The error bars correspond to the standard deviation (n = 3). The Pifithrin �� negative values on the y-axis denote decreases relative to the control. mm: mature transcript, am: alternative transcript. After validating the experimental approach, we characterized the effect

of glucose on the expression of the crtYB, crtI and crtS genes. The mRNA Eltanexor ic50 levels of the three carotenogenic genes decreased considerably upon the addition of glucose. In the case of the crtYB gene (Figure 1b), both the mature and the alternative transcripts reached minimum levels 4 h after the addition of glucose and returned to basal levels within 24 h. Curiously, the effect of glucose was significantly greater on the alternative messenger (~18-fold decrease) than on the mature messenger (~6-fold decrease). AZD7762 mw This result is striking, considering that both messengers are transcribed from the same promoter. A similar effect occurred with the crtI gene (Figure 1c); glucose decreased the levels of the alternative mRNA (~35-fold decrease) to a greater extent than the mature mRNA (~6-fold decrease). The repression effect disappeared quickly for both transcripts and was not detectable 24 h after the addition of glucose. In the case of the crtS gene (Figure 1d), glucose had a smaller effect, with an approximately 5-fold decrease in the mRNA levels at 2 h

after treatment. Interestingly, 24 h after adding the sugar, expression of the crtS gene was increased 10-fold. Depletion of the glucose added to the medium and the subsequent decrease of the repression effect caused by glucose may be responsible for the quick return of the mRNAs to their basal levels. To evaluate this possibility, we determined the amount of glucose remaining throughout the 24-h-period during which the expression response was observed (Figure 2a). The results indicated that the kinetics of glucose consumption were much slower than the return of the mRNAs to their basal levels. For most of the genes studied,

the glucose response (20 g/l final concentration) occurred mainly during the first 6 h after treatment. However, during that time frame, only 20% of the glucose was consumed, Masitinib (AB1010) with approximately 16 g/l remaining in the medium. Given this observation, we next determined whether lower concentrations of glucose were capable of generating a repression response. We determined the relative expression of the carotenogenesis genes after adding glucose to final concentrations of 10, 5 and 1 g/l. For all of the genes assayed (Figure 2b, only data for crtS is shown as an example), we observed that the maximum repression effect increased as the glucose concentration was increased. However, the response kinetics was practically identical for all of the glucose concentrations analyzed.