1996
DOI: 10.1007/bf01979922
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Expression of the isopentenyl transferase gene is regulated by auxin in transgenic tobacco tissues

Abstract: The isopentenyl transferase gene (ipt) from Agrobacterium tumefaciens was isolated and introduced, via a disarmed binary vector, into tobacco using the Agrobacterium tumefaciens-mediated gene transfer system. The expression of the ipt gene was monitored by RNA hybridization, western blotting and cytokinin analysis. The addition of auxin to the media rapidly reduced the level of cytokinins in the transgenic tissues and this was associated with a reduction in IPT mRNA and protein levels. It is concluded that the… Show more

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Cited by 21 publications
(6 citation statements)
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References 46 publications
(54 reference statements)
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“…Regenerated shoots at first did not form roots and were devoid of apical domination, a fact that was also reported by others [46][47][48]. As reported by Zhang and co-workers, [49], the expression of isopentyl transferase in transgenic tobacco plants may be controlled by auxins. We have therefore used exogenous auxin and this allowed us to obtain normal transgenic plants having an intermediate level of cytokinine in comparison with normal transgenic plants and the crown gall tissue [50].…”
Section: An Experimental Model For Studying the Role Of Isopentyl Trasupporting
confidence: 64%
“…Regenerated shoots at first did not form roots and were devoid of apical domination, a fact that was also reported by others [46][47][48]. As reported by Zhang and co-workers, [49], the expression of isopentyl transferase in transgenic tobacco plants may be controlled by auxins. We have therefore used exogenous auxin and this allowed us to obtain normal transgenic plants having an intermediate level of cytokinine in comparison with normal transgenic plants and the crown gall tissue [50].…”
Section: An Experimental Model For Studying the Role Of Isopentyl Trasupporting
confidence: 64%
“…The phenotypes of Mt CRE1 RNAi roots are consistent with a general role for cytokinins in the control of the initiation of lateral root organs and more generally on the control of root architecture in response to environmental conditions and root apical dominance (Franco-Zorrilla et al, 2002;Aloni et al, 2006). It is well known that a primary target of cytokinin action is cell cycle control (Redig et al, 1996;Zhang et al, 1996). Our results from Mt CRE1-silenced roots could be integrated by proposing that reduced nodulation may rely on a block of cortical cell divisions, whereas increased lateral root formation may be related to an activation of pericycle divisions.…”
Section: Discussionmentioning
confidence: 56%
“…Our previous study using cytokinin-overproducing tobacco plants revealed a strong increase in CKX activity as a consequence of elevated cytokinin levels (Motyka et al 1996;Motyka et al 2003). Stimulation of CKX activity by endogenous or externally applied (both substrate and non-substrate) cytokinins has also been reported in other plants and plant cultures (Chatfield and Armstrong 1986;Kamı´nek and Armstrong 1990;Motyka and Kamı´nek 1990;Zhang et al 1996;Auer et al 1999). It is evident that BA, which is intensively glucosylated (data not shown), is capable of stimulating both metabolic processes, i.e., N-glucosylation and oxidative breakdown.…”
Section: The Effect Of Exogenous Cytokinins On Cytokinin 7n-glucosylamentioning
confidence: 86%