Moyer G H, Gumbiner B, Austin G E
Department of Pathology, UCLA Center for the Health Sciences 90024.
Cancer Lett. 1977 Mar;2(4-5):259-65. doi: 10.1016/s0304-3835(77)80030-x.
The in vivo binding of N-hydroxy acetylaminofluorene (N-OH AAF) to rat liver DNA was studied in hetero- and euchromatin fractions prepared by sedimentation through sucrose gradients. The greater transcriptional capacity of the slowly sedimenting (euchromatin) fractions was confirmed by their enhanced incorporation of radioactive precursors into RNA in vivo and their increased template activity for in vitro RNA synthesis by purified RNA polymerase. N-OH AFF was bound in 4- to 5-fold greater amounts to euchromatin DNA than to heterochromatin 2 h after a single injection of the compound. However, the bound carcinogen appeared to be eliminated more rapidly from euchromatin than from heterochromatin by DNA repair processes.
通过蔗糖梯度沉降制备的异染色质和常染色质组分,研究了N-羟基乙酰氨基芴(N-OH AAF)在体内与大鼠肝脏DNA的结合。沉降较慢的(常染色质)组分具有较高的转录能力,这通过它们在体内将放射性前体增强掺入RNA以及它们对纯化的RNA聚合酶体外RNA合成的模板活性增加得到证实。单次注射该化合物2小时后,N-OH AFF与常染色质DNA的结合量比与异染色质的结合量高4至5倍。然而,通过DNA修复过程,结合的致癌物似乎从常染色质中比从异染色质中消除得更快。