Galbraith A, Itzhaki R F
Chem Biol Interact. 1979 Dec;28(2-3):309-22. doi: 10.1016/0009-2797(79)90171-6.
A study has been made of the histone and non-histone chromosomal proteins of rat liver after treatment in vivo with dimethylnitrosamine (DMN) (2 mg/kg). DMN was found not to affect histone turnover, as measured by 3H-labelled amino-acids incorporation. A decrease was observed in specific activity of the histones with time after injection of [14C]DMN or [14C]-formate and this was attributable to demethylation of both abnormal and normal methylation sites in these proteins. In the case of the non-histone proteins, DMN was found to increase greatly the turnover of those non-histone proteins loosely associated with chromatin DNA and RNA; turnover of those non-histone proteins tightly bound to chromatin DNA and RNA was unaffected. Demethylation of both normal and abnormal methylation sites was found to take place from both non-histone protein fractions. In the case of the loosely bound non-histone proteins a lower rate of demethylation was observed after DMN treatment.
对用二甲基亚硝胺(DMN)(2毫克/千克)进行体内处理后的大鼠肝脏组蛋白和非组蛋白染色体蛋白进行了一项研究。通过3H标记氨基酸掺入法测定发现,DMN不影响组蛋白周转。注射[14C]DMN或[14C] - 甲酸后,组蛋白的比活性随时间下降,这归因于这些蛋白质中异常和正常甲基化位点的去甲基化。对于非组蛋白,发现DMN大大增加了与染色质DNA和RNA松散结合的那些非组蛋白的周转;与染色质DNA和RNA紧密结合的那些非组蛋白的周转不受影响。发现正常和异常甲基化位点的去甲基化都发生在两个非组蛋白部分。对于松散结合的非组蛋白,DMN处理后观察到较低的去甲基化速率。