Signoret J, Thiebaud P, Lefresne J, David J C
Dev Biol. 1986 Jul;116(1):8-14. doi: 10.1016/0012-1606(86)90037-0.
A change in the molecular form of DNA ligase appears when the sea urchin egg enters cleavage. Sucrose gradient analysis and DNA cellulose chromatography show that a slower migrating form (7 S) of enzyme exists in unfertilized eggs and in sperm. A faster migrating form of DNA ligase (7.8 S) is present in developing embryos as well as in artificially activated eggs. The timing of this early biochemical event has been determined, following fertilization or activation. The change in molecular form of DNA ligase has been shown to be sensitive to drugs inhibiting protein synthesis, gene transcription, or DNA replication. Consequently the appearance of the faster migrating form of enzyme is assumed to result from expression of the corresponding gene, transcription, and translation. RNA extracted from testes and from cleaving stages, assayed in vitro and in vivo, have been shown to carry the information for, respectively, 7 S and 7.8 S DNA ligase according to the origin of the RNA.
海胆卵进入卵裂期时,DNA连接酶的分子形式会发生变化。蔗糖梯度分析和DNA纤维素色谱法表明,未受精卵和精子中存在迁移速度较慢的酶形式(7S)。发育中的胚胎以及人工激活的卵中存在迁移速度较快的DNA连接酶形式(7.8S)。在受精或激活后,已确定了这一早期生化事件的时间。已证明DNA连接酶分子形式的变化对抑制蛋白质合成、基因转录或DNA复制的药物敏感。因此,假定迁移速度较快的酶形式的出现是相应基因表达、转录和翻译的结果。从睾丸和卵裂期提取的RNA,经体外和体内检测,根据RNA的来源,已证明分别携带7S和7.8S DNA连接酶的信息。