Answers are grounded in this paper and cite their sources.
The role of gibberellins (GAs) in photoperiodic control of leaf elongation in Poa pratensis was studied by both application of exogenous GAs and analysis of endogenous GAs. Leaf elongation was strongly increased under long day (LD, 24 h) conditions at both 9 and 21°C, leaf length at 9°C LD being similar to that in plants grown in short days (SD, 8 h) at 21°C. However, even at 21°C leaf elongation was enhanced by LD. Exogenous GA 1 could completely compensate for LD at both 9 and 21°C. Gibberellins A 20 , A 19 and A 44 could also partly replace LD, but they were significantly less active than GA 1 , GA 53 was inactive when applied to plants grown at 9°C in SD and exhibited only marginal activity at 9°C LD and 21°C SD. The total level of GAs of the early 13‐hydroxylation pathway (A 53 , A 44 , A 19 , A 20 and A 1 ) increased rapidly when plants were transferred from SD to LD at 9°C. After transfer from 9 to 21°C, there was an increase in GA levels at both LD and SD, followed by a decrease under LD conditions. In all cases, GA 19 was the predominant GA, accounting for 60 to 80% of the analysed GAs. Levels of the bioactive GA 1 were low and increased transiently by LD four days after transfer from SD to LD. At both temperatures, the ratio GA 19 to GA 20 and GA 20 to GA 1 at 9°C was enhanced by LD compared with SD. Taken together, these results support the hypothesis that photoperiodic regulation of leaf elongation in Poa pratensis is GA‐mediated, and they indicate a photoperiodic control of oxidation of GA 53 to GA 44 and GA 19 to GA 20 , and perhaps also of 3β‐hydroxylation of GA 20 to GA 1 .
No takes yet. Share an insight, caveat, or question.
Junttila et al. (1997) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: