Adlakha R C, Sahasrabuddhe C G, Wright D A, Lindsey W F, Smith M L, Rao P N
Nucleic Acids Res. 1982 Jul 10;10(13):4107-17. doi: 10.1093/nar/10.13.4107.
Additional evidence is presented to support our recently reported conclusion that the mitotic factors of mammalian cells, which induce germinal vesicle breakdown and chromosome condensation when injected into fully grown Xenopus laevis oocytes, are localized on metaphase chromosomes. Chromosomes isolated from mitotic HeLa cells were further purified on sucrose gradients and digested for varying periods with either the micrococcal nuclease or DNase II. At each time point of digestion the amount of mitotic factors released was determined by injecting a supernatant of these fractions, obtained by high-speed centrifugation, into oocytes. The amount of DNA rendered acid soluble under the conditions of digestion used was 3% ot 5% of the total chromosomal DNA. The extent of release of mitotic factors with both nucleases was estimated to be about 30% to 40% as evidenced by the reextraction of the undigested chromosomal pellet with 0.2 M NaC1. Similar results were obtained when nuclei from G2 cells were digested under identical conditions. The release of these chromosome-bound mitotic factors by mild digestion with these nucleases though only partial, clearly demonstrates that a significant proportion of these factors are localized on metaphase chromosomes.
更多证据被提出来支持我们最近报道的结论,即当注射到完全成熟的非洲爪蟾卵母细胞中时能诱导生发泡破裂和染色体浓缩的哺乳动物细胞有丝分裂因子,定位于中期染色体上。从有丝分裂的HeLa细胞中分离出的染色体在蔗糖梯度上进一步纯化,并用微球菌核酸酶或DNase II消化不同时间。在每个消化时间点,通过将这些经高速离心获得的组分的上清液注射到卵母细胞中来测定释放的有丝分裂因子的量。在所使用的消化条件下变为酸溶性的DNA量为总染色体DNA的3%至5%。用两种核酸酶处理时,有丝分裂因子的释放程度估计约为30%至40%,用0.2M NaCl对未消化的染色体沉淀进行再提取证明了这一点。当在相同条件下消化G2期细胞的细胞核时,也获得了类似的结果。用这些核酸酶进行温和消化,虽然只是部分地释放了这些与染色体结合的有丝分裂因子,但清楚地表明这些因子中有很大一部分定位于中期染色体上。