Steinemann M
Chromosoma. 1976 Mar 10;54(4):339-48. doi: 10.1007/BF00292814.
The DNA of Drosophila virilis brains and imaginal discs was labeled in vitro to a specific activity of 6 X 10(-5) dpm/mug, using an organ culture medium. The DNA was fractionated on neutral and alkaline CsC1 gradients and the heavy strands of satellite I annealed in situ to denatured polytene chromosomes from squash preparations of larval salivary glands. Nuclease S1 from Aspergillus oryzae was used to digest the unpaired ssDNA, resulting in a distinct labeling of the alpha-heterochromatin in the chromocenter and a small amount of diffused labeling in the proximal beta-heterochromatic part of the X-Chromsome.
使用器官培养基在体外将果蝇大脑和成虫盘的DNA标记至比活度为6×10⁻⁵ dpm/μg。将DNA在中性和碱性CsCl梯度上进行分级分离,卫星I的重链原位退火至来自幼虫唾液腺压片制备的变性多线染色体。使用米曲霉的核酸酶S1消化未配对的单链DNA,导致染色中心的α-异染色质有明显标记,并且在X染色体近端β-异染色质部分有少量弥散标记。