Skadsen R W, Scandalios J G
Proc Natl Acad Sci U S A. 1987 May;84(9):2785-9. doi: 10.1073/pnas.84.9.2785.
In dark-grown leaves of Zea mays, the catalase (H2O2:H2O2 oxidoreductase; EC 1.11.1.6; CAT) isozyme CAT-2 is absent. With continuous white light, CAT-2 protein levels increase (due to de novo synthesis) and plateau after 24 hr. When total poly(A)+ RNA (mRNA), polysomes, or isolated polysomal mRNA from light- and dark-treated leaves was translated in vitro, CAT-2 was detected only among the light-treated leaf products. A Cat2 clone was used to probe blots of total mRNA and polysomal mRNA from light- and dark-treated leaves. Cat2 mRNA was found in approximately equal quantities in both. Cat2 mRNA was equally distributed in identical high molecular weight fractions in polysomes from light- and dark-treated leaves and, therefore, was probably not sequestered in ribonucleoprotein particles in dark-grown leaves. The control of Cat2 expression appears to involve a unique form of translational inhibition in dark-grown leaves, preventing translation of the isolated mRNA and preventing polypeptide elongation. These results may have important implication in studies of translational control in other systems.
在黑暗中生长的玉米叶片中,过氧化氢酶(H2O2:H2O2氧化还原酶;EC 1.11.1.6;CAT)同工酶CAT-2不存在。在持续白光照射下,CAT-2蛋白质水平升高(由于从头合成),并在24小时后达到稳定状态。当来自光照和黑暗处理叶片的总聚腺苷酸加尾RNA(mRNA)、多核糖体或分离的多核糖体mRNA在体外进行翻译时,仅在光照处理的叶片产物中检测到CAT-2。使用Cat2克隆对光照和黑暗处理叶片的总mRNA和多核糖体mRNA印迹进行探针检测。发现Cat2 mRNA在两者中的含量大致相等。Cat2 mRNA在光照和黑暗处理叶片的多核糖体中以相同的高分子量级分均匀分布,因此,可能不会在黑暗生长叶片的核糖核蛋白颗粒中被隔离。Cat2表达的调控似乎涉及黑暗生长叶片中一种独特的翻译抑制形式,阻止分离的mRNA翻译并阻止多肽延伸。这些结果可能对其他系统的翻译调控研究具有重要意义。