Hoober J K, Stegeman W J
J Cell Biol. 1976 Aug;70(2 pt 1):326-37. doi: 10.1083/jcb.70.2.326.
Etiolated cells of Chlamydomonas reinhardtii y-1 exhibit rapid and linear initial kinetics of greening when exposed to light at 38 degrees C. The initial rate of chlorophyll accumulation under these conditions is greater than the maximal rate during greening at 25 degrees C. Synthesis of the major polypeptides of thylakoid membranes within intact cells was assayed during greening by the incorporation of [3H]leucine and the subsequent electrophoresis of total cellular protein on polyacrylamide gels in the presence of sodium dodecyl sulfate. At 38 degrees C the major membrane polypeptides (about 28,000 and 24,000 daltons in mass) were synthesized at a linear rate after exposure of the cells to light, with no evidence of a lag period. A 1-2 h preincubation in the dark at the higher temperature was necessary to achieve linear initial kinetics. Actinomycin D inhibited synthesis of the membrane polypeptides if added at the beginning of a 2 h dark preincubation, but not when added near the end. These results suggested that transcription of the messenger RNA for the membrane polypeptides occurred during the dark period at 38 degrees C. But the major membrane polypeptides were not made by y-1 cells in the dark. The wavelengths of light most effective in eliciting production of the membrane polypeptides were the same as those allowing chlorophyll synthesis. In contrast, wild type cells, which are capable of chlorophyll synthesis in the dark, also make the membrane polypeptides in the dark. The data indicate that at elevated temperatures synthesis of the major thylakoid membrane polypeptides is controlled at a posttranscriptional step, and that this reaction normally proceeds only under conditions which permit reduction of protochlorophyllide.
莱茵衣藻y-1的黄化细胞在38摄氏度光照下呈现出快速且线性的初始变绿动力学。在这些条件下叶绿素积累的初始速率大于25摄氏度变绿过程中的最大速率。在变绿过程中,通过掺入[3H]亮氨酸并随后在十二烷基硫酸钠存在下对总细胞蛋白进行聚丙烯酰胺凝胶电泳,来检测完整细胞内类囊体膜主要多肽的合成。在38摄氏度时,细胞暴露于光照后,主要膜多肽(质量约为28,000和24,000道尔顿)以线性速率合成,没有延迟期的迹象。在较高温度下黑暗中预孵育1 - 2小时对于实现线性初始动力学是必要的。如果在2小时黑暗预孵育开始时加入放线菌素D,则会抑制膜多肽的合成,但在接近结束时加入则不会。这些结果表明,膜多肽信使RNA的转录发生在38摄氏度的黑暗期。但y-1细胞在黑暗中不合成主要膜多肽。最有效地引发膜多肽产生的光波长与允许叶绿素合成的光波长相同。相比之下,能够在黑暗中合成叶绿素的野生型细胞在黑暗中也能合成膜多肽。数据表明,在升高的温度下,主要类囊体膜多肽的合成在转录后步骤受到控制,并且该反应通常仅在允许原叶绿素酸酯还原的条件下进行。