Collatz E, Plesset J, Foy J J, McLaughlin C S
Department of Biological Chemistry, University of California, Irvine 92717.
Yeast. 1985 Sep;1(1):49-56. doi: 10.1002/yea.320010106.
Plasmid pPW229, containing the 2.25 kilobase transcribed sequence for the 70,000 Dalton heat shock protein of Drosophila, was integrated into plasmid CV13 and used to transform Saccharomyces cerevisiae. Upon a heat shock, at 41 degrees C for 20 min, a new 70,000 Dalton protein appeared in the transformants. This protein was not detected in transformants grown at 23 degrees C, nor in transformants carrying the hybrid plasmid from which the structural gene for the 70,000 Dalton protein had been deleted. RNA was isolated from transformants grown at 23 degrees C and from transformants heat shocked at 41 degrees C. RNA complementary to the Drosophila heat shock gene was present in the transformants, grown either at 23 degrees C or heat shocked. No complementary RNA was detected in yeast cells transformed with the hybrid plasmid from which the structural gene had been deleted. The Drosophila heat shock gene in yeast appears to be transcribed constitutively but translated only under heat shock conditions.
含有果蝇70000道尔顿热休克蛋白2.25千碱基转录序列的质粒pPW229,被整合到质粒CV13中,并用于转化酿酒酵母。在41℃热休克20分钟后,转化体中出现了一种新的70000道尔顿蛋白。在23℃生长的转化体中未检测到这种蛋白,在携带已缺失70000道尔顿蛋白结构基因的杂交质粒的转化体中也未检测到。从23℃生长的转化体和41℃热休克的转化体中分离RNA。与果蝇热休克基因互补的RNA存在于23℃生长或热休克的转化体中。在用已缺失结构基因的杂交质粒转化的酵母细胞中未检测到互补RNA。酵母中的果蝇热休克基因似乎是组成型转录的,但仅在热休克条件下才进行翻译。