Corominas M, Mezquita C
J Biol Chem. 1985 Dec 25;260(30):16269-73.
Rooster testis cells were separated by sedimentation at unit gravity and the in vivo levels of polymeric ADP-ribose were determined both in intact cells and isolated nuclei by fluorescence methods. Poly(ADP-ribose) polymerase activity was assayed after cell permeabilization or after isolation of nuclei. The turnover of ADP-ribosyl residues was determined in isolated nuclei using benzamide. The content of poly(ADP-ribose), the poly(ADP-ribose) polymerase activity, and the turnover of ADP-ribosyl residues, decreased during the differentiation of the germinal cell line, especially at the end of spermiogenesis. Treatment of cells with 1 mM dimethyl sulfate for 1 h resulted in a marked stimulation of poly(ADP-ribose) polymerase activity in meiotic and premeiotic cells and also in round and late spermatids. The enzymatic activity was not detected and could not be induced in mature spermatozoa. These cells, however, still contained polymeric ADP-ribose with a 2% of branched form.
通过单位重力沉降法分离公鸡睾丸细胞,并采用荧光法测定完整细胞和分离细胞核中多聚ADP - 核糖的体内水平。在细胞透化后或细胞核分离后测定多聚(ADP - 核糖)聚合酶活性。使用苯甲酰胺在分离的细胞核中测定ADP - 核糖基残基的周转率。在生殖细胞系分化过程中,尤其是在精子发生末期,多聚(ADP - 核糖)的含量、多聚(ADP - 核糖)聚合酶活性以及ADP - 核糖基残基的周转率均降低。用1 mM硫酸二甲酯处理细胞1小时,导致减数分裂和减数分裂前细胞以及圆形和晚期精子细胞中的多聚(ADP - 核糖)聚合酶活性显著增强。在成熟精子中未检测到该酶活性,也无法诱导其产生。然而,这些细胞仍含有2%分支形式的多聚ADP - 核糖。