1992
DOI: 10.1104/pp.99.4.1664
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Regulation of Phosphoenolpyruvate Carboxylase and Crassulacean Acid Metabolism Induction in Mesembryanthemum crystallinum L. by Cytokinin

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Cited by 63 publications
(41 citation statements)
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“…Other plant growth regulators such as cytokinins have been shown to either suppress or enhance PEPC expression depending on the mode of application (Schmitt and Piepenbrock, 1992;Thomas et al, 1992;Thomas and Bohnert, 1993;Dai et al, 1994;Peters et al, 1997). Cytokinin applied to roots causes an enhancement in PEPC expression, whereas foliar application of intact plants or feeding to detached leaves suppresses PEPC expression and prevents PEPC induction by drought or salinity stress (Schmitt and Piepenbrock, 1992;Dai et al, 1994;Peters et al, 1997). Endogenous cytokinin levels are negatively correlated with Ppc1 transcripts during dehydration stress, suggesting that cytokinins act as negative effectors in the expression of CAM (Peters et al, 1997).…”
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confidence: 99%
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“…Other plant growth regulators such as cytokinins have been shown to either suppress or enhance PEPC expression depending on the mode of application (Schmitt and Piepenbrock, 1992;Thomas et al, 1992;Thomas and Bohnert, 1993;Dai et al, 1994;Peters et al, 1997). Cytokinin applied to roots causes an enhancement in PEPC expression, whereas foliar application of intact plants or feeding to detached leaves suppresses PEPC expression and prevents PEPC induction by drought or salinity stress (Schmitt and Piepenbrock, 1992;Dai et al, 1994;Peters et al, 1997). Endogenous cytokinin levels are negatively correlated with Ppc1 transcripts during dehydration stress, suggesting that cytokinins act as negative effectors in the expression of CAM (Peters et al, 1997).…”
mentioning
confidence: 99%
“…Endogenous increases or exogenous application of ABA result in CAM induction (Dai et al, 1994;Taybi et al, 1995) by stimulating increased expression of key CAM enzymes such as PEPC (Chu et al, 1990;Dai et al, 1994;Taybi et al, 1995), enolase (Forsthoefel et al, 1995a), phosphoglyceromutase (Forsthoefel et al, 1995b), and vacuolar ATPase subunit c (Tsiantis et al, 1996). Other plant growth regulators such as cytokinins have been shown to either suppress or enhance PEPC expression depending on the mode of application (Schmitt and Piepenbrock, 1992;Thomas et al, 1992;Thomas and Bohnert, 1993;Dai et al, 1994;Peters et al, 1997). Cytokinin applied to roots causes an enhancement in PEPC expression, whereas foliar application of intact plants or feeding to detached leaves suppresses PEPC expression and prevents PEPC induction by drought or salinity stress (Schmitt and Piepenbrock, 1992;Dai et al, 1994;Peters et al, 1997).…”
mentioning
confidence: 99%
“…Despite the changes in leaf water content seen in C3-type plants, changes in PEPCase mRNA abundance are not observed (Schmitt & Piepenbrock 1992). These data imply that the induction of PEPCase might be suppressed hy a signal originating from outside the leaf (Schmitt & Piepenbrock 1992).…”
Section: Discussionmentioning
confidence: 72%
“…Interestingly, exogenously applied ABA and eytokinin have also been shown to influence CAM expression in M. crystaltittiim (Chu et at. 1990;Schmitt & Piepenbrock 1992;Thomas et al 1992). The possible involvement of these growth regulators in CAM induction has lead a number of authors to speculate that they might act as root-derived messengers, modulating the expression of the CAM pathway in response lo changing lool water status Schmitt & Piepenbrock 1992;Thomas & Bohnert 1993).…”
Section: Introductionmentioning
confidence: 99%
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