Yu F L
J Biol Chem. 1977 May 25;252(10):3245-51.
This paper reports the evidence for the existence of multiple sites of action of aflatoxin B1 in relation to its inhibition of rat hepatic nuclear RNA synthesis. Two hours after aflatoxin B1 injection (0.3 mg/100 g body weight), rat hepatic nuclear and nucleolar RNA synthesis, in vitro, were inhibited 70 and 90% respectively. When total nuclear free and engaged RNA polymerases were solubilized and assayed in the presence of alpha-amanitin (3.2 micrograms/ml), only alpha-amanitin-sensitive activity was reduced (50 to 70%) by aflatoxin B1. DEAE-Sephadex column chromatography confirmed this finding and further demonstrated that RNA polymerase II was the activity selectively inhibited. Since aflatoxin B1 dramatically inhibited nucleolar RNA synthesis, but had little effect on RNA polymerase I activity per se, it is concluded, therefore, that, in addition to its direct inhibitory effect on the enzymic function of RNA polymerase II, aflatoxin B1 must also cause impairment of the nucleolar DNA template function.
本文报道了黄曲霉毒素B1在抑制大鼠肝细胞核RNA合成方面存在多个作用位点的证据。注射黄曲霉毒素B1(0.3毫克/100克体重)两小时后,大鼠肝细胞核和核仁的RNA合成在体外分别被抑制了70%和90%。当在α-鹅膏蕈碱(3.2微克/毫升)存在的情况下溶解并测定总的游离和结合的核RNA聚合酶时,只有对α-鹅膏蕈碱敏感的活性被黄曲霉毒素B1降低了(50%至70%)。二乙氨基乙基葡聚糖柱色谱法证实了这一发现,并进一步表明RNA聚合酶II是被选择性抑制的活性。由于黄曲霉毒素B1显著抑制核仁RNA合成,但对RNA聚合酶I本身的活性影响很小,因此得出结论,除了对RNA聚合酶II的酶功能有直接抑制作用外,黄曲霉毒素B1还必定会导致核仁DNA模板功能受损。