Abe Y, Cooper E, Spaulding S W
Endocrinology. 1982 Jun;110(6):2118-23. doi: 10.1210/endo-110-6-2118.
Little is known about the mechanisms of action of polypeptide hormones on chromatin structure and nuclear function. We have employed micrococcal nuclease to examine the effect of TSH on the accessibility of DNA in thyroid nuclei. Brief digestion of nuclear suspensions with 0.05-0.2 U/ml micrococcal nuclease at 26-28 C decreased their opacity at 600 nm. The decrease in opacity was linear with increasing nuclear concentration up to 0.2 mg/ml DNA. This response to nuclease was enhanced in nuclear suspensions prepared from thyroid slices that had been incubated with TSH (50 mU/ml) for 5 h (P less than 0.001). To determine whether TSH also increased the digestion of DNA, we measured the amount of DNA released into 1200 X g supernatants by nuclease treatment of nuclei prepared from control and TSH-treated slices. When TSH-treated nuclei (110 micrograms/100 microliters) were digested with 0.2 U micrococcal nuclease/ml at 37 C for 30 sec, a mean of 12.6 micrograms +/- 3.6 (SD) DNA appeared in the supernatant, as compared to 8.4 micrograms +/- 1.98 DNA from control nuclei (P less than 0.05). This increase in the insensitivity of nuclear DNA to micrococcal nuclease may reflect some conformational change in chromatin in response to TSH. Since micrococcal nuclease sensitivity may reflect transcriptional competence of DNA, we speculate that polypeptide hormones may enhance the accessibility of DNA to RNA polymerase or to endogenous stimulators of transcription.
关于多肽激素对染色质结构和核功能的作用机制,目前所知甚少。我们已采用微球菌核酸酶来研究促甲状腺激素(TSH)对甲状腺细胞核中DNA可及性的影响。在26 - 28℃下,用0.05 - 0.2 U/ml的微球菌核酸酶对核悬浮液进行短暂消化,可降低其在600 nm处的吸光度。吸光度的降低与核浓度增加呈线性关系,直至DNA浓度达到0.2 mg/ml。在用TSH(50 mU/ml)孵育5小时的甲状腺切片制备的核悬浮液中,对核酸酶的这种反应增强(P小于0.001)。为了确定TSH是否也增加了DNA的消化,我们测量了通过核酸酶处理对照和TSH处理切片制备的细胞核后,释放到1200×g上清液中的DNA量。当用0.2 U/ml的微球菌核酸酶在37℃下对TSH处理的细胞核(110微克/100微升)消化30秒时,上清液中平均出现12.6微克±3.6(标准差)的DNA,而对照细胞核的为8.4微克±1.98 DNA(P小于0.05)。核DNA对微球菌核酸酶不敏感性的这种增加可能反映了染色质响应TSH的某种构象变化。由于微球菌核酸酶敏感性可能反映DNA的转录活性,我们推测多肽激素可能增强DNA对RNA聚合酶或内源性转录刺激物的可及性。