Lewis M, Helmsing P J, Ashburner M
Proc Natl Acad Sci U S A. 1975 Sep;72(9):3604-8. doi: 10.1073/pnas.72.9.3604.
The changes in protein synthesis of salivary glands of Drosophila resulting from a brief exposure at 37 degrees have been analyzed on sodium dodecyl sulfate--acrylamide gels. In D. melanogaster and D. hydei this treatment induces nine and six new puffs, respectively, in the polytene chromosomes. After 20 min treatment seven new proteins are synthesized by the glands of D. melanogaster and six by those of D. hydei as detected by [35S]methionine labeling. Other agents, e.g., recovery from anaerobiosis, induce the same puffs and the same proteins. The extent of protein induction and the degree of puff induction are related to the severity of the temperature treatment. The new proteins are detected after 10 min treatmene at 37 degrees and their synthesis is inhibited by actinomycin D. Actinomycin D added 5 min after the start of temperature treatment has little effect on subsequent protein synthesis. The induced proteins are not tissue specific. Electrophoretic differences of two proteins exist between D. melanogaster and D. simulans, encouraging attempts to map the proteins' gene loci and to test directly whether or not the puffs code for them.
利用十二烷基硫酸钠-丙烯酰胺凝胶对经37℃短暂处理的果蝇唾液腺蛋白质合成变化进行了分析。在黑腹果蝇和海德氏果蝇中,这种处理分别在多线染色体上诱导出9个和6个新的胀泡。经[35S]甲硫氨酸标记检测,处理20分钟后,黑腹果蝇的唾液腺合成了7种新蛋白质,海德氏果蝇的唾液腺合成了6种新蛋白质。其他因素,如从厌氧状态恢复,也会诱导相同的胀泡和相同的蛋白质。蛋白质诱导程度和胀泡诱导程度与温度处理的强度有关。在37℃处理10分钟后可检测到新蛋白质,其合成受放线菌素D抑制。在温度处理开始5分钟后加入放线菌素D对随后的蛋白质合成影响很小。诱导产生的蛋白质不是组织特异性的。黑腹果蝇和拟暗果蝇之间两种蛋白质存在电泳差异,这促使人们尝试对蛋白质的基因座进行定位,并直接测试胀泡是否编码这些蛋白质。