Novi A M, Baserga R
J Cell Biol. 1972 Dec;55(3):554-62. doi: 10.1083/jcb.55.3.554.
Chromatin template activity of mouse parotid glands increases after a single injection of isoproterenol (IPR), a procedure that causes, after a lag period of 20 hr, a marked stimulation of DNA synthesis and cell division in salivary glands of rodents. The increase in chromatin template activity occurs as early as 1 hr and peaks between 6 and 10 hr after IPR, paralleling previously reported changes in the incorporation of uridine-(3)H into total cellular RNA of mouse parotids. Template activity was measured in vitro in a system in which parotid gland chromatin was incubated with an exogenous RNA polymerase isolated from Escherichia coli. Similar results were obtained when template activity of parotid gland chromatin was assayed using an homologous RNA polymerase from mouse liver. Chromatin template activity in mouse parotids was also studied after the administration of drugs capable of inducing in salivary glands both DNA synthesis and secretion or secretion alone. The results indicate that the increased chromatin template activity occurring 6 hr after IPR is related to the subsequent onset of DNA synthesis. Furthermore, the increased chromatin template activity caused by IPR is inhibited by the previous administration of puromycin, an inhibitor of IPR-stimulated DNA synthesis.
单次注射异丙肾上腺素(IPR)后,小鼠腮腺的染色质模板活性会增加。在经过20小时的延迟期后,该操作会显著刺激啮齿动物唾液腺中的DNA合成和细胞分裂。染色质模板活性的增加最早在注射IPR后1小时出现,并在6至10小时达到峰值,这与先前报道的尿苷 -(3)H掺入小鼠腮腺总细胞RNA中的变化情况相似。在一个将腮腺染色质与从大肠杆菌中分离出的外源RNA聚合酶一起孵育的体外系统中测量模板活性。当使用来自小鼠肝脏的同源RNA聚合酶测定腮腺染色质的模板活性时,也得到了类似的结果。在给予能够诱导唾液腺中DNA合成和分泌或仅分泌的药物后,也对小鼠腮腺中的染色质模板活性进行了研究。结果表明,IPR后6小时出现的染色质模板活性增加与随后的DNA合成开始有关。此外,IPR引起的染色质模板活性增加会被先前给予的嘌呤霉素抑制,嘌呤霉素是一种抑制IPR刺激的DNA合成的抑制剂。