Okoloko G E, Lewis L N, Reid B R
Departments of Plant Science and Biochemistry, University of California, Riverside, California 92502.
Plant Physiol. 1970 Nov;46(5):660-5. doi: 10.1104/pp.46.5.660.
Red light, which produces the physiologically active form of phytochrome (Pfr), inhibited epicotyl elongation in intact dark-grown Alaska pea seedlings. This red light response was detectable 3 hours after the light treatment and became pronounced after 5 hours. The growth inhibition was completely reversed by far red light applied immediately after the red or by pretreatment of the seedlings with the plant hormone gibberellin A(3).Comparison of the total (32)P-labeled nucleic acids from control and red light-treated Alaska pea epicotyls on methylated albumin-kieselguhr columns revealed a marked alteration of the pattern of nucleic acid synthesis in this plant material with little or no effect on total isotope incorporation into nucleic acids. A single 5-minute red light perturbation caused a 2-fold stimulation of (32)P incorporation into the tRNA fraction while, simultaneously, (32)P incorporation into tenaciously bound RNA was reduced to 50% of control levels. Red light treatment had no effect on (32)P incorporation into the DNA-RNA, rRNA, or mRNA fractions. Far red light reversed the effect of red light on tRNA synthesis but did not restore tenaciously bound RNA levels to the control value. Gibberellin A(3) treatment did not cause reversal of any of the red light effects on RNA synthesis.These light-induced changes in nucleic acids were measurable before any changes in the physiological response (epicotyl elongation) could be detected. These results are consistent with a phytochrome-mediated differential gene activation mechanism in the Alaska pea epicotyl elongation system.
产生生理活性形式的光敏色素(Pfr)的红光,抑制了完整的、在黑暗中生长的阿拉斯加豌豆幼苗的上胚轴伸长。这种红光反应在光照处理3小时后即可检测到,5小时后变得明显。在红光照射后立即施加远红光,或用植物激素赤霉素A(3)对幼苗进行预处理,均可完全逆转生长抑制。在甲基化白蛋白-硅藻土柱上对对照和红光处理的阿拉斯加豌豆上胚轴的总(32)P标记核酸进行比较,结果显示这种植物材料中核酸合成模式发生了显著变化,而对核酸中总同位素掺入量的影响很小或没有影响。单次5分钟的红光干扰导致(32)P掺入tRNA组分的量增加了2倍,同时,(32)P掺入紧密结合RNA的量减少到对照水平的50%。红光处理对(32)P掺入DNA-RNA、rRNA或mRNA组分没有影响。远红光逆转了红光对tRNA合成的影响,但没有将紧密结合RNA的水平恢复到对照值。赤霉素A(3)处理并未逆转红光对RNA合成的任何影响。在检测到生理反应(上胚轴伸长)的任何变化之前,就可以测量到这些光诱导的核酸变化。这些结果与阿拉斯加豌豆上胚轴伸长系统中光敏色素介导的差异基因激活机制一致。