Grippo P, Cossu G, Molinaro M
Cell Differ. 1977 Jun;6(1):9-16. doi: 10.1016/0045-6039(77)90040-9.
DNA-dependent DNA polymerases have been studied during chick embryo muscle differentiation in vitro. The total activity, extracted at both low and high ionic strengths, does not change throughout the differentiative process, although DNA synthesis stops at the moment of fusion. Analyses by glycerol gradient centrifugation of the extracts at low and high ionic strengths show two major DNA polymerase forms, one sedimenting at 7.5 S and another at 3-4 S. Both enzymes are present in similar amounts in duplicating myoblasts and in post-mitotic myotubes. These data suggest that the arrest of DNA synthesis which accompanies myoblast differentiation is not dependent on the disappearance or decrease of the major DNA polymerase activities described.
已在体外鸡胚肌肉分化过程中对依赖DNA的DNA聚合酶进行了研究。在低离子强度和高离子强度下提取的总活性,在整个分化过程中都没有变化,尽管DNA合成在融合时停止。对低离子强度和高离子强度提取物进行甘油梯度离心分析,显示出两种主要的DNA聚合酶形式,一种在7.5 S沉降,另一种在3 - 4 S沉降。这两种酶在复制的成肌细胞和有丝分裂后的肌管中的含量相似。这些数据表明,伴随成肌细胞分化的DNA合成停滞并不依赖于所述主要DNA聚合酶活性的消失或降低。