Fig. 6.
Expression of GPT2 during early seedling development on glucose. Seeds were sterilized, stratified, sown and transferred to light as for seedling development assays, with the inclusion of 4 % glucose or PEG-8000 of the equivalent osmotic potential to the medium. GPT2 expression was examined in seedlings after transfer to light, with samples of 200–250 seedlings flash-frozen in liquid nitrogen at the end of each photoperiod. Frozen seedlings were stored at −80 °C. Fold changes shown were calculated relative to levels of ACT2 expression and are displayed relative to the expression level on half-strength MS at each time point. Shaded areas represent dark periods and unshaded areas represent photoperiods. Data expressed relative to UBC are qualitatively identical. Error bars represent ±1 s.e. Plants grown on half-strength MS only, grown on half-strength MS with PEG-8000 with an equivalent osmotic potential to 4 % glucose, and grown on half-strength MS with 4 % glucose are as indicated in the key.

Expression of GPT2 during early seedling development on glucose. Seeds were sterilized, stratified, sown and transferred to light as for seedling development assays, with the inclusion of 4 % glucose or PEG-8000 of the equivalent osmotic potential to the medium. GPT2 expression was examined in seedlings after transfer to light, with samples of 200–250 seedlings flash-frozen in liquid nitrogen at the end of each photoperiod. Frozen seedlings were stored at −80 °C. Fold changes shown were calculated relative to levels of ACT2 expression and are displayed relative to the expression level on half-strength MS at each time point. Shaded areas represent dark periods and unshaded areas represent photoperiods. Data expressed relative to UBC are qualitatively identical. Error bars represent ±1 s.e. Plants grown on half-strength MS only, grown on half-strength MS with PEG-8000 with an equivalent osmotic potential to 4 % glucose, and grown on half-strength MS with 4 % glucose are as indicated in the key.

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