Gibberellins （GAs） cause dramatic increases in plant height and a genetic block in the synthesis of GA1 explains the dwarfing of Mendel＇s pea. For flowering, it is GAs which is important in the long-day （LD） resp...Gibberellins （GAs） cause dramatic increases in plant height and a genetic block in the synthesis of GA1 explains the dwarfing of Mendel＇s pea. For flowering, it is GAs which is important in the long-day （LD） responsive grass, Loliurn. As we show here, GA1 and GA4 are restricted in their effectiveness for flowering because they are deactivated by C-2 hydroxylation below the shoot apex. In contrast, GAs is effective because of its structural protection at C-2. Excised vegetative shoot tips rapidly degrade [14C]GA1, [14C]GA4, and [14C]GA20 （〉80% in 6 h）, but not [14C]GAs. CoincidentaUy, genes encoding two 2β-oxidases and a putative 16-17-epoxidase were most expressed just below the shoot apex （〈3 mm）. Further down the immature stem （〉4 mm）, expression of these GA deactivation genes is reduced, so allowing GA1 and GA4 to promote sub-apical stem elongation. Subsequently, GA degradation declines in florally induced shoot tips and these GAs can become active for floral development. Structural changes which stabilize GA4 confirm the link between florigenicity and restricted GA 2β-hydroxylation （e.g. 2α-hydroxylation and C-2 di-methylation）. Additionally, a 2-oxidase inhibitor （Trinexapac Ethyl） enhanced the activity of applied GA4, as did limiting C-16,17 epoxidation in 16,17-dihydro GAs or after C-13 hydroxylation. Overall, deactivation of GA1 and GA4 just below the shoot apex effectively restricts their florigenicity in Loliurn and, conversely, with GAs, C-2 and C-13 protection against deactivation allows its high florigenicity. Speculatively, such differences in GA access to the shoot apex of grasses may be important for separating floral induction from inflorescence emergence and thus could influence their survival under conditions of herbivore predation.展开更多
文摘Gibberellins （GAs） cause dramatic increases in plant height and a genetic block in the synthesis of GA1 explains the dwarfing of Mendel＇s pea. For flowering, it is GAs which is important in the long-day （LD） responsive grass, Loliurn. As we show here, GA1 and GA4 are restricted in their effectiveness for flowering because they are deactivated by C-2 hydroxylation below the shoot apex. In contrast, GAs is effective because of its structural protection at C-2. Excised vegetative shoot tips rapidly degrade [14C]GA1, [14C]GA4, and [14C]GA20 （〉80% in 6 h）, but not [14C]GAs. CoincidentaUy, genes encoding two 2β-oxidases and a putative 16-17-epoxidase were most expressed just below the shoot apex （〈3 mm）. Further down the immature stem （〉4 mm）, expression of these GA deactivation genes is reduced, so allowing GA1 and GA4 to promote sub-apical stem elongation. Subsequently, GA degradation declines in florally induced shoot tips and these GAs can become active for floral development. Structural changes which stabilize GA4 confirm the link between florigenicity and restricted GA 2β-hydroxylation （e.g. 2α-hydroxylation and C-2 di-methylation）. Additionally, a 2-oxidase inhibitor （Trinexapac Ethyl） enhanced the activity of applied GA4, as did limiting C-16,17 epoxidation in 16,17-dihydro GAs or after C-13 hydroxylation. Overall, deactivation of GA1 and GA4 just below the shoot apex effectively restricts their florigenicity in Loliurn and, conversely, with GAs, C-2 and C-13 protection against deactivation allows its high florigenicity. Speculatively, such differences in GA access to the shoot apex of grasses may be important for separating floral induction from inflorescence emergence and thus could influence their survival under conditions of herbivore predation.
