentration of accumulated raffinose is very low.…”
The objective of the present study was to recognize the molecular background of the accumulation of raffinose family oligosaccharides (RFOs) in pea (Pisum sativum L.) seedlings under osmotic stress conditions. The exposure of 5-day-old pea seedlings to osmotic stress for 48 h created by immersing roots in PEG8000 solution (-1.5 MPa) induced synthesis of galactinol and RFOs (raffinose and stachyose) in the epicotyl and root tissues, but not in cotyledons. After 24 h of recovery, galactinol completely disappeared, raffinose decreased fourfold and stachyose decreased twofold in roots, but increased in epicotyls. The temporary accumulation of RFOs resulted from a dramatic increase in the enzymatic activity and changes in expression of galactinol synthase (PsGolS), raffinose synthase (PsRS) and stachyose synthase (PsSTS) genes. PsGolS was induced by osmotic stress in both epicotyls as well as in roots. PsRS and PsSTS were induced only in epicotyls, but repressed or remained unaffected in roots, respectively. During recovery, the expression and activity of PsGolS, PsRS and PsSTS dramatically decreased. The expression of PsGolS gene, that level of mRNA transcript significantly decreased during recovery and whose promoter region was identified to contain some stress-related regulating elements, seems to play a crucial role in the biosynthesis of RFOs under osmotic stress. Possible signals that may trigger the induction of expression of PsGolS, PsRS and PsSTS genes and accumulation of RFOs in pea seedlings are discussed.
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