Evgen'ev M B, Kolchinski A, Levin A, Preobrazhenskaya A L, Sarkisova E
Chromosoma. 1978 Sep 11;68(4):357-65. doi: 10.1007/BF00327170.
Polytene chromosomes of D. melanogaster and D. virilis were hybridized in situ with 125I labeled mRNA isolated from polysomes of D. melanogaster tissue culture cells incubated at 37 degrees C. 125I mRNA hybridized preferentially with subdivisions 87A and 87Cl of the D. melanogaster 3R chromosome; grains were also observed at regions 93D, 95D and over the chromocenter. A considerable cross hybridization of this mRNA with D. virilis polytene chromosomes was observed. The 29C region of the D. virilis second chromosome was the main site of hybridization. Significant grain numbers also appeared in region 20F of the same chromosome. The two regions mentioned belong to heat shock loci in the latter species. Based on label intensity we conclude that region 29C of D. virilis contains DNA sequences retaining molecular homology with those at subdivisions 87A and 87Cl of D. melanogaster. SDS-polyacrylamide gel electrophoresis revealed similar distributions of heat shock proteins in the two species studied.
将黑腹果蝇和拟果蝇的多线染色体与从在37℃下培养的黑腹果蝇组织培养细胞的多核糖体中分离出的125I标记的mRNA进行原位杂交。125I mRNA优先与黑腹果蝇3R染色体的87A和87Cl亚区杂交;在93D、95D区域以及染色中心也观察到了银粒。观察到这种mRNA与拟果蝇多线染色体有相当程度的交叉杂交。拟果蝇第二条染色体的29C区域是主要杂交位点。在同一条染色体的20F区域也出现了大量银粒。上述两个区域属于后一种果蝇的热休克基因座。根据标记强度,我们得出结论,拟果蝇的29C区域包含与黑腹果蝇87A和87Cl亚区的DNA序列保持分子同源性的DNA序列。SDS-聚丙烯酰胺凝胶电泳显示,在所研究的两个物种中热休克蛋白的分布相似。