Department of Biological Sciences, Stanford University, Stanford, California 94305-5020.
Plant Physiol. 1988 Dec;88(4):965-8. doi: 10.1104/pp.88.4.965.
The response of maize (Zea mays L.) protoplasts to high temperature stress was investigated. After isolation and electroporation, protoplasts were preincubated for 12 hours at 26 degrees C then incubated for 6 hours at elevated temperatures. The pattern of polypeptides synthesized by these protoplasts during the last hour was monitored by in vivo labeling with (35)S-methionine. Incubation at 40 degrees and 42 degrees C resulted in the synthesis of polypeptides not detectable at 26 degrees C. Introduction of a chimeric maize heat shock protein 70 promoter-chloramphenicol acetyltransferase coding region gene into protoplasts via electroporation resulted in the temperature-dependent induction of chloramphenicol acetyltransferase activity with maximal activity at 40 degrees C. In the same protoplasts, a second chimeric gene, in which the firefly luciferase coding region was under the control of the 35S promoter from cauliflower mosaic virus, did not show an increase in expression after incubation at higher temperatures. Maize protoplasts provide a system to study molecular responses to high temperature stress.
研究了玉米(Zea mays L.)原生质体对高温胁迫的反应。分离和电穿孔后,原生质体在 26°C 下预培养 12 小时,然后在高温下孵育 6 小时。在最后 1 小时内,通过用(35)S-甲硫氨酸进行体内标记监测这些原生质体合成的多肽。在 40°C 和 42°C 下孵育导致在 26°C 下不可检测的多肽的合成。通过电穿孔将嵌合玉米热激蛋白 70 启动子-氯霉素乙酰转移酶编码区基因引入原生质体,导致氯霉素乙酰转移酶活性在 40°C 时呈现温度依赖性诱导,最大活性在 40°C 时。在相同的原生质体中,第二个嵌合基因,其中萤火虫荧光素酶编码区受花椰菜花叶病毒 35S 启动子的控制,在高温孵育后其表达没有增加。玉米原生质体提供了一种研究分子对高温胁迫反应的系统。